PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
34516632-3	2022	Gata2 +9.5 deficiency removes the E-box motif and the GATA site and depletes fetal liver HSCs.	gata	54-58	GATA binding protein 2	Homo sapiens	0-5
32645737-10	2020	In conclusion, these findings suggest that cacao bean polyphenols prevent pressure overload-induced cardiac hypertrophy and systolic dysfunction by inhibiting the extracellular signal-regulated kinase 1/2-GATA binding protein 4 pathway in cardiomyocytes.	gata	205-209	brain expressed, associated with Nedd4, 1	Mus musculus	49-53
35500030-0	2022	The anterior Hox gene ceh-13 and elt-1/GATA activate the posterior Hox genes nob-1 and php-3 to specify posterior lineages in the C. elegans embryo.	gata	39-43	Transcription factor elt-1	Caenorhabditis elegans	33-38
35500030-0	2022	The anterior Hox gene ceh-13 and elt-1/GATA activate the posterior Hox genes nob-1 and php-3 to specify posterior lineages in the C. elegans embryo.	gata	39-43	Homeobox protein nob-1	Caenorhabditis elegans	77-82
35500030-0	2022	The anterior Hox gene ceh-13 and elt-1/GATA activate the posterior Hox genes nob-1 and php-3 to specify posterior lineages in the C. elegans embryo.	gata	39-43	Homeobox protein php-3	Caenorhabditis elegans	87-92
2535536-0	1989	ASF-2: a factor that binds to the cauliflower mosaic virus 35S promoter and a conserved GATA motif in Cab promoters.	gata	88-92	neural proliferation, differentiation and control 1	Homo sapiens	102-105
33624780-3	2021	Here, we show that mutations in the putative GATA-binding sites of the AVT4 promoter reduced AVT4 expression.	gata	45-49	Avt4p	Saccharomyces cerevisiae S288C	71-75
33624780-3	2021	Here, we show that mutations in the putative GATA-binding sites of the AVT4 promoter reduced AVT4 expression.	gata	45-49	Avt4p	Saccharomyces cerevisiae S288C	93-97
30523150-6	2019	ChIP results indicated that the TMG treatment decreases the occupancy of GATA-1, OGT, and OGA at the GATA-binding site of the lysosomal protein transmembrane 5 (Laptm5) gene promoter.	gata	73-77	lysosomal protein transmembrane 5	Homo sapiens	126-159
32823905-6	2020	The rs311103C disrupts the GATA-binding site, resulting in decreased CD99 expression.	gata	27-31	CD99 molecule (Xg blood group)	Homo sapiens	69-73
31440221-8	2019	This response is mainly regulated by a GATA transcription factor, most likely ELT-2, as indicated by the enrichment of (i) the GATA motif in the promoter regions of inducible genes and (ii) of ELT-2 targets among the differentially expressed genes.	gata	39-43	Transcription factor elt-2	Caenorhabditis elegans	78-83
31440221-8	2019	This response is mainly regulated by a GATA transcription factor, most likely ELT-2, as indicated by the enrichment of (i) the GATA motif in the promoter regions of inducible genes and (ii) of ELT-2 targets among the differentially expressed genes.	gata	39-43	Transcription factor elt-2	Caenorhabditis elegans	193-198
30818362-4	2019	Our data reveal Dal80 binding to a large set of promoters, sometimes independently of GATA sites, correlating with nitrogen- and/or Dal80-sensitive gene expression.	gata	86-90	Dal80p	Saccharomyces cerevisiae S288C	132-137
33073934-11	2020	In addition, the patient 3 who harboring missense variants in the GATA binding domain of TRPS1 showed more severe craniofacial and skeletal phenotypes.	gata	66-70	transcriptional repressor GATA binding 1	Homo sapiens	89-94
31520575-6	2019	AR binding sites (ARBS) are enriched for FOX, HOX, and GATA motifs in PC cells but not for c-JUN motifs in benign cells.	gata	55-59	androgen receptor	Homo sapiens	0-2
30914275-8	2019	Our findings, in addition to identifying the genetic cause of brachydactyly in two unrelated kindreds, emphasize the role of pathogenic TRPS1 variants in the development of brachydactyly type E and highlight the GATA DNA-binding region of TRPS1 protein with respect to phenotype-genotype correlation.	gata	212-216	transcriptional repressor GATA binding 1	Homo sapiens	239-244
30523150-6	2019	ChIP results indicated that the TMG treatment decreases the occupancy of GATA-1, OGT, and OGA at the GATA-binding site of the lysosomal protein transmembrane 5 (Laptm5) gene promoter.	gata	73-77	lysosomal protein transmembrane 5	Homo sapiens	161-167
29550363-5	2018	In the present study, we revealed the dynamics of Gata.a and beta-catenin, and expression profiles of their target genes precisely.	gata	50-54	beta-catenin	Ciona intestinalis	61-73
30315105-5	2018	Mechanistically, TRPS1 repressed SOX2 expression by directly targeting the consensus GATA-binding element in the SOX2 promoter as elucidated by ChIP and luciferase reporter assays.	gata	85-89	transcriptional repressor GATA binding 1	Mus musculus	17-22
30315105-5	2018	Mechanistically, TRPS1 repressed SOX2 expression by directly targeting the consensus GATA-binding element in the SOX2 promoter as elucidated by ChIP and luciferase reporter assays.	gata	85-89	SRY (sex determining region Y)-box 2	Mus musculus	33-37
30315105-5	2018	Mechanistically, TRPS1 repressed SOX2 expression by directly targeting the consensus GATA-binding element in the SOX2 promoter as elucidated by ChIP and luciferase reporter assays.	gata	85-89	SRY (sex determining region Y)-box 2	Mus musculus	113-117
30510588-6	2018	Additionally, DNA methylation was also altered by TCS exposure, especially in those regions with GATA motif enrichment.	gata	97-101	treacle ribosome biogenesis factor 1	Homo sapiens	50-53
29991720-7	2018	We demonstrate that RUNX1 induction moves FLI1 from distal ETS/GATA sites to RUNX1/ETS sites and recruits the basal transcription factors CDK9, BRD4, the Mediator complex and the looping factor LDB1.	gata	63-67	runt related transcription factor 1	Mus musculus	20-25
29991720-7	2018	We demonstrate that RUNX1 induction moves FLI1 from distal ETS/GATA sites to RUNX1/ETS sites and recruits the basal transcription factors CDK9, BRD4, the Mediator complex and the looping factor LDB1.	gata	63-67	Friend leukemia integration 1	Mus musculus	42-46
29991720-7	2018	We demonstrate that RUNX1 induction moves FLI1 from distal ETS/GATA sites to RUNX1/ETS sites and recruits the basal transcription factors CDK9, BRD4, the Mediator complex and the looping factor LDB1.	gata	63-67	cyclin-dependent kinase 9 (CDC2-related kinase)	Mus musculus	138-142
29991720-7	2018	We demonstrate that RUNX1 induction moves FLI1 from distal ETS/GATA sites to RUNX1/ETS sites and recruits the basal transcription factors CDK9, BRD4, the Mediator complex and the looping factor LDB1.	gata	63-67	bromodomain containing 4	Mus musculus	144-148
29991720-7	2018	We demonstrate that RUNX1 induction moves FLI1 from distal ETS/GATA sites to RUNX1/ETS sites and recruits the basal transcription factors CDK9, BRD4, the Mediator complex and the looping factor LDB1.	gata	63-67	LIM domain binding 1	Mus musculus	194-198
29197504-5	2018	Both sequences contain GATA binding motifs, and expression pattern analysis identified that Gata6 is expressed in the flank and the anterior portion of nascent hindlimb buds.	gata	23-27	GATA binding protein 6	Mus musculus	92-97
29263149-7	2018	We also demonstrate that Pdx1 expression in adult beta-cells depends on GATA sites in transgenic reporter mice and that loss of GATA6 greatly affects beta-cell-specific gene expression.	gata	72-76	pancreatic and duodenal homeobox 1	Mus musculus	25-29
29564399-6	2018	For example, the core GATA activators GAT1 and GLN3 have a conserved role in nitrogen catabolite repression (NCR).	gata	22-26	Gat1p	Saccharomyces cerevisiae S288C	38-42
29564399-6	2018	For example, the core GATA activators GAT1 and GLN3 have a conserved role in nitrogen catabolite repression (NCR).	gata	22-26	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	47-51
28082341-8	2017	Chromatin immunoprecipitation sequencing revealed 5 GATA binding sites in a regulatory region 31 kb upstream of NBEAL2 covered by a H3K4Me1 mark indicative of an enhancer locus.	gata	52-56	neurobeachin like 2	Homo sapiens	112-118
29299165-11	2017	Chromatin immunoprecipitation (ChIP) assays validated that GATA3 binds directly to the +220 GATA binding motif on the human vWF promoter and A549 conditioned media significantly increases the binding of GATA3.	gata	59-63	von Willebrand factor	Homo sapiens	124-127
29299165-11	2017	Chromatin immunoprecipitation (ChIP) assays validated that GATA3 binds directly to the +220 GATA binding motif on the human vWF promoter and A549 conditioned media significantly increases the binding of GATA3.	gata	59-63	GATA binding protein 3	Homo sapiens	203-208
28216155-6	2017	Promoter analysis and quantitative ChIP analysis demonstrated that FOG1-mediated transcriptional repression of PU.1 would be mediated through a GATA-binding element located at its promoter, accompanied by significantly decreased H3 acetylation at lysine 4 and 9 (K4 and K9) as well as H3K4 trimethylation.	gata	144-148	zinc finger protein, FOG family member 1	Homo sapiens	67-71
28216155-6	2017	Promoter analysis and quantitative ChIP analysis demonstrated that FOG1-mediated transcriptional repression of PU.1 would be mediated through a GATA-binding element located at its promoter, accompanied by significantly decreased H3 acetylation at lysine 4 and 9 (K4 and K9) as well as H3K4 trimethylation.	gata	144-148	Spi-1 proto-oncogene	Homo sapiens	111-115
29035278-5	2017	In response to oscillatory shear stress, the transcription factors Tal1, Gata2, and Ets1/2 physically interacted with and recruited Hdac3 to the evolutionarily conserved E-box-GATA-ETS composite element of a Gata2 intragenic enhancer.	gata	176-180	T cell acute lymphocytic leukemia 1	Mus musculus	67-71
29035278-5	2017	In response to oscillatory shear stress, the transcription factors Tal1, Gata2, and Ets1/2 physically interacted with and recruited Hdac3 to the evolutionarily conserved E-box-GATA-ETS composite element of a Gata2 intragenic enhancer.	gata	176-180	GATA binding protein 2	Mus musculus	73-78
29035278-5	2017	In response to oscillatory shear stress, the transcription factors Tal1, Gata2, and Ets1/2 physically interacted with and recruited Hdac3 to the evolutionarily conserved E-box-GATA-ETS composite element of a Gata2 intragenic enhancer.	gata	176-180	E26 avian leukemia oncogene 1, 5' domain	Mus musculus	84-88
29035278-5	2017	In response to oscillatory shear stress, the transcription factors Tal1, Gata2, and Ets1/2 physically interacted with and recruited Hdac3 to the evolutionarily conserved E-box-GATA-ETS composite element of a Gata2 intragenic enhancer.	gata	176-180	histone deacetylase 3	Mus musculus	132-137
29035278-5	2017	In response to oscillatory shear stress, the transcription factors Tal1, Gata2, and Ets1/2 physically interacted with and recruited Hdac3 to the evolutionarily conserved E-box-GATA-ETS composite element of a Gata2 intragenic enhancer.	gata	176-180	GATA binding protein 2	Mus musculus	208-213
28982936-6	2017	The AP1 site also serves as a GATA-binding site in one of the bovine IFNT genes.	gata	30-34	Jun proto-oncogene, AP-1 transcription factor subunit	Bos taurus	4-7
28982936-6	2017	The AP1 site also serves as a GATA-binding site in one of the bovine IFNT genes.	gata	30-34	interferon-tau 3g	Bos taurus	69-73
28007891-1	2017	Nitrogen catabolite repression (NCR), the ability of Saccharomyces cerevisiae to use good nitrogen sources in preference to poor ones, derives from nitrogen-responsive regulation of the GATA family transcription activators Gln3 and Gat1 In nitrogen-replete conditions, the GATA factors are cytoplasmic and NCR-sensitive transcription minimal.	gata	186-190	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	223-227
27746176-7	2017	These data suggest that GATA factor could affect G protein signaling through regulating RGS4 expression, and GATA signaling may develop as a future therapeutic target for RGS4-related diseases.	gata	24-28	regulator of G-protein signaling 4	Oryctolagus cuniculus	88-92
27746176-7	2017	These data suggest that GATA factor could affect G protein signaling through regulating RGS4 expression, and GATA signaling may develop as a future therapeutic target for RGS4-related diseases.	gata	24-28	regulator of G-protein signaling 4	Oryctolagus cuniculus	171-175
28007891-1	2017	Nitrogen catabolite repression (NCR), the ability of Saccharomyces cerevisiae to use good nitrogen sources in preference to poor ones, derives from nitrogen-responsive regulation of the GATA family transcription activators Gln3 and Gat1 In nitrogen-replete conditions, the GATA factors are cytoplasmic and NCR-sensitive transcription minimal.	gata	186-190	Gat1p	Saccharomyces cerevisiae S288C	232-236
28007891-1	2017	Nitrogen catabolite repression (NCR), the ability of Saccharomyces cerevisiae to use good nitrogen sources in preference to poor ones, derives from nitrogen-responsive regulation of the GATA family transcription activators Gln3 and Gat1 In nitrogen-replete conditions, the GATA factors are cytoplasmic and NCR-sensitive transcription minimal.	gata	273-277	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	223-227
28007891-1	2017	Nitrogen catabolite repression (NCR), the ability of Saccharomyces cerevisiae to use good nitrogen sources in preference to poor ones, derives from nitrogen-responsive regulation of the GATA family transcription activators Gln3 and Gat1 In nitrogen-replete conditions, the GATA factors are cytoplasmic and NCR-sensitive transcription minimal.	gata	273-277	Gat1p	Saccharomyces cerevisiae S288C	232-236
27231347-1	2016	One mode of gamma-globin gene silencing involves a GATA-1 FOG-1 Mi2beta repressor complex that binds to the -566 GATA site relative to the (A)gamma-globin gene cap site.	gata	51-55	chromodomain helicase DNA binding protein 4	Homo sapiens	64-71
28123038-0	2017	Intron 1 GATA site enhances ALAS2 expression indispensably during erythroid differentiation.	gata	9-13	aminolevulinic acid synthase 2, erythroid	Mus musculus	28-33
28123038-1	2017	The first intronic mutations in the intron 1 GATA site (int-1-GATA) of 5-aminolevulinate synthase 2 (ALAS2) have been identified in X-linked sideroblastic anemia (XLSA) pedigrees, strongly suggesting it could be causal mutations of XLSA.	gata	45-49	wingless-type MMTV integration site family, member 1	Mus musculus	56-61
28123038-1	2017	The first intronic mutations in the intron 1 GATA site (int-1-GATA) of 5-aminolevulinate synthase 2 (ALAS2) have been identified in X-linked sideroblastic anemia (XLSA) pedigrees, strongly suggesting it could be causal mutations of XLSA.	gata	45-49	aminolevulinic acid synthase 2, erythroid	Mus musculus	71-99
28123038-1	2017	The first intronic mutations in the intron 1 GATA site (int-1-GATA) of 5-aminolevulinate synthase 2 (ALAS2) have been identified in X-linked sideroblastic anemia (XLSA) pedigrees, strongly suggesting it could be causal mutations of XLSA.	gata	45-49	aminolevulinic acid synthase 2, erythroid	Mus musculus	101-106
28123038-2	2017	However, the function of this int-1-GATA site during in vivo development remains largely unknown.	gata	36-40	wingless-type MMTV integration site family, member 1	Mus musculus	30-35
27231347-7	2016	Taken together, our data suggest that O-GlcNAcylation is a novel mechanism of gamma-globin gene regulation mediated by modulating the assembly of the GATA-1 FOG-1 Mi2beta repressor complex at the -566 GATA motif within the promoter.	gata	150-154	zinc finger protein, FOG family member 1	Homo sapiens	157-162
27231347-7	2016	Taken together, our data suggest that O-GlcNAcylation is a novel mechanism of gamma-globin gene regulation mediated by modulating the assembly of the GATA-1 FOG-1 Mi2beta repressor complex at the -566 GATA motif within the promoter.	gata	150-154	chromodomain helicase DNA binding protein 4	Homo sapiens	163-170
27231347-1	2016	One mode of gamma-globin gene silencing involves a GATA-1 FOG-1 Mi2beta repressor complex that binds to the -566 GATA site relative to the (A)gamma-globin gene cap site.	gata	51-55	hemoglobin subunit gamma 1	Homo sapiens	140-154
27231347-3	2016	In this study, we demonstrate that the O-linked N-acetylglucosamine (O-GlcNAc) processing enzymes, O-GlcNAc-transferase (OGT) and O-GlcNAcase (OGA), interact with the (A)gamma-globin promoter at the -566 GATA repressor site; however, mutation of the GATA site to GAGA significantly reduces OGT and OGA promoter interactions in beta-globin locus yeast artificial chromosome (beta-YAC) bone marrow cells.	gata	204-208	O-linked N-acetylglucosamine (GlcNAc) transferase	Homo sapiens	69-77
27231347-3	2016	In this study, we demonstrate that the O-linked N-acetylglucosamine (O-GlcNAc) processing enzymes, O-GlcNAc-transferase (OGT) and O-GlcNAcase (OGA), interact with the (A)gamma-globin promoter at the -566 GATA repressor site; however, mutation of the GATA site to GAGA significantly reduces OGT and OGA promoter interactions in beta-globin locus yeast artificial chromosome (beta-YAC) bone marrow cells.	gata	204-208	O-linked N-acetylglucosamine (GlcNAc) transferase	Homo sapiens	99-107
27231347-3	2016	In this study, we demonstrate that the O-linked N-acetylglucosamine (O-GlcNAc) processing enzymes, O-GlcNAc-transferase (OGT) and O-GlcNAcase (OGA), interact with the (A)gamma-globin promoter at the -566 GATA repressor site; however, mutation of the GATA site to GAGA significantly reduces OGT and OGA promoter interactions in beta-globin locus yeast artificial chromosome (beta-YAC) bone marrow cells.	gata	204-208	O-linked N-acetylglucosamine (GlcNAc) transferase	Homo sapiens	121-124
27231347-3	2016	In this study, we demonstrate that the O-linked N-acetylglucosamine (O-GlcNAc) processing enzymes, O-GlcNAc-transferase (OGT) and O-GlcNAcase (OGA), interact with the (A)gamma-globin promoter at the -566 GATA repressor site; however, mutation of the GATA site to GAGA significantly reduces OGT and OGA promoter interactions in beta-globin locus yeast artificial chromosome (beta-YAC) bone marrow cells.	gata	204-208	O-GlcNAcase	Homo sapiens	130-141
27231347-3	2016	In this study, we demonstrate that the O-linked N-acetylglucosamine (O-GlcNAc) processing enzymes, O-GlcNAc-transferase (OGT) and O-GlcNAcase (OGA), interact with the (A)gamma-globin promoter at the -566 GATA repressor site; however, mutation of the GATA site to GAGA significantly reduces OGT and OGA promoter interactions in beta-globin locus yeast artificial chromosome (beta-YAC) bone marrow cells.	gata	204-208	O-GlcNAcase	Homo sapiens	143-146
27231347-3	2016	In this study, we demonstrate that the O-linked N-acetylglucosamine (O-GlcNAc) processing enzymes, O-GlcNAc-transferase (OGT) and O-GlcNAcase (OGA), interact with the (A)gamma-globin promoter at the -566 GATA repressor site; however, mutation of the GATA site to GAGA significantly reduces OGT and OGA promoter interactions in beta-globin locus yeast artificial chromosome (beta-YAC) bone marrow cells.	gata	204-208	hemoglobin subunit gamma 1	Homo sapiens	168-182
27231347-3	2016	In this study, we demonstrate that the O-linked N-acetylglucosamine (O-GlcNAc) processing enzymes, O-GlcNAc-transferase (OGT) and O-GlcNAcase (OGA), interact with the (A)gamma-globin promoter at the -566 GATA repressor site; however, mutation of the GATA site to GAGA significantly reduces OGT and OGA promoter interactions in beta-globin locus yeast artificial chromosome (beta-YAC) bone marrow cells.	gata	204-208	O-linked N-acetylglucosamine (GlcNAc) transferase	Homo sapiens	290-293
27231347-3	2016	In this study, we demonstrate that the O-linked N-acetylglucosamine (O-GlcNAc) processing enzymes, O-GlcNAc-transferase (OGT) and O-GlcNAcase (OGA), interact with the (A)gamma-globin promoter at the -566 GATA repressor site; however, mutation of the GATA site to GAGA significantly reduces OGT and OGA promoter interactions in beta-globin locus yeast artificial chromosome (beta-YAC) bone marrow cells.	gata	204-208	O-GlcNAcase	Homo sapiens	298-301
27152625-7	2016	Third, Gata.a directs specific gene expression in the animal hemisphere domain, because beta-catenin/Tcf7 weakens the Gata.a-binding activity for target sites through a physical interaction in the vegetal cells.	gata	7-11	beta-catenin	Ciona intestinalis	88-100
27079877-6	2016	Using a combination of targeted mutagenesis of transcription factor-binding sites and gene silencing of transcription factors, we found that Gata and Ets factors are required for Flk1in10 enhancer activity in all endothelial cells.	gata	141-145	kinase insert domain protein receptor	Mus musculus	179-183
27340386-2	2016	The regulatory sequence of the CCR3 gene, contains two Runt-related transcription factor (RUNX) 1 sites and two PU.1 sites, in addition to a functional GATA site for transactivation of the CCR3 gene.	gata	152-156	C-C motif chemokine receptor 3	Homo sapiens	31-35
27340386-2	2016	The regulatory sequence of the CCR3 gene, contains two Runt-related transcription factor (RUNX) 1 sites and two PU.1 sites, in addition to a functional GATA site for transactivation of the CCR3 gene.	gata	152-156	C-C motif chemokine receptor 3	Homo sapiens	189-193
27152625-7	2016	Third, Gata.a directs specific gene expression in the animal hemisphere domain, because beta-catenin/Tcf7 weakens the Gata.a-binding activity for target sites through a physical interaction in the vegetal cells.	gata	118-122	beta-catenin	Ciona intestinalis	88-100
26896592-0	2016	Mutagenesis of GATA motifs controlling the endoderm regulator elt-2 reveals distinct dominant and secondary cis-regulatory elements.	gata	15-19	Transcription factor elt-2	Caenorhabditis elegans	62-67
26896592-5	2016	We determined that a single primary dominant GATA motif located 527bp upstream of the elt-2 start codon was necessary for both embryonic activation and later maintenance of transcription, while nearby secondary GATA motifs played largely subtle roles in modulating postembryonic levels of elt-2.	gata	45-49	Transcription factor elt-2	Caenorhabditis elegans	86-91
25938608-7	2015	In 293T gel shift assays, exogenous C/EBPalpha binds both C/EBP sites, c-Myb binds the Myb site, PU.1 binds the second Ets site, PU.1, Fli-1, ERG, and Ets1 bind the sixth Ets site, GATA2 binds both GATA sites, and SCL binds the second E-box.	gata	181-185	CCAAT/enhancer binding protein (C/EBP), alpha	Mus musculus	36-46
26932670-6	2016	Consistent with the erroneous activation of hedgehog signaling, we demonstrate that GATA4 and GATA6 are able to repress transcription through the sonic hedgehog (Shh) endoderm-specific enhancer MACS1 and that GATA-binding sites within this enhancer are necessary for this repressive activity.	gata	84-88	sonic hedgehog signaling molecule	Homo sapiens	146-160
26932670-6	2016	Consistent with the erroneous activation of hedgehog signaling, we demonstrate that GATA4 and GATA6 are able to repress transcription through the sonic hedgehog (Shh) endoderm-specific enhancer MACS1 and that GATA-binding sites within this enhancer are necessary for this repressive activity.	gata	84-88	sonic hedgehog signaling molecule	Homo sapiens	162-165
26932670-6	2016	Consistent with the erroneous activation of hedgehog signaling, we demonstrate that GATA4 and GATA6 are able to repress transcription through the sonic hedgehog (Shh) endoderm-specific enhancer MACS1 and that GATA-binding sites within this enhancer are necessary for this repressive activity.	gata	84-88	acyl-CoA synthetase medium chain family member 1	Homo sapiens	194-199
25825272-8	2015	Claudin-2 has hyperosmolarity-sensitive region in its promoter, which includes GATA binding site.	gata	79-83	claudin 2	Canis lupus familiaris	0-9
26601269-3	2015	Mutation of an intronic GATA motif (+9.5) in GATA2, encoding a master regulator of hematopoiesis, underlies an immunodeficiency associated with myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML).	gata	24-28	GATA binding protein 2	Mus musculus	45-50
26183398-3	2015	We identified TRPS1 (tricho-rhino-phalangeal-syndrome 1), a repressor of GATA-mediated transcription, and BAT3 (Scythe/BAG6), a nucleo-cytoplasmic shuttling chaperone protein, as new Cath-D-interacting nuclear proteins.	gata	73-77	transcriptional repressor GATA binding 1	Homo sapiens	21-55
25938608-7	2015	In 293T gel shift assays, exogenous C/EBPalpha binds both C/EBP sites, c-Myb binds the Myb site, PU.1 binds the second Ets site, PU.1, Fli-1, ERG, and Ets1 bind the sixth Ets site, GATA2 binds both GATA sites, and SCL binds the second E-box.	gata	181-185	CCAAT/enhancer binding protein (C/EBP), alpha	Mus musculus	36-41
24018543-0	2013	GATA augments GNRH-mediated increases in Adcyap1 gene expression in pituitary gonadotrope cells.	gata	0-4	gonadotropin releasing hormone 1	Rattus norvegicus	14-18
25552417-9	2015	Of note, PIAS1 depletion affected AR chromatin occupancy at binding sites enriched for HOXD13 and GATA motifs.	gata	98-102	protein inhibitor of activated STAT 1	Homo sapiens	9-14
25552417-9	2015	Of note, PIAS1 depletion affected AR chromatin occupancy at binding sites enriched for HOXD13 and GATA motifs.	gata	98-102	androgen receptor	Homo sapiens	34-36
25429295-8	2014	This common regulatory framework comprises a composite box made of the GATA motifs and GCN4-like Motifs (GLMs) and was shown to be functional as the GLMs are able to bind a bZIP transcriptional factor SPA (Storage Protein Activator).	gata	71-75	bZIP transcription factor RISBZ2	Triticum aestivum	201-204
25429295-8	2014	This common regulatory framework comprises a composite box made of the GATA motifs and GCN4-like Motifs (GLMs) and was shown to be functional as the GLMs are able to bind a bZIP transcriptional factor SPA (Storage Protein Activator).	gata	71-75	bZIP transcription factor RISBZ2	Triticum aestivum	206-231
24166784-0	2014	X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations.	gata	69-73	5'-aminolevulinate synthase 2	Homo sapiens	37-42
25675838-6	2015	Additionally, we found evidence of interspecies variation in binding sites for several regulatory elements linked to iNOS (GATA-3, GATA-4, KLF6, SRF, STAT-1, STAT-3, OLF-1 and HIF-1) across species, especially in African green monkeys relative to other species.	gata	123-127	nitric oxide synthase 2	Macaca mulatta	117-121
25711168-8	2015	Finally, we provide evidence that col-41 expression is controlled by a sequence element containing two GATA sites and by the epidermal GATA transcription factors ELT-1 and ELT-3.	gata	103-107	Col_cuticle_N domain-containing protein	Caenorhabditis elegans	34-40
26430560-0	2015	The C. elegans embryonic fate specification factor EGL-18 (GATA) is reutilized downstream of Wnt signaling to maintain a population of larval progenitor cells.	gata	59-63	GATA-type domain-containing protein	Caenorhabditis elegans	51-57
24636993-7	2014	We introduced biotin-tagged GATA2 into a mouse CD-derived cell line and conducted chromatin pulldown assays, which revealed direct GATA2 binding to conserved GATA motifs in the Aqp2 promoter region.	gata	28-32	GATA binding protein 2	Mus musculus	131-136
24636993-7	2014	We introduced biotin-tagged GATA2 into a mouse CD-derived cell line and conducted chromatin pulldown assays, which revealed direct GATA2 binding to conserved GATA motifs in the Aqp2 promoter region.	gata	28-32	aquaporin 2	Mus musculus	177-181
24636993-8	2014	A luciferase reporter assay using an Aqp2 promoter-reporter showed that GATA2 trans activates Aqp2 through the GATA motifs.	gata	72-76	aquaporin 2	Mus musculus	37-41
24636993-8	2014	A luciferase reporter assay using an Aqp2 promoter-reporter showed that GATA2 trans activates Aqp2 through the GATA motifs.	gata	72-76	aquaporin 2	Mus musculus	94-98
23935018-6	2014	Importantly, two mutations, each of which disrupts the GATA-binding site in the enhancer, were identified in unrelated male patients with congenital sideroblastic anemia, and the lower expression level of ALAS2 mRNA in bone marrow erythroblasts was confirmed in one of these patients.	gata	55-59	5'-aminolevulinate synthase 2	Homo sapiens	205-210
24018543-0	2013	GATA augments GNRH-mediated increases in Adcyap1 gene expression in pituitary gonadotrope cells.	gata	0-4	adenylate cyclase activating polypeptide 1	Rattus norvegicus	41-48
24018543-5	2013	By transient transfection and electrophoretic mobility shift assay analysis, we demonstrate that GATA2 and GATA4 stimulate Adcyap1 promoter activity via a GATA cis-element located at position -191 in the rat Adcyap1 gene promoter.	gata	97-101	adenylate cyclase activating polypeptide 1	Rattus norvegicus	123-130
24021675-8	2013	The 3.2-kb sequences interspaced between the Gata1 hematopoietic enhancer and the double GATA-motif were able to recruit DNA methyltransferase 1, thereby exerting a cis-repressive function in the HSC-like cell line.	gata	89-93	GATA binding protein 1	Homo sapiens	45-50
24021675-8	2013	The 3.2-kb sequences interspaced between the Gata1 hematopoietic enhancer and the double GATA-motif were able to recruit DNA methyltransferase 1, thereby exerting a cis-repressive function in the HSC-like cell line.	gata	89-93	DNA methyltransferase 1	Homo sapiens	121-144
24018543-5	2013	By transient transfection and electrophoretic mobility shift assay analysis, we demonstrate that GATA2 and GATA4 stimulate Adcyap1 promoter activity via a GATA cis-element located at position -191 in the rat Adcyap1 gene promoter.	gata	97-101	adenylate cyclase activating polypeptide 1	Rattus norvegicus	208-215
24018543-7	2013	Conversely, blunting GATA expression with specific siRNA inhibits the ability of GNRH to stimulate ADCYAP1 mRNA levels in these cells.	gata	21-25	gonadotropin releasing hormone 1	Rattus norvegicus	81-85
24018543-7	2013	Conversely, blunting GATA expression with specific siRNA inhibits the ability of GNRH to stimulate ADCYAP1 mRNA levels in these cells.	gata	21-25	adenylate cyclase activating polypeptide 1	Rattus norvegicus	99-106
24006283-8	2013	Mutation studies identified the minimal region conferring basal and forskolin-stimulated VNN2 promoter activities, which were dependent on chicken ovalbumin upstream promoter-transcription factor (COUP-TF), GATA, and Ebox cis-elements.	gata	207-211	vanin 2	Gallus gallus	89-93
24112087-9	2013	Site-directed mutagenesis in transcription-factor-binding sites, including Ets, GATA, and AP2, verified their key roles in regulating transcription, especially sites Ets (-103), GATA (-211), and AP2 (-3).	gata	80-84	transcription factor AP-2 beta	Sus scrofa	195-198
24112087-9	2013	Site-directed mutagenesis in transcription-factor-binding sites, including Ets, GATA, and AP2, verified their key roles in regulating transcription, especially sites Ets (-103), GATA (-211), and AP2 (-3).	gata	178-182	transcription factor AP-2 beta	Sus scrofa	90-93
23874392-4	2013	The promoter region of SLCO4C1 gene has several GATA motifs, and indoxyl sulfate up-regulated GATA3 mRNA and subsequently down-regulated SLCO4C1 mRNA.	gata	48-52	solute carrier organic anion transporter family, member 4C1	Rattus norvegicus	23-30
23183747-3	2013	A potentially functional polymorphism (i.e., rs4938723T/C) in the promoter region of pri-miR-34b/c was predicted to influence the GATA-X binding sites.	gata	130-134	microRNA 34b	Homo sapiens	89-96
23717578-5	2013	Runx1 occupied genomic regions were highly enriched in RUNX and ETS motifs and to a lesser extent in GATA motif.	gata	101-105	runt related transcription factor 1	Mus musculus	0-5
23211524-9	2013	The trans-repressive action of GATA2 on Gnrhr promoter activity is likely balanced or even hindered by trans-activating effects of LIM homeodomain proteins via this novel bifunctional LIM/GATA response element.	gata	31-35	gonadotropin releasing hormone receptor	Mus musculus	40-45
23325760-3	2013	Many of the identified Notch-regulated enhancers contain Runx and GATA motifs, and we demonstrate that binding of the Runx protein Lozenge (Lz) is required for enhancers to be competent to respond to Notch.	gata	66-70	Notch	Drosophila melanogaster	23-28
23325760-3	2013	Many of the identified Notch-regulated enhancers contain Runx and GATA motifs, and we demonstrate that binding of the Runx protein Lozenge (Lz) is required for enhancers to be competent to respond to Notch.	gata	66-70	lozenge	Drosophila melanogaster	131-138
23325760-3	2013	Many of the identified Notch-regulated enhancers contain Runx and GATA motifs, and we demonstrate that binding of the Runx protein Lozenge (Lz) is required for enhancers to be competent to respond to Notch.	gata	66-70	Notch	Drosophila melanogaster	200-205
23085565-6	2012	Moreover, we determined the effect of tanshinone IIA on IRF-1 or GATAs induction and binding activity to VCAM-1 promoter since the upstream promoter region of VCAM-1 but not ICAM-1 contains IRF-1 and GATA binding motifs.	gata	65-69	vascular cell adhesion molecule 1	Homo sapiens	159-165
22996659-3	2012	Though the disease-causing mutations commonly occur in the GATA-2 DNA binding domain, we identified a patient with mycobacterial infection and myelodysplasia who had an uncharacterized heterozygous deletion in a GATA2 cis-element consisting of an E-box and a GATA motif.	gata	59-63	GATA binding protein 2	Homo sapiens	212-217
22996659-3	2012	Though the disease-causing mutations commonly occur in the GATA-2 DNA binding domain, we identified a patient with mycobacterial infection and myelodysplasia who had an uncharacterized heterozygous deletion in a GATA2 cis-element consisting of an E-box and a GATA motif.	gata	59-63	cytokine inducible SH2 containing protein	Homo sapiens	218-221
22420414-7	2012	Consistent with their expression patterns during chick embryonic development, Gata4, Nanog and Ets1 are recruited on the LTR in embryonic stem cells; in the epiblast the complementary expression of Nanog and Gata/Ets correlates with the Ens-1 gene expression pattern; and Ens-1 transcripts are also detected in the hypoblast, an extraembryonic tissue expressing Gata4 and Ets2, but not Nanog.	gata	78-82	Nanog homeobox	Gallus gallus	198-203
22867996-6	2012	Functional analysis of the HELIOS-BCL11B fusion protein revealed reduced transcriptional suppression activity compared to that of the WT-BCL11B due to the loss of the N-terminal friend of GATA-repression motif, which functions as a metastasis-associated protein 2 binding site.	gata	188-192	IKAROS family zinc finger 2	Homo sapiens	27-33
22867996-6	2012	Functional analysis of the HELIOS-BCL11B fusion protein revealed reduced transcriptional suppression activity compared to that of the WT-BCL11B due to the loss of the N-terminal friend of GATA-repression motif, which functions as a metastasis-associated protein 2 binding site.	gata	188-192	BAF chromatin remodeling complex subunit BCL11B	Homo sapiens	34-40
22867996-6	2012	Functional analysis of the HELIOS-BCL11B fusion protein revealed reduced transcriptional suppression activity compared to that of the WT-BCL11B due to the loss of the N-terminal friend of GATA-repression motif, which functions as a metastasis-associated protein 2 binding site.	gata	188-192	BAF chromatin remodeling complex subunit BCL11B	Homo sapiens	137-143
22525679-4	2012	The quality of the carbon source modulates UGA4 expression through two parallel pathways, each one acting on different regulatory elements, the UAS(GATA) and the UAS(GABA).	gata	148-152	Uga4p	Saccharomyces cerevisiae S288C	43-47
22865859-5	2012	Reporter assays suggested that two GATA motifs just upstream of the transcription start site in the ST2 promoter are critical for transcriptional activity.	gata	35-39	ST2	Homo sapiens	100-103
22865859-6	2012	These two GATA motifs possess the capacity to bind GATA1 and GATA2 in EMSA.	gata	10-14	GATA binding protein 1	Homo sapiens	51-56
22865859-6	2012	These two GATA motifs possess the capacity to bind GATA1 and GATA2 in EMSA.	gata	10-14	GATA binding protein 2	Homo sapiens	61-66
22422726-6	2012	Using luciferase reporter analysis in rat cardiomyocytes, it can be shown that MEF2, GATA, and E-box regulatory elements are essential for efficient expression of the Myh7b gene.	gata	85-89	myosin heavy chain 7B	Rattus norvegicus	167-172
22420414-7	2012	Consistent with their expression patterns during chick embryonic development, Gata4, Nanog and Ets1 are recruited on the LTR in embryonic stem cells; in the epiblast the complementary expression of Nanog and Gata/Ets correlates with the Ens-1 gene expression pattern; and Ens-1 transcripts are also detected in the hypoblast, an extraembryonic tissue expressing Gata4 and Ets2, but not Nanog.	gata	78-82	ENS-1	Gallus gallus	237-242
22420414-7	2012	Consistent with their expression patterns during chick embryonic development, Gata4, Nanog and Ets1 are recruited on the LTR in embryonic stem cells; in the epiblast the complementary expression of Nanog and Gata/Ets correlates with the Ens-1 gene expression pattern; and Ens-1 transcripts are also detected in the hypoblast, an extraembryonic tissue expressing Gata4 and Ets2, but not Nanog.	gata	78-82	ENS-1	Gallus gallus	272-277
22420414-7	2012	Consistent with their expression patterns during chick embryonic development, Gata4, Nanog and Ets1 are recruited on the LTR in embryonic stem cells; in the epiblast the complementary expression of Nanog and Gata/Ets correlates with the Ens-1 gene expression pattern; and Ens-1 transcripts are also detected in the hypoblast, an extraembryonic tissue expressing Gata4 and Ets2, but not Nanog.	gata	78-82	GATA binding protein 4	Gallus gallus	362-367
22420414-7	2012	Consistent with their expression patterns during chick embryonic development, Gata4, Nanog and Ets1 are recruited on the LTR in embryonic stem cells; in the epiblast the complementary expression of Nanog and Gata/Ets correlates with the Ens-1 gene expression pattern; and Ens-1 transcripts are also detected in the hypoblast, an extraembryonic tissue expressing Gata4 and Ets2, but not Nanog.	gata	78-82	ETS proto-oncogene 2, transcription factor	Gallus gallus	372-376
22420414-7	2012	Consistent with their expression patterns during chick embryonic development, Gata4, Nanog and Ets1 are recruited on the LTR in embryonic stem cells; in the epiblast the complementary expression of Nanog and Gata/Ets correlates with the Ens-1 gene expression pattern; and Ens-1 transcripts are also detected in the hypoblast, an extraembryonic tissue expressing Gata4 and Ets2, but not Nanog.	gata	78-82	Nanog homeobox	Gallus gallus	198-203
22420414-10	2012	By providing pluripotent cells with intact binding sites for Gata, Nanog, or both, Ens-1 LTR may promote distinct transcriptional networks in embryonic stem cells subpopulations and prime the separation between embryonic and extraembryonic fates.	gata	61-65	ENS-1	Gallus gallus	83-88
22071109-7	2011	The enhancer is activated by Bmp, Wnt and Fgf, and it contains Gata-, Cdx-, Tcf/Lef-, ER71/Etv2- and Fox-binding sites, some of which are bound specifically by each of these transcription factors.	gata	63-67	ets variant 2	Mus musculus	91-95
23271974-5	2012	egl-27 expression is inhibited by daf-2 and activated by pro-longevity factors daf-16/FOXO and elt-3/GATA, suggesting that egl-27 acts at the intersection of IIS and GATA pathways to extend lifespan.	gata	101-105	Egg-laying defective protein 27	Caenorhabditis elegans	0-6
23271974-5	2012	egl-27 expression is inhibited by daf-2 and activated by pro-longevity factors daf-16/FOXO and elt-3/GATA, suggesting that egl-27 acts at the intersection of IIS and GATA pathways to extend lifespan.	gata	101-105	Insulin-like receptor subunit beta;Protein kinase domain-containing protein;Receptor protein-tyrosine kinase	Caenorhabditis elegans	34-39
23271974-5	2012	egl-27 expression is inhibited by daf-2 and activated by pro-longevity factors daf-16/FOXO and elt-3/GATA, suggesting that egl-27 acts at the intersection of IIS and GATA pathways to extend lifespan.	gata	101-105	GATA-type domain-containing protein	Caenorhabditis elegans	95-100
23271974-5	2012	egl-27 expression is inhibited by daf-2 and activated by pro-longevity factors daf-16/FOXO and elt-3/GATA, suggesting that egl-27 acts at the intersection of IIS and GATA pathways to extend lifespan.	gata	101-105	Egg-laying defective protein 27	Caenorhabditis elegans	123-129
23271974-5	2012	egl-27 expression is inhibited by daf-2 and activated by pro-longevity factors daf-16/FOXO and elt-3/GATA, suggesting that egl-27 acts at the intersection of IIS and GATA pathways to extend lifespan.	gata	166-170	Egg-laying defective protein 27	Caenorhabditis elegans	0-6
23271974-5	2012	egl-27 expression is inhibited by daf-2 and activated by pro-longevity factors daf-16/FOXO and elt-3/GATA, suggesting that egl-27 acts at the intersection of IIS and GATA pathways to extend lifespan.	gata	166-170	Insulin-like receptor subunit beta;Protein kinase domain-containing protein;Receptor protein-tyrosine kinase	Caenorhabditis elegans	34-39
23271974-5	2012	egl-27 expression is inhibited by daf-2 and activated by pro-longevity factors daf-16/FOXO and elt-3/GATA, suggesting that egl-27 acts at the intersection of IIS and GATA pathways to extend lifespan.	gata	166-170	Fork-head domain-containing protein;Forkhead box protein O	Caenorhabditis elegans	79-85
23271974-5	2012	egl-27 expression is inhibited by daf-2 and activated by pro-longevity factors daf-16/FOXO and elt-3/GATA, suggesting that egl-27 acts at the intersection of IIS and GATA pathways to extend lifespan.	gata	166-170	GATA-type domain-containing protein	Caenorhabditis elegans	95-100
23271974-5	2012	egl-27 expression is inhibited by daf-2 and activated by pro-longevity factors daf-16/FOXO and elt-3/GATA, suggesting that egl-27 acts at the intersection of IIS and GATA pathways to extend lifespan.	gata	166-170	Egg-laying defective protein 27	Caenorhabditis elegans	123-129
23284307-3	2012	A GATA-1-FOG-1-Mi2 repressor complex was recently demonstrated to be recruited to the -566 GATA motif of the (A)gamma-globin gene.	gata	2-6	zinc finger protein, multitype 1	Mus musculus	9-14
22235304-5	2012	Electrophoretic mobility shift assays and chromatin immunoprecipitation assays showed that GATA-1 directly bound to a GATA binding site in the ZNF268 promoter in vitro and in vivo.	gata	91-95	zinc finger protein 268	Homo sapiens	143-149
22071109-8	2011	As these transcription factors are known to act under the control of the Bmp, Wnt and Fgf families, early Flk1 expression may be induced by cooperative interactions between Gata, Tcf/Lef, Cdx and ER71/Etv2 under the control of Bmp, Wnt and Fgf signaling.	gata	173-177	kinase insert domain protein receptor	Mus musculus	106-110
22194696-2	2011	Intestinal specific transcription is dependent on binding of ELT-2 to GATA binding sites in an iron-dependent enhancer (IDE) located in ftn-1 and ftn-2 promoters, but the mechanism for iron regulation is unknown.	gata	70-74	Transcription factor elt-2	Caenorhabditis elegans	61-66
22194696-2	2011	Intestinal specific transcription is dependent on binding of ELT-2 to GATA binding sites in an iron-dependent enhancer (IDE) located in ftn-1 and ftn-2 promoters, but the mechanism for iron regulation is unknown.	gata	70-74	Ferritin	Caenorhabditis elegans	136-141
22194696-2	2011	Intestinal specific transcription is dependent on binding of ELT-2 to GATA binding sites in an iron-dependent enhancer (IDE) located in ftn-1 and ftn-2 promoters, but the mechanism for iron regulation is unknown.	gata	70-74	Ferritin	Caenorhabditis elegans	146-151
21571865-5	2011	The GATA response was localized to a DNA regulatory region at position -101 in the rat LHbeta gene promoter which overlaps with a previously described cis-element for pituitary homeobox-1 (Pitx1) and is flanked by two SF-1/LRH-1 regulatory sites.	gata	4-8	luteinizing hormone subunit beta	Rattus norvegicus	87-93
21756893-6	2011	Although otx2 can activate both gata5 and gata6, and the prdm1a/krox homologue also activates some endoderm transcription factors, a feedback loop from Gata to otx2 and prdm1a is missing.	gata	152-156	orthodenticle homeobox 2b	Danio rerio	9-13
21756893-6	2011	Although otx2 can activate both gata5 and gata6, and the prdm1a/krox homologue also activates some endoderm transcription factors, a feedback loop from Gata to otx2 and prdm1a is missing.	gata	152-156	GATA binding protein 5	Danio rerio	32-37
21756893-6	2011	Although otx2 can activate both gata5 and gata6, and the prdm1a/krox homologue also activates some endoderm transcription factors, a feedback loop from Gata to otx2 and prdm1a is missing.	gata	152-156	GATA binding protein 6	Danio rerio	42-47
21756893-6	2011	Although otx2 can activate both gata5 and gata6, and the prdm1a/krox homologue also activates some endoderm transcription factors, a feedback loop from Gata to otx2 and prdm1a is missing.	gata	152-156	PR domain containing 1a, with ZNF domain	Danio rerio	57-63
21756893-6	2011	Although otx2 can activate both gata5 and gata6, and the prdm1a/krox homologue also activates some endoderm transcription factors, a feedback loop from Gata to otx2 and prdm1a is missing.	gata	152-156	orthodenticle homeobox 2b	Danio rerio	160-164
21756893-6	2011	Although otx2 can activate both gata5 and gata6, and the prdm1a/krox homologue also activates some endoderm transcription factors, a feedback loop from Gata to otx2 and prdm1a is missing.	gata	152-156	PR domain containing 1a, with ZNF domain	Danio rerio	169-175
21756893-7	2011	Furthermore, we found the positive regulation between gata5 and gata6 to further lock-on the mesendoderm specification by the Gata family.	gata	126-130	GATA binding protein 5	Danio rerio	54-59
21756893-7	2011	Furthermore, we found the positive regulation between gata5 and gata6 to further lock-on the mesendoderm specification by the Gata family.	gata	126-130	GATA binding protein 6	Danio rerio	64-69
21609320-5	2011	We identified a potential GATA-binding site within the human hepcidin promoter.	gata	26-30	hepcidin antimicrobial peptide	Homo sapiens	61-69
21609320-6	2011	Indeed, in hepatic HepG2 cells, luciferase experiments demonstrated that mutation of this GATA-binding site impaired the hepcidin promoter transcriptional activity in basal conditions.	gata	90-94	hepcidin antimicrobial peptide	Homo sapiens	121-129
21609320-10	2011	Finally, we found that mutation of the GATA-binding site impaired the interleukin-6 induction of hepcidin gene expression, but did not prevent the bone morphogenetic protein-6 response.	gata	39-43	interleukin 6	Homo sapiens	70-83
21609320-10	2011	Finally, we found that mutation of the GATA-binding site impaired the interleukin-6 induction of hepcidin gene expression, but did not prevent the bone morphogenetic protein-6 response.	gata	39-43	hepcidin antimicrobial peptide	Homo sapiens	97-105
21571865-5	2011	The GATA response was localized to a DNA regulatory region at position -101 in the rat LHbeta gene promoter which overlaps with a previously described cis-element for pituitary homeobox-1 (Pitx1) and is flanked by two SF-1/LRH-1 regulatory sites.	gata	4-8	paired-like homeodomain 1	Rattus norvegicus	167-187
21571865-5	2011	The GATA response was localized to a DNA regulatory region at position -101 in the rat LHbeta gene promoter which overlaps with a previously described cis-element for pituitary homeobox-1 (Pitx1) and is flanked by two SF-1/LRH-1 regulatory sites.	gata	4-8	paired-like homeodomain 1	Rattus norvegicus	189-194
21571865-5	2011	The GATA response was localized to a DNA regulatory region at position -101 in the rat LHbeta gene promoter which overlaps with a previously described cis-element for pituitary homeobox-1 (Pitx1) and is flanked by two SF-1/LRH-1 regulatory sites.	gata	4-8	splicing factor 1	Rattus norvegicus	218-222
21571865-5	2011	The GATA response was localized to a DNA regulatory region at position -101 in the rat LHbeta gene promoter which overlaps with a previously described cis-element for pituitary homeobox-1 (Pitx1) and is flanked by two SF-1/LRH-1 regulatory sites.	gata	4-8	nuclear receptor subfamily 5, group A, member 2	Rattus norvegicus	223-228
21297973-5	2011	In particular, downregulation of Gata2 expression was mirrored by abundant GATA motifs in regions of reduced histone acetylation suggesting an important role in leukaemogenic transcriptional reprogramming.	gata	75-79	GATA binding protein 2	Mus musculus	33-38
21279818-6	2011	Second, the expression of GATA1 target genes may be modified, at least in part, by GATA2 occupying the GATA-binding motifs.	gata	26-30	GATA binding protein 2	Homo sapiens	83-88
21279818-7	2011	GATA2 is expressed earlier in erythropoiesis than GATA1, and prior GATA2 binding may afford GATA1 access to GATA motifs through epigenetic remodeling and thus facilitate target gene expression.	gata	0-4	GATA binding protein 1	Homo sapiens	92-97
20484821-7	2010	Electrophoretic mobility shift, luciferase reporter, and chromatin immunoprecipitation assays showed that GATA3 binds specifically to a functional double-GATA motif within the GCMB promoter.	gata	106-110	glial cells missing homolog 2	Mus musculus	176-180
21126317-8	2011	By RT-PCR, co-transfection studies and gel-shift assays, we show that Muc5b promoter activity is completely inhibited by TTF-1, whereas factors of the GATA family (GATA-4/GATA-5/GATA-6) are activators.	gata	151-155	GATA binding protein 4	Mus musculus	164-170
20615953-5	2010	The ERV-9 LTR contains multiple CCAAT and GATA motifs and competitively recruits a high concentration of NF-Y and GATA-2 present in low abundance in adult erythroid cells to assemble an LTR/RNA polymerase II complex.	gata	42-46	GATA binding protein 2	Homo sapiens	114-120
20740275-7	2010	The nitrogen source used for growth was suggested to be an important determinant of arsenite toxicity, in keeping with non-enzymatic roles of the URE2 gene product in GATA-type regulation.	gata	167-171	glutathione peroxidase	Saccharomyces cerevisiae S288C	146-150
20346173-4	2010	A typical LMO2 binding site consists of two elements, a GATA site and an E-box, with an interval of 9 approximately 12 bp.	gata	56-60	LIM domain only 2	Homo sapiens	10-14
20384792-8	2010	The results of chromatin immunoprecipitation and electrophoretic mobility shift assays suggested that myogenin bound to GATA4 on the GATA elements and the C-terminal Zn-finger domain of GATA4 and the N-terminal region of myogenin were required for this synergistic activation of transcription.	gata	120-124	myogenin	Rattus norvegicus	102-110
19598245-8	2009	One Point mutation studies revealed that among six potential GATA binding sites located on the upstream region of the bIFNT gene, the one next to ETS2 site exhibited reduced luciferase activity.	gata	61-65	ETS proto-oncogene 2, transcription factor	Bos taurus	146-150
19829305-4	2010	We show that the Fli1 promoter is upregulated by Ets factors Ets1, Ets2, Fli1 and Elf1 either alone or in combination with GATA factors, but is inhibited by Tel.	gata	123-127	Friend leukemia integration 1	Mus musculus	17-21
20402826-7	2010	Here we investigated the way in which Wnt/beta-catenin signalling functionally interacts with the GATA family of pro-cardiogenic transcription factors to regulate subsequent heart muscle differentiation.	gata	98-102	catenin beta 1 L homeolog	Xenopus laevis	42-54
20402826-14	2010	In conclusion, our findings show that the inhibition of heart development by Wnt/beta-catenin signalling during organogenesis is mediated by the loss of expression of GATA pro-cardiogenic transcription factors and reveal functional differences between those GATA factors in heart development.	gata	167-171	catenin beta 1 L homeolog	Xenopus laevis	81-93
20402826-14	2010	In conclusion, our findings show that the inhibition of heart development by Wnt/beta-catenin signalling during organogenesis is mediated by the loss of expression of GATA pro-cardiogenic transcription factors and reveal functional differences between those GATA factors in heart development.	gata	258-262	catenin beta 1 L homeolog	Xenopus laevis	81-93
20523068-3	2010	The double GATA (dblGATA) site is a high-affinity GATA-binding site in the GATA-1 promoter.	gata	11-15	GATA binding protein 1	Mus musculus	75-81
20523068-3	2010	The double GATA (dblGATA) site is a high-affinity GATA-binding site in the GATA-1 promoter.	gata	20-24	GATA binding protein 1	Mus musculus	75-81
19777209-4	2009	The possible role of Ure2p in acquiring sensitivity to oxidative stress by means of its regulatory role in the GATA signal transduction pathway was discussed.	gata	111-115	glutathione peroxidase	Saccharomyces cerevisiae S288C	21-26
19729519-9	2009	One of these enhancers contains functional GATA-binding sites, indicating the potential for a regulatory loop in which GATA factors control the expression of their partner protein FOG-1.	gata	43-47	zinc finger protein, FOG family member 1	Danio rerio	180-185
19729519-9	2009	One of these enhancers contains functional GATA-binding sites, indicating the potential for a regulatory loop in which GATA factors control the expression of their partner protein FOG-1.	gata	119-123	zinc finger protein, FOG family member 1	Danio rerio	180-185
19723625-3	2009	The Gata1 hematopoietic enhancer activity is strictly dependent on a GATA site located in the 5" region of the enhancer.	gata	69-73	GATA binding protein 1	Mus musculus	4-9
19729597-5	2009	p300DeltaC/H3 significantly inhibited p300-induced activation of GATA- and myocyte enhancer factor 2-dependent promoters in cultured ventricular myocytes, and p300DeltaC/H3-TG mice showed cardiac dysfunction that was lethal by 20 weeks of age.	gata	65-69	E1A binding protein p300	Mus musculus	0-4
19700764-5	2009	Chromatin immunoprecipitation (ChIP) analyses revealed that, in TS cells, GATA3 directly regulates Cdx2 transcription from a conserved GATA motif at the intron 1 region of the Cdx2 locus.	gata	74-78	caudal type homeobox 2	Mus musculus	99-103
19306917-8	2009	By transient transfection into Cos-1 and TM4 cells, distal element I which contains GATA-binding sites and proximal element B containing the sex-determining region on Y chromosome gene (SRY) binding site were revealed to have an important role in transcriptional regulation of the wrasse DMRT1 when an enhancer sequence was provided.	gata	84-88	doublesex and mab-3 related transcription factor 1	Mus musculus	288-293
19700764-5	2009	Chromatin immunoprecipitation (ChIP) analyses revealed that, in TS cells, GATA3 directly regulates Cdx2 transcription from a conserved GATA motif at the intron 1 region of the Cdx2 locus.	gata	74-78	caudal type homeobox 2	Mus musculus	176-180
19497978-10	2009	Moreover, the activity of MED1 for SULT2A1 promoter was mediated by GATA-6 via the -190 GATA-binding site.	gata	68-72	mediator complex subunit 1	Homo sapiens	26-30
19497978-10	2009	Moreover, the activity of MED1 for SULT2A1 promoter was mediated by GATA-6 via the -190 GATA-binding site.	gata	68-72	sulfotransferase family 2A member 1	Homo sapiens	35-42
19357811-5	2009	Moreover, the promoter activity of 2487 eLuc containing two novel GATA sites was significantly elevated by co-transfection of a GATA-2 expression vector in proliferating Rcho-1 cells.	gata	66-70	GATA binding protein 2	Rattus norvegicus	128-134
19104072-4	2009	In this article, we demonstrate that the extent to which Sit4 plays a role in NCR-sensitive transcription depends upon whether or not (i) Gzf3, a GATA repressor homologous to Dal80, is active in the genetic background assayed; (ii) Gat1 is able to activate transcription of the assayed gene in the absence of Gln3 in that genetic background; and (iii) the gene chosen as a reporter is able to be transcribed by Gln3 or Gat1 in the absence of the other GATA factor.	gata	146-150	type 2A-related serine/threonine-protein phosphatase SIT4	Saccharomyces cerevisiae S288C	57-61
19104072-4	2009	In this article, we demonstrate that the extent to which Sit4 plays a role in NCR-sensitive transcription depends upon whether or not (i) Gzf3, a GATA repressor homologous to Dal80, is active in the genetic background assayed; (ii) Gat1 is able to activate transcription of the assayed gene in the absence of Gln3 in that genetic background; and (iii) the gene chosen as a reporter is able to be transcribed by Gln3 or Gat1 in the absence of the other GATA factor.	gata	452-456	type 2A-related serine/threonine-protein phosphatase SIT4	Saccharomyces cerevisiae S288C	57-61
19355882-10	2009	Furthermore, preclinical respectively clinical trials have been performed with small orally active drugs that stimulate endogenous EPO production by activating the EPO promoter ("GATA-inhibitors": diazepane derivatives) or enhancer ("HIF-stabilizers": 2-oxoglutarate analogues).	gata	179-183	erythropoietin	Homo sapiens	131-134
18845640-6	2009	In placental trophoblast giant cells, cAMP is required for activation of the Star promoter, and the cis-elements mediating a maximal response were defined as cAMP response element 2 and GATA.	gata	186-190	steroidogenic acute regulatory protein	Rattus norvegicus	77-81
19095651-3	2009	Unlike other GATA-type zinc fingers that recognize the consensus sequence (A/C/T)GATA(A/G), the MED-1 zinc finger (MED1zf) binds the larger and atypical site GTATACT(T/C)(3).	gata	13-17	mediator complex subunit 1	Homo sapiens	96-101
19355882-10	2009	Furthermore, preclinical respectively clinical trials have been performed with small orally active drugs that stimulate endogenous EPO production by activating the EPO promoter ("GATA-inhibitors": diazepane derivatives) or enhancer ("HIF-stabilizers": 2-oxoglutarate analogues).	gata	179-183	erythropoietin	Homo sapiens	164-167
18003741-0	2007	Notch-GATA synergy promotes endoderm-specific expression of ref-1 in C. elegans.	gata	6-10	REgulator of Fusion	Caenorhabditis elegans	60-65
18951515-0	2008	Requirement of TCTG(G/C) Direct Repeats and Overlapping GATA Site for Maintaining the Cardiac-Specific Expression of Cardiac troponin T in Developing and Adult Mice.	gata	56-60	troponin T2, cardiac type	Rattus norvegicus	117-135
18591257-7	2008	We show that GATA4 is required for cyclin D2, cyclin A2, and Cdk4 expression in the right ventricle and that the Cyclin D2 and Cdk4 promoters are bound and activated by GATA4 via multiple consensus GATA binding sites in each gene"s proximal promoter.	gata	13-17	cyclin D2	Mus musculus	35-44
18591257-7	2008	We show that GATA4 is required for cyclin D2, cyclin A2, and Cdk4 expression in the right ventricle and that the Cyclin D2 and Cdk4 promoters are bound and activated by GATA4 via multiple consensus GATA binding sites in each gene"s proximal promoter.	gata	13-17	cyclin A2	Mus musculus	46-55
18591257-7	2008	We show that GATA4 is required for cyclin D2, cyclin A2, and Cdk4 expression in the right ventricle and that the Cyclin D2 and Cdk4 promoters are bound and activated by GATA4 via multiple consensus GATA binding sites in each gene"s proximal promoter.	gata	13-17	cyclin-dependent kinase 4	Mus musculus	61-65
18591257-7	2008	We show that GATA4 is required for cyclin D2, cyclin A2, and Cdk4 expression in the right ventricle and that the Cyclin D2 and Cdk4 promoters are bound and activated by GATA4 via multiple consensus GATA binding sites in each gene"s proximal promoter.	gata	13-17	cyclin D2	Mus musculus	113-122
18591257-7	2008	We show that GATA4 is required for cyclin D2, cyclin A2, and Cdk4 expression in the right ventricle and that the Cyclin D2 and Cdk4 promoters are bound and activated by GATA4 via multiple consensus GATA binding sites in each gene"s proximal promoter.	gata	13-17	GATA binding protein 4	Mus musculus	169-174
18522800-5	2008	In 3T3-L1 preadipocytes, the transcriptional factors GATA-2 and GATA-3 are known to down-regulate adipogenesis by direct binding to the C/EBPbeta protein and to the GATA-binding site on the PPARgamma2 promoter.	gata	53-57	GATA binding protein 3	Mus musculus	64-70
18522800-5	2008	In 3T3-L1 preadipocytes, the transcriptional factors GATA-2 and GATA-3 are known to down-regulate adipogenesis by direct binding to the C/EBPbeta protein and to the GATA-binding site on the PPARgamma2 promoter.	gata	53-57	CCAAT/enhancer binding protein (C/EBP), beta	Mus musculus	136-145
18522800-5	2008	In 3T3-L1 preadipocytes, the transcriptional factors GATA-2 and GATA-3 are known to down-regulate adipogenesis by direct binding to the C/EBPbeta protein and to the GATA-binding site on the PPARgamma2 promoter.	gata	53-57	peroxisome proliferator activated receptor gamma	Mus musculus	190-200
18448117-7	2008	We showed that ELT-2 and PHA-4 proteins interact directly with the GATA and forkhead binding sequences, respectively, in gel mobility shift assays.	gata	67-71	Transcription factor elt-2	Caenorhabditis elegans	15-20
18448117-7	2008	We showed that ELT-2 and PHA-4 proteins interact directly with the GATA and forkhead binding sequences, respectively, in gel mobility shift assays.	gata	67-71	Defective pharyngeal development protein 4	Caenorhabditis elegans	25-30
18174356-5	2008	Insights into the functional roles played by GATA factors in adult organ systems have been hampered by the early embryonic lethality associated with the different Gata-null mice.	gata	163-167	glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1	Mus musculus	45-49
18024960-6	2008	Site-directed mutagenesis of the GATA sequences, singly or in combination, reduces ftn-1 GFP reporter expression in the intestine.	gata	33-37	Ferritin	Caenorhabditis elegans	83-88
18024960-7	2008	In vitro DNA mobility shift assays show that the intestine-specific GATA protein ELT-2 binds to both GATA sequences.	gata	68-72	Transcription factor elt-2	Caenorhabditis elegans	81-86
18671946-5	2008	Sm up-regulated the binding activity of GATA-6 to SM-MHC GATA site and activated the transfected SM-MHC promoter in proliferative VSMCs, while mutating the GATA-6 binding site abolished this activation.	gata	40-44	myosin heavy chain 11	Homo sapiens	50-56
18625887-8	2008	ETO2-dependent direct repression of the Pf4 proximal promoter is mediated by GATA-binding sites and an E-Box motif.	gata	77-81	CBFA2/RUNX1 partner transcriptional co-repressor 3	Homo sapiens	0-4
18625887-8	2008	ETO2-dependent direct repression of the Pf4 proximal promoter is mediated by GATA-binding sites and an E-Box motif.	gata	77-81	platelet factor 4	Homo sapiens	40-43
18443038-4	2008	DNA-protein binding assays showed that the GATA motif of interest is capable of binding GATA-1 transcription factor in vitro and in vivo.	gata	43-47	GATA binding protein 1	Homo sapiens	88-94
18347053-0	2008	Silencing of Agamma-globin gene expression during adult definitive erythropoiesis mediated by GATA-1-FOG-1-Mi2 complex binding at the -566 GATA site.	gata	94-98	zinc finger protein, multitype 1	Mus musculus	101-106
17687519-13	2007	Chromatin immunoprecipitation revealed that GATA, AP-1 and NF-AT binding to IL-5 promoter was induced by LPS stimulation and that TQ inhibited GATA binding at the IL-5 promoter but did not affect AP-1 and NF-AT binding.	gata	44-48	interleukin 5	Rattus norvegicus	76-80
17728253-11	2007	GATA enhancer sequences govern DKF-2 expression in intestine in vivo.	gata	0-4	Serine/threonine-protein kinase dkf-2	Caenorhabditis elegans	31-36
17555758-2	2007	The cytokine IL-5 and a high-affinity double GATA-binding site within the GATA-1 promoter are critical for eosinophilopoiesis.	gata	45-49	GATA binding protein 1	Mus musculus	74-80
17909262-6	2007	The Cyp19 promoter contains a cAMP response element-like sequence (CLS), two nuclear receptor elements half sites (NREs), a GATA binding site, a Yin Yang-1 (YY1) response element, and an activation protein 3 (AP3) binding site.	gata	124-128	cytochrome P450, family 19, subfamily a, polypeptide 1	Rattus norvegicus	4-9
17909262-12	2007	Our results indicate that CLS is active only in follicles; whereas in the CL, binding to the GATA, NRE, and AP3 sites associates with changes in Cyp19 expression, suggesting that they control Cyp19 promoter activity in luteal cells.	gata	93-97	cardiolipin synthase 1	Rattus norvegicus	26-29
17909262-12	2007	Our results indicate that CLS is active only in follicles; whereas in the CL, binding to the GATA, NRE, and AP3 sites associates with changes in Cyp19 expression, suggesting that they control Cyp19 promoter activity in luteal cells.	gata	93-97	cytochrome P450, family 19, subfamily a, polypeptide 1	Rattus norvegicus	145-150
17875210-0	2007	GATA elements control repression of cardiac troponin I promoter activity in skeletal muscle cells.	gata	0-4	troponin I, cardiac 3	Mus musculus	36-54
17875210-1	2007	BACKGROUND: We reported previously that the cardiac troponin I (cTnI) promoter drives cardiac-specific expression of reporter genes in cardiac muscle cells and in transgenic mice, and that disruption of GATA elements inactivates the cTnI promoter in cultured cardiomyocytes.	gata	203-207	troponin I, cardiac 3	Mus musculus	44-62
17875210-1	2007	BACKGROUND: We reported previously that the cardiac troponin I (cTnI) promoter drives cardiac-specific expression of reporter genes in cardiac muscle cells and in transgenic mice, and that disruption of GATA elements inactivates the cTnI promoter in cultured cardiomyocytes.	gata	203-207	troponin I, cardiac 3	Mus musculus	64-68
17875210-1	2007	BACKGROUND: We reported previously that the cardiac troponin I (cTnI) promoter drives cardiac-specific expression of reporter genes in cardiac muscle cells and in transgenic mice, and that disruption of GATA elements inactivates the cTnI promoter in cultured cardiomyocytes.	gata	203-207	troponin I, cardiac 3	Mus musculus	233-237
17875210-3	2007	RESULTS: Mutation or deletion of GATA elements induces a strong transcriptional activation of the cTnI promoter in regenerating skeletal muscle and in cultured skeletal muscle cells.	gata	33-37	troponin I, cardiac 3	Mus musculus	98-102
17875210-4	2007	Electrophoretic mobility shift assays show that proteins present in nuclear extracts of C2C12 muscle cells bind the GATA motifs present in the cTnI promoter.	gata	116-120	troponin I, cardiac 3	Mus musculus	143-147
17592720-3	2007	Isolation and functional analysis of the Fet3 promoter indicate that a GATA sequence element plays a role in iron-dependent expression of Fet3.	gata	71-75	ferroxidase FET3	Saccharomyces cerevisiae S288C	41-45
17592720-3	2007	Isolation and functional analysis of the Fet3 promoter indicate that a GATA sequence element plays a role in iron-dependent expression of Fet3.	gata	71-75	ferroxidase FET3	Saccharomyces cerevisiae S288C	138-142
17611647-10	2007	Two GATA-binding sites within intron 6 of human JMJD2B gene were conserved in mouse Jmjd2b gene.	gata	4-8	lysine demethylase 4B	Homo sapiens	48-54
17611647-10	2007	Two GATA-binding sites within intron 6 of human JMJD2B gene were conserved in mouse Jmjd2b gene.	gata	4-8	lysine (K)-specific demethylase 4B	Mus musculus	84-90
17587490-5	2007	Our results indicate that GATA binding sites at -90 and -81 in the rat BNP promoter are essential for the in vivo response to Ang II.	gata	26-30	natriuretic peptide B	Rattus norvegicus	71-74
17587490-5	2007	Our results indicate that GATA binding sites at -90 and -81 in the rat BNP promoter are essential for the in vivo response to Ang II.	gata	26-30	angiotensinogen	Rattus norvegicus	126-132
17605826-6	2007	Although the in vivo contribution is limited to cells of parietal endoderm lineage, Gata-induced extra-embryonic endoderm cells (gExEn) can be induced to differentiate into visceral endoderm-like cells in vitro by repression of Gata6.	gata	84-88	GATA binding protein 6	Mus musculus	228-233
17290010-7	2007	-40 and -89 GATA binding sites in the IFABP promoter were required for the synergistic activation by Smad2, 3, and 4 and GATA4.	gata	12-16	fatty acid binding protein 2	Homo sapiens	38-43
17290010-7	2007	-40 and -89 GATA binding sites in the IFABP promoter were required for the synergistic activation by Smad2, 3, and 4 and GATA4.	gata	12-16	SMAD family member 2	Homo sapiens	101-109
17290010-7	2007	-40 and -89 GATA binding sites in the IFABP promoter were required for the synergistic activation by Smad2, 3, and 4 and GATA4.	gata	12-16	GATA binding protein 4	Homo sapiens	121-126
17227882-5	2007	Mutation of the GATA binding site on the Cyp19 promoter and inhibition of GATA4 expression with specific small interfering RNA significantly reduced FSH-enhanced Cyp19 expression, whereas overexpression of GATA4 increased Cyp19 promoter activity.	gata	16-20	cytochrome P450, family 19, subfamily a, polypeptide 1	Rattus norvegicus	41-46
17437998-5	2007	In addition, SSBP2 was found to augment transcription of the Protein 4.2 (P4.2) gene, a direct target of the E-box-GATA-binding complex, in an Ldb1-dependent manner and to increase endogenous Ldb1 and Lmo2 protein levels, E-box-GATA DNA-binding activity, and P4.2 and beta-globin expression in erythroid progenitors.	gata	115-119	single stranded DNA binding protein 2	Homo sapiens	13-18
17437998-5	2007	In addition, SSBP2 was found to augment transcription of the Protein 4.2 (P4.2) gene, a direct target of the E-box-GATA-binding complex, in an Ldb1-dependent manner and to increase endogenous Ldb1 and Lmo2 protein levels, E-box-GATA DNA-binding activity, and P4.2 and beta-globin expression in erythroid progenitors.	gata	115-119	erythrocyte membrane protein band 4.2	Homo sapiens	61-72
17437998-5	2007	In addition, SSBP2 was found to augment transcription of the Protein 4.2 (P4.2) gene, a direct target of the E-box-GATA-binding complex, in an Ldb1-dependent manner and to increase endogenous Ldb1 and Lmo2 protein levels, E-box-GATA DNA-binding activity, and P4.2 and beta-globin expression in erythroid progenitors.	gata	115-119	erythrocyte membrane protein band 4.2	Homo sapiens	74-78
17437998-5	2007	In addition, SSBP2 was found to augment transcription of the Protein 4.2 (P4.2) gene, a direct target of the E-box-GATA-binding complex, in an Ldb1-dependent manner and to increase endogenous Ldb1 and Lmo2 protein levels, E-box-GATA DNA-binding activity, and P4.2 and beta-globin expression in erythroid progenitors.	gata	228-232	single stranded DNA binding protein 2	Homo sapiens	13-18
17437998-5	2007	In addition, SSBP2 was found to augment transcription of the Protein 4.2 (P4.2) gene, a direct target of the E-box-GATA-binding complex, in an Ldb1-dependent manner and to increase endogenous Ldb1 and Lmo2 protein levels, E-box-GATA DNA-binding activity, and P4.2 and beta-globin expression in erythroid progenitors.	gata	228-232	erythrocyte membrane protein band 4.2	Homo sapiens	61-72
17437998-5	2007	In addition, SSBP2 was found to augment transcription of the Protein 4.2 (P4.2) gene, a direct target of the E-box-GATA-binding complex, in an Ldb1-dependent manner and to increase endogenous Ldb1 and Lmo2 protein levels, E-box-GATA DNA-binding activity, and P4.2 and beta-globin expression in erythroid progenitors.	gata	228-232	erythrocyte membrane protein band 4.2	Homo sapiens	74-78
17242194-7	2007	Transient transfections in human primary endothelial cells derived from umbilical vein (HUVECs) demonstrated that VE-cadherin promoter activity was dependent on the integrity of a specialized E-box associated with a GATA motif and was maximal with the coexpression of the different components of the TAL-1 complex.	gata	216-220	cadherin 5	Homo sapiens	114-125
17227882-5	2007	Mutation of the GATA binding site on the Cyp19 promoter and inhibition of GATA4 expression with specific small interfering RNA significantly reduced FSH-enhanced Cyp19 expression, whereas overexpression of GATA4 increased Cyp19 promoter activity.	gata	16-20	cytochrome P450, family 19, subfamily a, polypeptide 1	Rattus norvegicus	162-167
17227882-5	2007	Mutation of the GATA binding site on the Cyp19 promoter and inhibition of GATA4 expression with specific small interfering RNA significantly reduced FSH-enhanced Cyp19 expression, whereas overexpression of GATA4 increased Cyp19 promoter activity.	gata	16-20	cytochrome P450, family 19, subfamily a, polypeptide 1	Rattus norvegicus	162-167
17312153-7	2007	This suppression of the TGF-beta1 promoter is mediated by the -1079 to -406 region, in which deletion of a GATA-binding motif at position -821 abrogates NF-AT-mediated activation of the TGF-beta1 promoter.	gata	107-111	transforming growth factor, beta 1	Mus musculus	24-33
17312153-7	2007	This suppression of the TGF-beta1 promoter is mediated by the -1079 to -406 region, in which deletion of a GATA-binding motif at position -821 abrogates NF-AT-mediated activation of the TGF-beta1 promoter.	gata	107-111	transforming growth factor, beta 1	Mus musculus	186-195
16924465-4	2006	Stimulation of cardiomyocytes with 100 nM AngII for 2 h activated the transcription factors AP-1 and GATA by 68.6+/-23.9 or 70.7+/-9.8%.	gata	101-105	angiotensinogen	Rattus norvegicus	42-47
16979593-3	2006	EMSA with DNA probes within the region reveals that binding of GATA motif bound proteins was decreased by LPS-treatment.	gata	63-67	toll-like receptor 4	Mus musculus	106-109
17113066-8	2007	There are three zinc-finger GATA-type factors that are candidates to bind this extended GATA site in the differentiating C. elegans intestine: ELT-2, ELT-4 and ELT-7.	gata	28-32	Transcription factor elt-2	Caenorhabditis elegans	143-148
17113066-8	2007	There are three zinc-finger GATA-type factors that are candidates to bind this extended GATA site in the differentiating C. elegans intestine: ELT-2, ELT-4 and ELT-7.	gata	28-32	GATA-type domain-containing protein	Caenorhabditis elegans	150-155
17113066-8	2007	There are three zinc-finger GATA-type factors that are candidates to bind this extended GATA site in the differentiating C. elegans intestine: ELT-2, ELT-4 and ELT-7.	gata	28-32	Transcription factor elt-7	Caenorhabditis elegans	160-165
16924465-9	2006	In contrast to the early induction of GATA and AP-1, the transcription factor similar to mothers against decapentaplegic homolog (SMAD) was induced by AngII after 24 h. This stimulation was dependent on TGF-beta1 because it was blocked by antibodies specific for TGF-beta1.	gata	38-42	angiotensinogen	Rattus norvegicus	151-156
16924465-9	2006	In contrast to the early induction of GATA and AP-1, the transcription factor similar to mothers against decapentaplegic homolog (SMAD) was induced by AngII after 24 h. This stimulation was dependent on TGF-beta1 because it was blocked by antibodies specific for TGF-beta1.	gata	38-42	transforming growth factor, beta 1	Rattus norvegicus	203-212
16407417-11	2006	The proximal smMLCK promoter also contains a consensus GATA-binding site that bound GATA-6.	gata	55-59	myosin, light polypeptide kinase	Mus musculus	13-19
16762033-3	2006	The HvMYBS3 protein expressed in bacteria binds to oligonucleotides containing a GATA core derived from the promoters of: (i) the developing endosperm gene Itr1 (5"-GATAAGATA-3") encoding trypsin inhibitor BTI-CMe, and (ii) the post-germinating aleurone gene Amy6.4 (5"-TATCCAC-3"/5"-GTGGATA-3") encoding a high-pI alpha-amylase.	gata	81-85	ITR1	Hordeum vulgare	156-160
16949798-6	2006	Expression of a dominant-interfering form of GATA6, which inhibits transactivation of GATA targets, severely impairs the ability of dorsal leading edge mesendoderm to spread and translocate on fibronectin.	gata	45-49	fibronectin 1 S homeolog	Xenopus laevis	193-204
16407417-11	2006	The proximal smMLCK promoter also contains a consensus GATA-binding site that bound GATA-6.	gata	55-59	GATA binding protein 6	Mus musculus	84-90
16452489-7	2006	Here we report that GATA-4, a transcription factor essential for heart development, binds to the Grp78 promoter in vivo and activates the ERSE, which does not contain a consensus GATA binding site.	gata	20-24	heat shock protein 5	Mus musculus	97-102
16720723-7	2006	Transient transfection experiments in KK-1 cells demonstrated that dominant negative GATA-4 variants or mutations of GATA-binding sites in the inhibin-alpha promoter attenuated TGF-beta-induced gene activation.	gata	85-89	transforming growth factor, beta 1	Mus musculus	177-185
16437149-0	2006	The GATA site-dependent hemogen promoter is transcriptionally regulated by GATA1 in hematopoietic and leukemia cells.	gata	4-8	GATA binding protein 1	Homo sapiens	75-80
16437149-4	2006	GATA1, not GATA2, binds to the GATA binding sites and transactivates the Hemgn promoter in a dose-dependent manner.	gata	0-4	hemogen	Homo sapiens	73-78
16325171-3	2006	We have previously shown that the binding site recognized by MED-1 is a noncanonical RAGTATAC site that is not expected from the resemblance of its single C4-type zinc finger to those of other known GATA factors, which recognize the consensus HGATAR.	gata	199-203	GATA-type domain-containing protein	Caenorhabditis elegans	61-66
16373364-2	2006	An important role for the proximal AP-1 and GATA sites in regulating IL-5 transcription is generally accepted but the significance of an adjacent Ets/NFAT site has remained unclear.	gata	44-48	interleukin 5	Mus musculus	69-73
16373364-6	2006	Mutagenesis showed that the Ets/NFAT site is of critical importance along with the AP-1 and GATA sites in regulating IL-5 transcription stimulated by PMA/cAMP and MAP kinase activation.	gata	92-96	interleukin 5	Mus musculus	117-121
16055713-0	2005	GATA motifs regulate early hematopoietic lineage-specific expression of the Gata2 gene.	gata	0-4	GATA binding protein 2	Mus musculus	76-81
16413408-6	2006	The ability of mouse GATA factors to transactivate the Nox1 promoter was demonstrated in Cos-7 cells and site-directed mutagenesis of the conserved GATA-binding site further demonstrates that the regulation of Nox1 transcription is mediated by the direct binding of a GATA factor to the Nox1 proximal promoter.	gata	21-25	NADPH oxidase 1	Mus musculus	55-59
16413408-6	2006	The ability of mouse GATA factors to transactivate the Nox1 promoter was demonstrated in Cos-7 cells and site-directed mutagenesis of the conserved GATA-binding site further demonstrates that the regulation of Nox1 transcription is mediated by the direct binding of a GATA factor to the Nox1 proximal promoter.	gata	21-25	NADPH oxidase 1	Homo sapiens	210-214
16413408-6	2006	The ability of mouse GATA factors to transactivate the Nox1 promoter was demonstrated in Cos-7 cells and site-directed mutagenesis of the conserved GATA-binding site further demonstrates that the regulation of Nox1 transcription is mediated by the direct binding of a GATA factor to the Nox1 proximal promoter.	gata	21-25	NADPH oxidase 1	Homo sapiens	210-214
16286657-4	2005	We found that conditionally active GATA-1 (ER-GATA-1) and GATA-2 occupy only a small subset of the conserved GATA motifs within the murine beta-globin locus.	gata	35-39	GATA binding protein 1	Mus musculus	43-52
16286657-5	2005	Kinetic analyses in GATA-1-null cells indicated that ER-GATA-1 preferentially occupied GATA motifs at the locus control region (LCR), in which chromatin accessibility is largely GATA-1-independent.	gata	20-24	GATA binding protein 1	Mus musculus	53-62
16286657-5	2005	Kinetic analyses in GATA-1-null cells indicated that ER-GATA-1 preferentially occupied GATA motifs at the locus control region (LCR), in which chromatin accessibility is largely GATA-1-independent.	gata	20-24	GATA binding protein 1	Mus musculus	56-62
16274253-11	2005	Deletion of either the 5" E box or the 3" E box and the GATA element in the VEGFR-2 promoter completely abolished the inhibition of VEGFR-2 promoter activity elicited by VEGFR-1 siRNA.	gata	56-60	kinase insert domain receptor	Bos taurus	76-83
16274253-11	2005	Deletion of either the 5" E box or the 3" E box and the GATA element in the VEGFR-2 promoter completely abolished the inhibition of VEGFR-2 promoter activity elicited by VEGFR-1 siRNA.	gata	56-60	kinase insert domain receptor	Bos taurus	132-139
16274253-11	2005	Deletion of either the 5" E box or the 3" E box and the GATA element in the VEGFR-2 promoter completely abolished the inhibition of VEGFR-2 promoter activity elicited by VEGFR-1 siRNA.	gata	56-60	fms related receptor tyrosine kinase 1	Bos taurus	170-177
15980430-9	2005	In addition, PKN increased the activities of serum-response factor (SRF), GATA, and MEF2-dependent enhancer-reporters.	gata	74-78	protein kinase N1	Homo sapiens	13-16
16012775-10	2005	GATA and E47 binding sites were conserved among human FGF23, rat Fgf23, and mouse Fgf23 promoters.	gata	0-4	fibroblast growth factor 23	Homo sapiens	54-59
16012775-10	2005	GATA and E47 binding sites were conserved among human FGF23, rat Fgf23, and mouse Fgf23 promoters.	gata	0-4	fibroblast growth factor 23	Rattus norvegicus	65-70
16012775-10	2005	GATA and E47 binding sites were conserved among human FGF23, rat Fgf23, and mouse Fgf23 promoters.	gata	0-4	fibroblast growth factor 23	Mus musculus	82-87
15869801-2	2005	In sheep, we recently discovered a putative GATA-binding site (WGATAR) in the second intron of the Th1-cytokine gene interleukin 2 (IL2), showing a single nucleotide polymorphism (G/C).	gata	44-48	interleukin-2	Ovis aries	117-130
15869801-2	2005	In sheep, we recently discovered a putative GATA-binding site (WGATAR) in the second intron of the Th1-cytokine gene interleukin 2 (IL2), showing a single nucleotide polymorphism (G/C).	gata	44-48	interleukin-2	Ovis aries	132-135
16055713-5	2005	Detailed transgenic mouse reporter expression analyses demonstrate that five GATA motifs within the 3.1-kbp Gata2 early hematopoietic regulatory domain (G2-EHRD) were essential for GFP expression within the dorsal aortic wall, where hemangioblasts, the earliest precursors possessing both hematopoietic and vascular developmental potential, are thought to reside.	gata	77-81	GATA binding protein 2	Mus musculus	108-113
12888492-4	2003	We found that str1+ is subject to negative transcriptional regulation, which is exerted through binding of Fep1 to a single GATA element in the str1+ promoter.	gata	124-128	cystathionine gamma-lyase CYS3	Saccharomyces cerevisiae S288C	14-18
15843409-6	2005	The Mef2c AHF enhancer relies on Isl1- and Gata-binding sites.	gata	43-47	myocyte enhancer factor 2C	Mus musculus	4-9
15780659-2	2005	One such system, the target of rapamycin (Tor) proteins, senses nutrients and uses the GATA activators Gln3p and Nil1p to regulate translation in response to low-quality carbon and nitrogen.	gata	87-91	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	103-108
15780659-2	2005	One such system, the target of rapamycin (Tor) proteins, senses nutrients and uses the GATA activators Gln3p and Nil1p to regulate translation in response to low-quality carbon and nitrogen.	gata	87-91	Gat1p	Saccharomyces cerevisiae S288C	113-118
15737937-4	2005	We report that MED-1 binds invariant noncanonical sites in the end genes, revealing that the MEDs are atypical members of the GATA factor family that do not recognize GATA sequences.	gata	126-130	GATA-type domain-containing protein	Caenorhabditis elegans	15-20
15539431-6	2005	Mutation of the GATA binding site on G5 abrogated the transcriptional activation mediated by Gata-4 and reduced basal glucagon gene promoter activity in glucagon-producing cells by 55%.	gata	16-20	LOW QUALITY PROTEIN: transcription factor GATA-4	Cricetulus griseus	93-99
15670213-2	2005	GATA-binding motifs have been found in the regulatory regions of various erythroid-specific genes, suggesting that GATA-1 contributes to gene regulation during the entire process of erythropoiesis.	gata	0-4	GATA binding protein 1	Mus musculus	115-121
15541382-3	2004	Having found putative GATA binding sites in the murine Muc2 promoter and that GATA-4 is expressed in Muc2-expressing goblet cells of the mouse small intestine, we undertook to study its regulation by this transcription factor.	gata	22-26	mucin 2	Mus musculus	55-59
15501582-8	2004	In all postnatal ovaries, the expression of P450scc localized with tissue expressing GATA-4 and/or GATA-6, but GATA expression also occurred in P450scc negative cells.	gata	85-89	cytochrome P450, family 11, subfamily a, polypeptide 1	Rattus norvegicus	44-51
15896659-2	2005	We identified and characterized a new C/T substitution at position -689 (-689C>T) in the P2 promoter of PPARgamma in a putative GATA binding site.	gata	131-135	peroxisome proliferator activated receptor gamma	Homo sapiens	107-116
15862566-10	2005	The zebrafish ff1a dual promoter contains several GATA binding sites and E-boxes, a site for DR4, XFD2, MyoD, Snail, HNF3, S8, and an HMG-box recognition site for Sox9.	gata	50-54	nuclear receptor subfamily 5, group A, member 2	Danio rerio	14-18
15659482-8	2005	Together with the timing of their expression and the effects of GATA MOs in vivo, these observations identify GATA6 as the predominant GATA factor in the maintenance of endodermal gene expression by TGFbeta signaling in gastrulating embryos.	gata	64-68	GATA binding protein 6 L homeolog	Xenopus laevis	110-115
15572669-3	2004	For example, prohypertrophic transcription factors belonging to the nuclear factor of activated T cells (NFAT) and GATA families are subject to CRM1-dependent nuclear export but are rapidly relocalized to the nucleus in response to cues for hypertrophic growth.	gata	115-119	exportin 1	Homo sapiens	144-148
15256532-4	2004	A GATA-4 expression plasmid cotransfected with a murine LHR promoter-driven luciferase reporter plasmid, containing a consensus GATA-binding site, induced a dose-dependent significant transactivation of the LHR promoter in nonsteroidogenic human embryonic kidney 293, steroidogenic murine mLTC-1 Leydig cells and in murine adrenal Y-1 cells.	gata	2-6	luteinizing hormone/choriogonadotropin receptor	Mus musculus	56-59
15256532-4	2004	A GATA-4 expression plasmid cotransfected with a murine LHR promoter-driven luciferase reporter plasmid, containing a consensus GATA-binding site, induced a dose-dependent significant transactivation of the LHR promoter in nonsteroidogenic human embryonic kidney 293, steroidogenic murine mLTC-1 Leydig cells and in murine adrenal Y-1 cells.	gata	2-6	luteinizing hormone/choriogonadotropin receptor	Mus musculus	207-210
15302915-7	2004	Transfections with wild-type and mutant promoter constructs in cardiac HL-1 cells indicated that one GATA box is absolutely required for high alphaT-catenin promoter activity in these cells.	gata	101-105	catenin (cadherin associated protein), alpha 3	Mus musculus	142-156
15123623-7	2004	An estrogen receptor fusion to GATA-1 (ER-GATA-1) and endogenous GATA-1 both occupied a region of Tac-2 intron-7, which contains two conserved GATA motifs.	gata	31-35	GATA binding protein 1	Mus musculus	39-48
15123623-7	2004	An estrogen receptor fusion to GATA-1 (ER-GATA-1) and endogenous GATA-1 both occupied a region of Tac-2 intron-7, which contains two conserved GATA motifs.	gata	31-35	GATA binding protein 1	Mus musculus	42-48
15123623-7	2004	An estrogen receptor fusion to GATA-1 (ER-GATA-1) and endogenous GATA-1 both occupied a region of Tac-2 intron-7, which contains two conserved GATA motifs.	gata	31-35	tachykinin 2	Mus musculus	98-103
15140029-10	2004	In conclusion, we have identified a novel polymorphic GATA site that may affect transciptional activity of the human IL-12Rbeta2 gene under GATA3-mediated, Th2-polarizing conditions.	gata	54-58	GATA binding protein 3	Homo sapiens	140-145
14701820-5	2004	HS1 participates in the transcriptional autoregulation of GATA-1 through an essential GATA-binding site that is footprinted in vivo.	gata	58-62	eukaryotic translation elongation factor 1 alpha 2	Homo sapiens	0-3
14555463-6	2004	In response to TNF-alpha treatment for 4 h, nuclear protein binding to (32)P oligonucleotides was characterized as: 1) a significant increase in binding to (-370)CACCC, 2) a significant decrease in binding to (-231)GATA, and 3) no change in (-186)CACCC binding.	gata	215-219	tumor necrosis factor	Homo sapiens	15-24
14614148-0	2003	Endothelial lineage-mediated loss of the GATA cofactor Friend of GATA 1 impairs cardiac development.	gata	41-45	zinc finger protein, multitype 1	Mus musculus	55-71
14613857-9	2003	Furthermore, the coregulator of GATA, FOG2, markedly suppresses the GATA-induced increase in myocytes, but enhances it in PC12 cells.	gata	32-36	zinc finger protein, multitype 2	Rattus norvegicus	38-42
14613857-9	2003	Furthermore, the coregulator of GATA, FOG2, markedly suppresses the GATA-induced increase in myocytes, but enhances it in PC12 cells.	gata	68-72	zinc finger protein, multitype 2	Rattus norvegicus	38-42
14613857-10	2003	The use of GATA mutants that are incapable of forming complexes with FOG2 indicates that the formation of GATA-FOG complexes is required for the FOG2-induced suppression in myocytes, but not for the FOG2-mediated enhancement in PC12 cells.	gata	106-110	zinc finger protein, multitype 2	Rattus norvegicus	69-73
14613857-10	2003	The use of GATA mutants that are incapable of forming complexes with FOG2 indicates that the formation of GATA-FOG complexes is required for the FOG2-induced suppression in myocytes, but not for the FOG2-mediated enhancement in PC12 cells.	gata	106-110	zinc finger protein, multitype 2	Rattus norvegicus	145-149
14613857-10	2003	The use of GATA mutants that are incapable of forming complexes with FOG2 indicates that the formation of GATA-FOG complexes is required for the FOG2-induced suppression in myocytes, but not for the FOG2-mediated enhancement in PC12 cells.	gata	106-110	zinc finger protein, multitype 2	Rattus norvegicus	145-149
14613857-12	2003	The lack of a GATA-binding consensus sequence in the Kv4.2 minimum promoter suggests that these transcription factors indirectly influence the channel gene transcription.	gata	14-18	potassium voltage-gated channel subfamily D member 2	Rattus norvegicus	53-58
12888492-4	2003	We found that str1+ is subject to negative transcriptional regulation, which is exerted through binding of Fep1 to a single GATA element in the str1+ promoter.	gata	124-128	cystathionine gamma-lyase CYS3	Saccharomyces cerevisiae S288C	144-148
12706632-8	2003	A hypothesis involving protein-protein interactions between C/EBP (pX2/BCFII) and GATA during choriogenesis is presented to explain the temporal specificity of chorion genes.	gata	82-86	chorion specific C/EBP	Bombyx mori	60-65
12650603-11	2003	It also appears to behave like a GATA-element transcription factor, since transfection of a GATA-element reporter into MTA1-expressing cells resulted in 10-20-fold increase in reporter expression over poorly MTA1-expressing cells.	gata	33-37	metastasis associated 1	Homo sapiens	119-123
12504119-7	2003	Based on these results, we propose that light controls the expression of GAPA and GAPB genes in part by regulating the binding of the same transcription factor at their GATA motifs.	gata	169-173	glyceraldehyde 3-phosphate dehydrogenase A subunit	Arabidopsis thaliana	73-77
12724402-7	2003	Quantitative electrophoretic mobility shift assays using oligonucleotides derived from the GPIX promoter containing Ets and GATA binding motifs reveal that Fli-1 and GATA-1 exhibit cooperative DNA binding in which the binding of GATA-1 to DNA is increased approximately 26-fold in the presence of Fli-1 (from 4.2 to 0.16 nM), providing a mechanism for the observed transcriptional synergy.	gata	124-128	glycoprotein IX platelet	Homo sapiens	91-95
12724402-7	2003	Quantitative electrophoretic mobility shift assays using oligonucleotides derived from the GPIX promoter containing Ets and GATA binding motifs reveal that Fli-1 and GATA-1 exhibit cooperative DNA binding in which the binding of GATA-1 to DNA is increased approximately 26-fold in the presence of Fli-1 (from 4.2 to 0.16 nM), providing a mechanism for the observed transcriptional synergy.	gata	124-128	Fli-1 proto-oncogene, ETS transcription factor	Homo sapiens	156-161
12724402-7	2003	Quantitative electrophoretic mobility shift assays using oligonucleotides derived from the GPIX promoter containing Ets and GATA binding motifs reveal that Fli-1 and GATA-1 exhibit cooperative DNA binding in which the binding of GATA-1 to DNA is increased approximately 26-fold in the presence of Fli-1 (from 4.2 to 0.16 nM), providing a mechanism for the observed transcriptional synergy.	gata	124-128	GATA binding protein 1	Homo sapiens	166-172
12724402-7	2003	Quantitative electrophoretic mobility shift assays using oligonucleotides derived from the GPIX promoter containing Ets and GATA binding motifs reveal that Fli-1 and GATA-1 exhibit cooperative DNA binding in which the binding of GATA-1 to DNA is increased approximately 26-fold in the presence of Fli-1 (from 4.2 to 0.16 nM), providing a mechanism for the observed transcriptional synergy.	gata	124-128	GATA binding protein 1	Homo sapiens	229-235
12480945-4	2003	The RXR alpha-mediated repression mapped to the proximal 147 bp of the rat ANF promoter, a region lacking a consensus retinoid response element but containing several known cardiogenic cis elements including a well characterized GATA response element.	gata	229-233	retinoid X receptor alpha	Rattus norvegicus	4-13
12480945-6	2003	Liganded RXR alpha repressed the activity of a heterologous promoter-reporter construct containing GATA-response element recognition sites in cardiac myocytes but not in several other cell types, suggesting that additional cardiac-enriched factors participate in the repression complex.	gata	99-103	retinoid X receptor alpha	Rattus norvegicus	9-18
12650603-11	2003	It also appears to behave like a GATA-element transcription factor, since transfection of a GATA-element reporter into MTA1-expressing cells resulted in 10-20-fold increase in reporter expression over poorly MTA1-expressing cells.	gata	33-37	metastasis associated 1	Homo sapiens	208-212
11788768-3	2002	The presence of GATA-like motifs in the upstream region of the Acl1.4 gene (encoding for ACP4) and the similarity in light-mediated induction to ferredoxin-A mRNA suggests a direct role of light in Acl1.4 gene activation.	gata	16-20	acyl carrier protein 4	Arabidopsis thaliana	89-93
12532156-5	2003	RESULTS: Three common MC3R variants were found: a 17C>A variant, changing Thr6-->Lys in 16%, a 241G>A variant changing Val81-->Ile in 15%, and a -239A>G substitution in the GATA binding site in 21% of the subjects.	gata	188-192	melanocortin 3 receptor	Homo sapiens	22-26
12202480-7	2002	In vitro mutational analyses of the MBP-P2 promoter showed that both the GATA-1/PU.1 synergy, and repressor activity of C/EBPepsilon(27) are mediated via protein-protein interactions through the C/EBP and/or GATA-binding sites but not the PU.1 sites.	gata	73-77	myelin basic protein	Homo sapiens	36-39
12391281-5	2002	Electrophoretic mobility shift assays (EMSAs) indicate that the putative CRE and GATA sites indeed bind cAMP response element modulator 1/c-Jun and the GATA6 protein, respectively.	gata	81-85	GATA binding protein 6	Rattus norvegicus	152-157
12200364-9	2002	Compared with wild-type GATA-1, Arg216Gln GATA-1 shows comparable affinity to single GATA sites but decreased affinity to palindromic sites.	gata	24-28	GATA binding protein 1	Homo sapiens	42-48
11978798-9	2002	Transfection with a dominant negative AP-1 construct or mutation of the AP-1, GATA, or C/EBP sites in the -272-bp IL-8 promoter construct blocked induction by nickel.	gata	78-82	C-X-C motif chemokine ligand 8	Homo sapiens	114-118
12054852-0	2002	Transcriptional activation of the BNP gene by lipopolysaccharide is mediated through GATA elements in neonatal rat cardiac myocytes.	gata	85-89	natriuretic peptide B	Rattus norvegicus	34-37
12054852-10	2002	Mutation of the GATA sequence located at -95 and -84 abolished such an induction of BNP promoter activity.	gata	16-20	natriuretic peptide B	Rattus norvegicus	84-87
12054852-12	2002	These results indicate that LPS induces the BNP gene expression through a pathway involving CD14, Rac1, p38 MAPK and GATA elements.	gata	117-121	natriuretic peptide B	Rattus norvegicus	44-47
12702322-8	2002	Furthermore, deletion analyses and mutagenesis have shown that the palindromic sequence is important for full repression of GCV2 in complex glucose-containing medium and functions in a manner that is different from control mediated by the GATA element.	gata	239-243	glycine decarboxylase subunit P	Saccharomyces cerevisiae S288C	124-128
18763064-7	2002	There is a cis-activating GATA motif in ENH of DLA-EIAV and EIAV L. Two N-linked glycosylation sites disappeared in DLA-EIAV Gp90 in comparison with that of EIAV L. A bHLH transcription factor binding consensus sequence was found in LTR of DLA-EIAV but not in EIAV L. Furthermore, there is a mutation in the stem of DLA-EIAV TAR resulting in formation of a uridine tuber.	gata	26-30	galectin 3 binding protein	Homo sapiens	125-129
11862325-3	2002	Rat B-type natriuretic peptide (BNP) gene promoter contains a region of two adjacent GATA binding sites (between -68 and -97) with high affinity for GATA-4.	gata	85-89	natriuretic peptide B	Rattus norvegicus	4-30
11862325-3	2002	Rat B-type natriuretic peptide (BNP) gene promoter contains a region of two adjacent GATA binding sites (between -68 and -97) with high affinity for GATA-4.	gata	85-89	natriuretic peptide B	Rattus norvegicus	32-35
11862325-3	2002	Rat B-type natriuretic peptide (BNP) gene promoter contains a region of two adjacent GATA binding sites (between -68 and -97) with high affinity for GATA-4.	gata	85-89	GATA binding protein 4	Rattus norvegicus	149-155
11862325-5	2002	GATA decoy oligodeoxynucleotide treatment of cardiomyocytes blocked GATA-4 DNA binding activity in electrophoretic mobility shift analysis and decreased baseline expression of cardiac natriuretic peptides and GATA-dependent promoter activity.	gata	0-4	GATA binding protein 4	Rattus norvegicus	68-74
11862325-7	2002	Mutation of GATA binding sites at -80 and -91 rat BNP promoter downregulated baseline but did not affect endothelin-1 or angiotensin II induced promoter activity.	gata	12-16	natriuretic peptide B	Rattus norvegicus	50-53
12446778-3	2002	TRPS1, the only other vertebrate protein with the GATA motif, is a large, multitype zinc finger protein that harbors a single DNA-binding GATA domain and represses transcription.	gata	50-54	transcriptional repressor GATA binding 1	Mus musculus	0-5
12446778-3	2002	TRPS1, the only other vertebrate protein with the GATA motif, is a large, multitype zinc finger protein that harbors a single DNA-binding GATA domain and represses transcription.	gata	138-142	transcriptional repressor GATA binding 1	Mus musculus	0-5
12446778-4	2002	Monoallelic TRPS1 mutations cause two dominantly inherited human developmental disorders of the hair, face, and digits, tricho-rhino-phalangeal syndrome (TRPS) types I (MIM 190350) and III (MIM 190351); missense GATA domain mutations account for the more severe type III form.	gata	212-216	transcriptional repressor GATA binding 1	Homo sapiens	12-17
12150943-5	2002	A conserved GATA site in the intergenic region was shown by site-directed mutagenesis to act as a repressor for the ABCG5 promoter.	gata	12-16	ATP binding cassette subfamily G member 5	Homo sapiens	116-121
12045237-0	2002	Targeted deletion of a high-affinity GATA-binding site in the GATA-1 promoter leads to selective loss of the eosinophil lineage in vivo.	gata	37-41	GATA binding protein 1	Mus musculus	62-68
12045237-3	2002	Here we demonstrate that deletion of a high-affinity GATA-binding site in the GATA-1 promoter, an element presumed to mediate positive autoregulation of GATA-1 expression, leads to selective loss of the eosinophil lineage.	gata	53-57	GATA binding protein 1	Mus musculus	78-84
12045237-3	2002	Here we demonstrate that deletion of a high-affinity GATA-binding site in the GATA-1 promoter, an element presumed to mediate positive autoregulation of GATA-1 expression, leads to selective loss of the eosinophil lineage.	gata	53-57	GATA binding protein 1	Mus musculus	153-159
11827958-6	2002	Overexpression of p38 kinase pathway, but not extracellular signal-regulated kinase or c-Jun N-terminal protein kinase, activated GATA-4 binding to B-type natriuretic peptide gene and induced rat B-type natriuretic peptide promoter activity via proximal GATA binding sites.	gata	130-134	mitogen activated protein kinase 14	Rattus norvegicus	18-21
11827958-7	2002	In conclusion, these findings demonstrate that activation of p38 kinase is necessary for hypertrophic agonist-induced GATA-4 binding to B-type natriuretic peptide gene and sufficient for GATA-dependent B-type natriuretic peptide gene expression.	gata	118-122	mitogen activated protein kinase 14	Rattus norvegicus	61-64
11842118-9	2002	The substitution in PS4A of a GATA-binding sequence similar to PS13, which only requires a single zinc finger domain, bound GATA-4 efficiently but did not activate the Fgf-3 promoter.	gata	30-34	GATA binding protein 4	Homo sapiens	124-130
12432220-4	2002	Closer examination revealed a cross-regulatory mechanism by which GATA-1 can control the expression of GATA-2 and vice versa, possibly via essential GATA binding sites in their cis-acting elements.	gata	66-70	GATA binding protein 2	Homo sapiens	103-109
11408486-2	2001	When nitrogen is limiting, Gln3p and Gat1p are concentrated in the nucleus where they bind GATA sequences upstream of nitrogen catabolite repression (NCR)-sensitive genes and activate their transcription.	gata	91-95	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	27-32
11606434-7	2001	The importance of these GATA elements to BNP promoter activation was further confirmed by the corresponding 38-bp oligonucleotide conferring hemodynamic stress responsiveness to a minimal BNP promoter.	gata	24-28	natriuretic peptide B	Rattus norvegicus	41-44
11606434-7	2001	The importance of these GATA elements to BNP promoter activation was further confirmed by the corresponding 38-bp oligonucleotide conferring hemodynamic stress responsiveness to a minimal BNP promoter.	gata	24-28	natriuretic peptide B	Rattus norvegicus	188-191
11606434-9	2001	In conclusion, GATA elements are necessary and sufficient to confer transcriptional activation of BNP gene in response to hemodynamic stress.	gata	15-19	natriuretic peptide B	Rattus norvegicus	98-101
11356843-2	2001	When cells are cultured with a good nitrogen source (glutamine, ammonia), Gln3p and Gat1p are restricted to the cytoplasm, whereas with a poor nitrogen source (proline), they localize to the nucleus, bind to the GATA sequences of NCR-sensitive gene promoters, and activate transcription.	gata	212-216	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	74-79
11356843-2	2001	When cells are cultured with a good nitrogen source (glutamine, ammonia), Gln3p and Gat1p are restricted to the cytoplasm, whereas with a poor nitrogen source (proline), they localize to the nucleus, bind to the GATA sequences of NCR-sensitive gene promoters, and activate transcription.	gata	212-216	Gat1p	Saccharomyces cerevisiae S288C	84-89
11408486-2	2001	When nitrogen is limiting, Gln3p and Gat1p are concentrated in the nucleus where they bind GATA sequences upstream of nitrogen catabolite repression (NCR)-sensitive genes and activate their transcription.	gata	91-95	Gat1p	Saccharomyces cerevisiae S288C	37-42
11259267-7	2001	Dax-1-mediated repression of GATA-4/SF-1 synergism did not involve direct repression of GATA-dependent transactivation, but rather, it occurred through a direct protein-protein interaction with DNA-bound SF-1.	gata	29-33	nuclear receptor subfamily 0 group B member 1	Homo sapiens	0-5
11493575-3	2001	To analyze the role played by GATAb in the regulation of the Fbp1 EcRU activity, we have replaced the GATA-binding sites GBS1, GBS2 and GBS3 in the Fbp1 EcRU with UAS sites for the yeast GAL4 activator and tested the activity of the mutagenized Fbp1 EcRUs in transgenic lines, either in the presence or absence of ubiquitously expressed GAL4.	gata	30-34	fructose 1,6-bisphosphate 1-phosphatase	Saccharomyces cerevisiae S288C	61-65
11493553-1	2001	Expression of gata1 is regulated through multiple cis-acting GATA motifs.	gata	61-65	GATA binding protein 1a	Danio rerio	14-19
11493553-5	2001	GFP reporter analyses revealed that this intron and a distal double GATA motif in the regulatory region are important for the regulation of zebrafish gata1 gene expression.	gata	68-72	GATA binding protein 1a	Danio rerio	150-155
11259267-7	2001	Dax-1-mediated repression of GATA-4/SF-1 synergism did not involve direct repression of GATA-dependent transactivation, but rather, it occurred through a direct protein-protein interaction with DNA-bound SF-1.	gata	29-33	splicing factor 1	Homo sapiens	36-40
11259267-7	2001	Dax-1-mediated repression of GATA-4/SF-1 synergism did not involve direct repression of GATA-dependent transactivation, but rather, it occurred through a direct protein-protein interaction with DNA-bound SF-1.	gata	29-33	splicing factor 1	Homo sapiens	204-208
11259267-9	2001	Because we have shown that other GATA family members also have the ability to synergize with SF-1, Dax-1 repression of GATA/SF-1 synergism may represent an important mechanism for fine-tuning the regulation of SF-1-dependent genes in multiple target tissues.	gata	33-37	splicing factor 1	Homo sapiens	93-97
11259267-9	2001	Because we have shown that other GATA family members also have the ability to synergize with SF-1, Dax-1 repression of GATA/SF-1 synergism may represent an important mechanism for fine-tuning the regulation of SF-1-dependent genes in multiple target tissues.	gata	33-37	nuclear receptor subfamily 0 group B member 1	Homo sapiens	99-104
11259267-9	2001	Because we have shown that other GATA family members also have the ability to synergize with SF-1, Dax-1 repression of GATA/SF-1 synergism may represent an important mechanism for fine-tuning the regulation of SF-1-dependent genes in multiple target tissues.	gata	33-37	splicing factor 1	Homo sapiens	124-128
11259267-9	2001	Because we have shown that other GATA family members also have the ability to synergize with SF-1, Dax-1 repression of GATA/SF-1 synergism may represent an important mechanism for fine-tuning the regulation of SF-1-dependent genes in multiple target tissues.	gata	33-37	splicing factor 1	Homo sapiens	124-128
11156886-4	2001	Gel mobility shift assays were used to analyze the trans-acting factors that interact with the GATA motifs of the BNP promoter.	gata	95-99	natriuretic peptide B	Rattus norvegicus	114-117
11073899-2	2000	In addition to the GATA sequences situated upstream of all nitrogen catabolite repression-sensitive genes that encode enzyme and transport proteins, the promoters of the GAT1, DAL80, and DEH1 genes all contain multiple GATA sequences as well.	gata	219-223	Gat1p	Saccharomyces cerevisiae S288C	170-174
11016926-6	2001	The functional cooperation between GATA-1 and PKC-epsilon displayed dependence on cellular milieu, as well as on the promoter context of GATA binding sites.	gata	35-39	protein kinase C epsilon	Homo sapiens	46-57
11073899-2	2000	In addition to the GATA sequences situated upstream of all nitrogen catabolite repression-sensitive genes that encode enzyme and transport proteins, the promoters of the GAT1, DAL80, and DEH1 genes all contain multiple GATA sequences as well.	gata	219-223	Dal80p	Saccharomyces cerevisiae S288C	176-181
11073899-2	2000	In addition to the GATA sequences situated upstream of all nitrogen catabolite repression-sensitive genes that encode enzyme and transport proteins, the promoters of the GAT1, DAL80, and DEH1 genes all contain multiple GATA sequences as well.	gata	219-223	Gzf3p	Saccharomyces cerevisiae S288C	187-191
10906145-2	2000	Gln3p binds to and Gat1p is proposed to bind to single GATA sequences; Dal80p binds to pairs of specifically oriented and spaced GATA sequences, and Dal82p binds to a pathway-specific element, UIS(ALL).	gata	129-133	Dal80p	Saccharomyces cerevisiae S288C	71-77
10788492-5	2000	Stimulation by phenylephrine caused serine phosphorylation of GATA-4 and increased its ability to bind the ET-1 GATA element.	gata	62-66	endothelin 1	Rattus norvegicus	107-111
10862620-5	2000	The GATA motifs bound GATA-1 and mutagenesis analysis revealed that the proximal one is critical for the enhancing activity.	gata	4-8	GATA binding protein 1	Homo sapiens	22-28
10851229-4	2000	Here, we show that GATA-6 bound to a GATA-like motif (-810/-805) within the rat Sm-MHC promoter in a sequence-specific manner and activated this promoter through this site.	gata	19-23	myosin heavy chain 11	Rattus norvegicus	80-86
10799523-1	2000	GATA family activators (Gln3p and Gat1p) and repressors (Dal80p and Deh1p) regulate nitrogen catabolite repression (NCR)-sensitive transcription in Saccharomyces cerevisiae presumably via their competitive binding to the GATA sequences upstream of NCR-sensitive genes.	gata	0-4	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	24-29
10799523-1	2000	GATA family activators (Gln3p and Gat1p) and repressors (Dal80p and Deh1p) regulate nitrogen catabolite repression (NCR)-sensitive transcription in Saccharomyces cerevisiae presumably via their competitive binding to the GATA sequences upstream of NCR-sensitive genes.	gata	0-4	Gat1p	Saccharomyces cerevisiae S288C	34-39
10799523-1	2000	GATA family activators (Gln3p and Gat1p) and repressors (Dal80p and Deh1p) regulate nitrogen catabolite repression (NCR)-sensitive transcription in Saccharomyces cerevisiae presumably via their competitive binding to the GATA sequences upstream of NCR-sensitive genes.	gata	0-4	Dal80p	Saccharomyces cerevisiae S288C	57-63
10799523-1	2000	GATA family activators (Gln3p and Gat1p) and repressors (Dal80p and Deh1p) regulate nitrogen catabolite repression (NCR)-sensitive transcription in Saccharomyces cerevisiae presumably via their competitive binding to the GATA sequences upstream of NCR-sensitive genes.	gata	0-4	Gzf3p	Saccharomyces cerevisiae S288C	68-73
10799523-1	2000	GATA family activators (Gln3p and Gat1p) and repressors (Dal80p and Deh1p) regulate nitrogen catabolite repression (NCR)-sensitive transcription in Saccharomyces cerevisiae presumably via their competitive binding to the GATA sequences upstream of NCR-sensitive genes.	gata	221-225	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	24-29
10799523-1	2000	GATA family activators (Gln3p and Gat1p) and repressors (Dal80p and Deh1p) regulate nitrogen catabolite repression (NCR)-sensitive transcription in Saccharomyces cerevisiae presumably via their competitive binding to the GATA sequences upstream of NCR-sensitive genes.	gata	221-225	Gat1p	Saccharomyces cerevisiae S288C	34-39
10799523-1	2000	GATA family activators (Gln3p and Gat1p) and repressors (Dal80p and Deh1p) regulate nitrogen catabolite repression (NCR)-sensitive transcription in Saccharomyces cerevisiae presumably via their competitive binding to the GATA sequences upstream of NCR-sensitive genes.	gata	221-225	Dal80p	Saccharomyces cerevisiae S288C	57-63
10799523-1	2000	GATA family activators (Gln3p and Gat1p) and repressors (Dal80p and Deh1p) regulate nitrogen catabolite repression (NCR)-sensitive transcription in Saccharomyces cerevisiae presumably via their competitive binding to the GATA sequences upstream of NCR-sensitive genes.	gata	221-225	Gzf3p	Saccharomyces cerevisiae S288C	68-73
10788492-3	2000	Using transient transfection assays in primary cardiac myocytes from neonatal rats, we show here that the GATA element in the rat ET-1 promoter was required for phenylephrine-stimulated ET-1 transcription.	gata	106-110	endothelin 1	Rattus norvegicus	130-134
10788492-3	2000	Using transient transfection assays in primary cardiac myocytes from neonatal rats, we show here that the GATA element in the rat ET-1 promoter was required for phenylephrine-stimulated ET-1 transcription.	gata	106-110	endothelin 1	Rattus norvegicus	186-190
10625644-3	2000	In this work, a consensus GATA-binding site (GBS) was identified at positions -69 to -64 of the mouse SP-A gene.	gata	26-30	surfactant associated protein A1	Mus musculus	102-106
10588863-5	1999	GATA-dependent regulatory sequences of the Nkx2.5 gene that implicate GATA-4/5/6 as upstream positive regulators were described recently.	gata	0-4	NK2 homeobox 5 S homeolog	Xenopus laevis	43-49
10588863-5	1999	GATA-dependent regulatory sequences of the Nkx2.5 gene that implicate GATA-4/5/6 as upstream positive regulators were described recently.	gata	0-4	GATA binding protein 4 L homeolog	Xenopus laevis	70-76
10559172-1	1999	Dal82p binds to the UIS(ALL) sites of allophanate-induced genes of the allantoin-degradative pathway and functions synergistically with the GATA family Gln3p and Gat1p transcriptional activators that are responsible for nitrogen catabolite repression-sensitive gene expression.	gata	140-144	Dal82p	Saccharomyces cerevisiae S288C	0-6
10559172-1	1999	Dal82p binds to the UIS(ALL) sites of allophanate-induced genes of the allantoin-degradative pathway and functions synergistically with the GATA family Gln3p and Gat1p transcriptional activators that are responsible for nitrogen catabolite repression-sensitive gene expression.	gata	140-144	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	152-157
10559172-8	1999	This synergism is unlike all other known instances of Dal82p synergism, namely, that with the GATA family transcription activators Gln3p and Gat1p, which occurs only in the presence of an inducer.	gata	94-98	Dal82p	Saccharomyces cerevisiae S288C	54-60
10559172-8	1999	This synergism is unlike all other known instances of Dal82p synergism, namely, that with the GATA family transcription activators Gln3p and Gat1p, which occurs only in the presence of an inducer.	gata	94-98	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	131-136
10523648-3	1999	We found that an HS2 element mutated in its GATA motif failed to remodel the epsilon-globin promoter or activate transcription yet HS2 nuclease accessibility did not change.	gata	44-48	spectrin beta, erythrocytic	Homo sapiens	17-20
10501969-7	1999	Functional studies with recombinant GATA-4, -5, and -6 proteins show that GATA-5 has preferential affinity for a subset of GATA elements found on cardiac promoters and differentially activate cardiac gene transcription.	gata	36-40	GATA binding protein 5	Rattus norvegicus	74-80
10514435-7	1999	In vivo deletion and site-directed mutation analyses confirm that one GATA element in mtl-1 and two in mtl-2 are required for transcription.	gata	70-74	Metallothionein-1	Caenorhabditis elegans	86-91
10514435-11	1999	These results indicate that cell-specific transcription of the C. elegans metallothionein genes is regulated by the binding of ELT-2 to GATA elements in these promoters.	gata	136-140	Transcription factor elt-2	Caenorhabditis elegans	127-132
10597043-1	1999	The Caenorhabditis elegans ELT-1 protein, a homolog of the vertebrate GATA transcription factor family, is a transcription activator that can recognize the GATA motif.	gata	70-74	Transcription factor elt-1	Caenorhabditis elegans	27-32
10597043-6	1999	To investigate the possible target genes for the ELT-1 protein in the germ line, the ELT-1 protein was expressed and tested for its binding specificity to the GATA motif that is present in the promoter region of the C. elegans major sperm protein genes.	gata	159-163	Transcription factor elt-1	Caenorhabditis elegans	49-54
10597043-6	1999	To investigate the possible target genes for the ELT-1 protein in the germ line, the ELT-1 protein was expressed and tested for its binding specificity to the GATA motif that is present in the promoter region of the C. elegans major sperm protein genes.	gata	159-163	Transcription factor elt-1	Caenorhabditis elegans	85-90
10597043-8	1999	Mutational analysis showed that the GATC core sequence was necessary for strong transactivation of the reporter gene, and that the combination of GATC and GATA motif resulted in a stronger transactivation by ELT-1 than either the duplicated GATC or GATA motif.	gata	155-159	Transcription factor elt-1	Caenorhabditis elegans	208-213
10597043-8	1999	Mutational analysis showed that the GATC core sequence was necessary for strong transactivation of the reporter gene, and that the combination of GATC and GATA motif resulted in a stronger transactivation by ELT-1 than either the duplicated GATC or GATA motif.	gata	249-253	Transcription factor elt-1	Caenorhabditis elegans	208-213
9834187-0	1999	Control of early cardiac-specific transcription of Nkx2-5 by a GATA-dependent enhancer.	gata	63-67	NK2 homeobox 5	Mus musculus	51-57
10524205-4	1999	Transcriptional reporter assays in Ba/F3 cells revealed that two AP-1 sites, a GATA motif, and an Ets site are required for induction of DUB-1 enhancer activity.	gata	79-83	ubiquitin specific peptidase 17-like A	Mus musculus	137-142
10438731-3	1999	Further analysis of the MBP promoter region identified a C/EBP (CCAAT/enhancer-binding protein) consensus binding site 6 bp upstream of the functional GATA-binding site in the MBP gene.	gata	151-155	myelin basic protein	Homo sapiens	24-27
10438731-3	1999	Further analysis of the MBP promoter region identified a C/EBP (CCAAT/enhancer-binding protein) consensus binding site 6 bp upstream of the functional GATA-binding site in the MBP gene.	gata	151-155	myelin basic protein	Homo sapiens	176-179
10438731-6	1999	Furthermore, we have demonstrated that both C/EBPbeta and GATA-1 can bind simultaneously to the C/EBP- and GATA-binding sites in the MBP promoter.	gata	58-62	myelin basic protein	Homo sapiens	133-136
10395794-10	1999	Electrophoretic mobility shift assay revealed that GATA-1 could bind to the -29/-24 GATA motif and this was confirmed by the observation that the nuclear protein bound to the motif was supershifted by an anti-GATA-1 monoclonal antibody.	gata	51-55	GATA binding protein 1	Mus musculus	209-215
10207004-7	1999	The upstream sequence of the cloned PGRP gene was shown to contain putative cis-regulatory elements similar to the NF-kappaB-like element, interferon-response half-element, and GATA motif element, which have been found in the promoters of the acute phase protein genes of mammals and insects.	gata	177-181	peptidoglycan recognition protein	Bombyx mori	36-40
10075997-2	1999	Previous functional analysis demonstrated that the repression of the GPB promoter is determined by the binding of a ubiquitous factor which recognizes a GATA motif centered at position -75.	gata	153-157	glycophorin B (MNS blood group)	Homo sapiens	69-72
10075997-4	1999	Here, we have identified the Ku70 protein as a candidate GPB repressor DNA binding subunit through the screening of a human HeLa expression library using the -75 GATA sequence as bait (one-hybrid method).	gata	162-166	X-ray repair cross complementing 6	Homo sapiens	29-33
10075997-4	1999	Here, we have identified the Ku70 protein as a candidate GPB repressor DNA binding subunit through the screening of a human HeLa expression library using the -75 GATA sequence as bait (one-hybrid method).	gata	162-166	glycophorin B (MNS blood group)	Homo sapiens	57-60
9834187-9	1999	These results reveal a novel GATA-dependent mechanism for activation of Nkx2-5 transcription in the developing heart and indicate that regulation of Nkx2-5 is controlled in a modular manner, with multiple regulatory regions responding to distinct transcriptional networks in different compartments of the developing heart.	gata	29-33	NK2 homeobox 5	Mus musculus	72-78
9834187-9	1999	These results reveal a novel GATA-dependent mechanism for activation of Nkx2-5 transcription in the developing heart and indicate that regulation of Nkx2-5 is controlled in a modular manner, with multiple regulatory regions responding to distinct transcriptional networks in different compartments of the developing heart.	gata	29-33	NK2 homeobox 5	Mus musculus	149-155
9693032-2	1998	The NOTCH4 locus contains a TATA-less promoter with two putative transcription initiation sites (Inr), three RBP-Jkappa sites, and two GATA recognition sites.	gata	135-139	notch receptor 4	Homo sapiens	4-10
9737959-5	1998	Although this conserved element imparts high level transcription to a heterologous promoter in all lines examined, erythroid specificity is retained only when it is fused to the proximal EKLF promoter, which contains an important GATA site.	gata	230-234	Kruppel like factor 1	Homo sapiens	187-191
9819382-7	1998	Promoter analysis revealed that a GATA site in a cryptic promoter in the second intron was essential and sufficient for the TAL1- and LMO-dependent transcriptional activation, and GATA3 binds to this site.	gata	34-38	T cell acute lymphocytic leukemia 1	Mus musculus	124-128
9819382-7	1998	Promoter analysis revealed that a GATA site in a cryptic promoter in the second intron was essential and sufficient for the TAL1- and LMO-dependent transcriptional activation, and GATA3 binds to this site.	gata	34-38	GATA binding protein 3	Mus musculus	180-185
9791119-2	1998	Thus far, Gln3p, Dal80p, and Deh1p have been shown to bind to GATA sequences in NCR-sensitive promoters, in some cases to exactly the same GATA sequences.	gata	62-66	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	10-15
9791119-2	1998	Thus far, Gln3p, Dal80p, and Deh1p have been shown to bind to GATA sequences in NCR-sensitive promoters, in some cases to exactly the same GATA sequences.	gata	62-66	Dal80p	Saccharomyces cerevisiae S288C	17-23
9791119-2	1998	Thus far, Gln3p, Dal80p, and Deh1p have been shown to bind to GATA sequences in NCR-sensitive promoters, in some cases to exactly the same GATA sequences.	gata	62-66	Gzf3p	Saccharomyces cerevisiae S288C	29-34
9791119-2	1998	Thus far, Gln3p, Dal80p, and Deh1p have been shown to bind to GATA sequences in NCR-sensitive promoters, in some cases to exactly the same GATA sequences.	gata	139-143	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	10-15
9791119-2	1998	Thus far, Gln3p, Dal80p, and Deh1p have been shown to bind to GATA sequences in NCR-sensitive promoters, in some cases to exactly the same GATA sequences.	gata	139-143	Dal80p	Saccharomyces cerevisiae S288C	17-23
9791119-2	1998	Thus far, Gln3p, Dal80p, and Deh1p have been shown to bind to GATA sequences in NCR-sensitive promoters, in some cases to exactly the same GATA sequences.	gata	139-143	Gzf3p	Saccharomyces cerevisiae S288C	29-34
9753664-6	1998	Consistent with this postulation, we found that the promoter region of the isolated BMP-4 genomic DNA includes several consensus binding sites for transcriptional regulators functioning under BMP-4 signaling such as GATA binding and ventralizing homeobox genes.	gata	216-220	bone morphogenetic protein 4 L homeolog	Xenopus laevis	84-89
9753664-6	1998	Consistent with this postulation, we found that the promoter region of the isolated BMP-4 genomic DNA includes several consensus binding sites for transcriptional regulators functioning under BMP-4 signaling such as GATA binding and ventralizing homeobox genes.	gata	216-220	bone morphogenetic protein 4 L homeolog	Xenopus laevis	192-197
9753664-7	1998	In a functional assay we found that the GATA binding and ventral homeobox proteins can positively modulate BMP-4 promoter activity.	gata	40-44	bone morphogenetic protein 4 L homeolog	Xenopus laevis	107-112
9724651-2	1998	Using immunoprecipitation of genomic fragments bound to TAL-1 in the chromatin of murine erythro-leukemia (MEL) cells, we found that 10% of the immunoselected fragments contained a CAGATG or a CAGGTG E-box, followed by a GATA site.	gata	221-225	T cell acute lymphocytic leukemia 1	Mus musculus	56-61
9724651-3	1998	We studied one of these fragments containing two E-boxes, CAGATG and CAGGTC, followed by a GATA motif, and showed that TAL-1 binds to the CAGGTG E-box with an affinity modulated by the CAGATG or the GATA site, and that the CAGGTG-GATA motif exhibits positive transcriptional activity in MEL but not in HeLa cells.	gata	91-95	TAL bHLH transcription factor 1, erythroid differentiation factor	Homo sapiens	119-124
9724651-3	1998	We studied one of these fragments containing two E-boxes, CAGATG and CAGGTC, followed by a GATA motif, and showed that TAL-1 binds to the CAGGTG E-box with an affinity modulated by the CAGATG or the GATA site, and that the CAGGTG-GATA motif exhibits positive transcriptional activity in MEL but not in HeLa cells.	gata	199-203	TAL bHLH transcription factor 1, erythroid differentiation factor	Homo sapiens	119-124
9724651-3	1998	We studied one of these fragments containing two E-boxes, CAGATG and CAGGTC, followed by a GATA motif, and showed that TAL-1 binds to the CAGGTG E-box with an affinity modulated by the CAGATG or the GATA site, and that the CAGGTG-GATA motif exhibits positive transcriptional activity in MEL but not in HeLa cells.	gata	199-203	TAL bHLH transcription factor 1, erythroid differentiation factor	Homo sapiens	119-124
9724651-6	1998	These results establish that TAL-1 is likely to activate its target genes through a complex that binds an E-box-GATA motif and define the first gene regulated by TAL-1.	gata	112-116	TAL bHLH transcription factor 1, erythroid differentiation factor	Homo sapiens	29-34
9642238-10	1998	The GATA motif bound GATA-1 in vitro.	gata	4-8	GATA binding protein 1	Homo sapiens	21-27
9634475-8	1998	In particular, a GATA/c-Ets motive was identified in a short segment homologous to the mouse CD4 distal enhancer, suggesting that LAG-3, which is embedded in the CD4 locus, may be controlled by some CD4 regulatory elements.	gata	17-21	CD4 antigen	Mus musculus	93-96
9634475-8	1998	In particular, a GATA/c-Ets motive was identified in a short segment homologous to the mouse CD4 distal enhancer, suggesting that LAG-3, which is embedded in the CD4 locus, may be controlled by some CD4 regulatory elements.	gata	17-21	lymphocyte-activation gene 3	Mus musculus	130-135
9571201-4	1998	Within the 5" flanking region we identified a putative binding site for NRF-2, a GATA- and GC-box element.	gata	81-85	NFE2 like bZIP transcription factor 2	Homo sapiens	72-77
9634475-8	1998	In particular, a GATA/c-Ets motive was identified in a short segment homologous to the mouse CD4 distal enhancer, suggesting that LAG-3, which is embedded in the CD4 locus, may be controlled by some CD4 regulatory elements.	gata	17-21	CD4 antigen	Mus musculus	162-165
9634475-8	1998	In particular, a GATA/c-Ets motive was identified in a short segment homologous to the mouse CD4 distal enhancer, suggesting that LAG-3, which is embedded in the CD4 locus, may be controlled by some CD4 regulatory elements.	gata	17-21	CD4 antigen	Mus musculus	162-165
9659934-1	1998	The Caenorhabditis elegans elt-2 gene encodes a single-finger GATA factor, previously cloned by virtue of its binding to a tandem pair of GATA sites that control the gut-specific ges-1 esterase gene.	gata	62-66	Transcription factor elt-2	Caenorhabditis elegans	27-32
9659934-1	1998	The Caenorhabditis elegans elt-2 gene encodes a single-finger GATA factor, previously cloned by virtue of its binding to a tandem pair of GATA sites that control the gut-specific ges-1 esterase gene.	gata	62-66	Gut esterase 1	Caenorhabditis elegans	179-184
9600835-7	1998	Cloning of the metchnikowin gene revealed the presence in the 5" flanking region of several putative cis-regulatory motifs characterized in the promoters of insect immune genes: namely, Rel sites, GATA motifs, interferon consensus response elements and NF-IL6 response elements.	gata	197-201	Metchnikowin	Drosophila melanogaster	15-27
9628819-3	1998	Several putative transcription factor-binding sites were identified in each of the urocortin promoters, including a TATA box, a cyclic AMP response element (CRE), GATA-binding sites, and a C/EBP-binding site as well as a Brn-2-binding site(s).	gata	163-167	urocortin	Homo sapiens	83-92
9486185-5	1998	Mutational analysis of the LUE demonstrated that bases contained within a GATA consensus motif are critical for both CCP binding and transcription from the LPH promoter.	gata	74-78	lactase	Homo sapiens	156-159
9498775-11	1998	Taken together, our results provide evidence that GATA-related factors may be involved in Th2-specific expression of the IL-5 gene.	gata	50-54	heart and neural crest derivatives expressed 2	Mus musculus	90-93
9498775-11	1998	Taken together, our results provide evidence that GATA-related factors may be involved in Th2-specific expression of the IL-5 gene.	gata	50-54	interleukin 5	Mus musculus	121-125
9473510-8	1998	The core promoter of RH50 gene was located within 68bp length from the translation start position, which included an inverse GATA motif, although obvious motifs for Sp1 or erythroid Kruppel-like factor were lacking.	gata	125-129	Rh associated glycoprotein	Homo sapiens	21-25
9305891-2	1997	The P1 region of the mouse TSHbeta promoter (-133 to -88) region interacts with Pit-1 and an additional 50-kDa factor at an adjacent site that resembles a consensus GATA binding site.	gata	165-169	thyroid stimulating hormone, beta subunit	Mus musculus	27-34
9403619-10	1997	A GATA element within beta-MHC sequences -303/-197 plays a role in the transcriptional activation of this gene by aortic constriction.	gata	2-6	myosin heavy chain 7	Rattus norvegicus	22-30
9761670-0	1998	Regulation of the Caenorhabditis elegans gut cysteine protease gene cpr-1: requirement for GATA motifs.	gata	91-95	Gut-specific cysteine proteinase	Caenorhabditis elegans	68-73
9761670-6	1998	A concatemer of the cpr-1 -147 GATA motif placed upstream of minimal promoter/lac Z reporter gene constructs results in strong reporter gene expression in gut cells of larval stages and also in embryos.	gata	31-35	Gut-specific cysteine proteinase	Caenorhabditis elegans	20-25
9401021-2	1997	All four proteins contain GATA-type zinc finger domains, and three of them (Gln3p, Dal80p, and Deh1p) have been shown to bind to GATA sequences situated upstream of genes whose expression is sensitive to nitrogen catabolite repression (NCR).	gata	26-30	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	76-81
9401021-2	1997	All four proteins contain GATA-type zinc finger domains, and three of them (Gln3p, Dal80p, and Deh1p) have been shown to bind to GATA sequences situated upstream of genes whose expression is sensitive to nitrogen catabolite repression (NCR).	gata	26-30	Dal80p	Saccharomyces cerevisiae S288C	83-89
9401021-2	1997	All four proteins contain GATA-type zinc finger domains, and three of them (Gln3p, Dal80p, and Deh1p) have been shown to bind to GATA sequences situated upstream of genes whose expression is sensitive to nitrogen catabolite repression (NCR).	gata	26-30	Gzf3p	Saccharomyces cerevisiae S288C	95-100
9249061-3	1997	Putative transcription factor binding sites that might be significant for THBS2 regulation included p53, NF-kappaB, Spl, Myc-CF1, NF-Y, CF1, AP1, and GATA sites.	gata	150-154	thrombospondin 2	Homo sapiens	74-79
9231805-11	1997	In light of these findings, the established role of other GATA-binding proteins in hematopoetic cell differentiation and apoptosis, and the presence of conserved GATA motifs in the promoters of genes expressed selectively in ovary, we propose that GATA-4 and GATA-6 play distinct roles in follicular development and luteinization.	gata	58-62	GATA binding protein 4	Mus musculus	248-254
9231805-11	1997	In light of these findings, the established role of other GATA-binding proteins in hematopoetic cell differentiation and apoptosis, and the presence of conserved GATA motifs in the promoters of genes expressed selectively in ovary, we propose that GATA-4 and GATA-6 play distinct roles in follicular development and luteinization.	gata	162-166	GATA binding protein 4	Mus musculus	248-254
9211887-9	1997	Contained in this region is a consensus GATA motif, suggesting that a member of the GATA family of DNA-binding proteins is involved in the cell-specific regulation of the GIP gene.	gata	40-44	gastric inhibitory polypeptide	Mus musculus	171-174
9125153-4	1997	Reverse-transcription PCR using dissected nephron segments revealed that rat GATA-3 but not GATA-2 was expressed in collecting ducts, thus indicating that GATA-3 could interact with GATA motifs in the AQP-2 promoter.	gata	77-81	GATA binding protein 3	Rattus norvegicus	155-161
9125153-4	1997	Reverse-transcription PCR using dissected nephron segments revealed that rat GATA-3 but not GATA-2 was expressed in collecting ducts, thus indicating that GATA-3 could interact with GATA motifs in the AQP-2 promoter.	gata	77-81	aquaporin 2	Rattus norvegicus	201-206
9028940-8	1997	An electrophoretic mobility shift assay (EMSA) showed that in EPO-stimulated UT-7 cells, the dynamic changes in EPOR gene expression paralleled the GATA-1 DNA-binding activity to the oligonucleotide probe containing a GATA-binding site located at the promoter region of the EPOR gene.	gata	148-152	erythropoietin	Homo sapiens	62-65
9028940-8	1997	An electrophoretic mobility shift assay (EMSA) showed that in EPO-stimulated UT-7 cells, the dynamic changes in EPOR gene expression paralleled the GATA-1 DNA-binding activity to the oligonucleotide probe containing a GATA-binding site located at the promoter region of the EPOR gene.	gata	148-152	erythropoietin receptor	Homo sapiens	112-116
7760810-7	1995	ER-mediated repression of GATA-1 activity occurs on an artificial promoter containing a single GATA-binding site, as well as in the context of an intact promoter which is normally regulated by GATA-1.	gata	26-30	GATA binding protein 1	Homo sapiens	193-199
8977242-8	1996	Although our functional approach does not yet indicate the precise sequences required for erythroid induction, the AE1 gene upstream region contains potential GATA sites at -154, -141, and -60; an E-box at -163; CACCC or GGTGG motifs at -188, -121, and -88; and an AP-1/NF-E2-like site at -42.	gata	159-163	solute carrier family 4 (anion exchanger), member 1	Mus musculus	115-118
8901135-2	1996	An E. coli-expressed NIT2/beta-Gal fusion protein binds specifically to DNA in vitro by recognizing GATA core elements.	gata	100-104	nitrilase family, member 2	Mus musculus	21-25
8901135-4	1996	The native NIT2 protein in nuclear extracts binds with high affinity to DNA fragments which contain two GATA elements, weakly to fragments with a single GATA element, and fails to bind to DNAs which lack these sequences.	gata	104-108	nitrilase family, member 2	Mus musculus	11-15
8901135-4	1996	The native NIT2 protein in nuclear extracts binds with high affinity to DNA fragments which contain two GATA elements, weakly to fragments with a single GATA element, and fails to bind to DNAs which lack these sequences.	gata	153-157	nitrilase family, member 2	Mus musculus	11-15
7568152-0	1995	Role of the GATA factors Gln3p and Nil1p of Saccharomyces cerevisiae in the expression of nitrogen-regulated genes.	gata	12-16	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	25-30
8690723-4	1995	Deletion analysis of the distal GATA site and its neighboring sequence and DNase-I footprinting/EMSA (electrophoretic mobility shift assay) analysis indicated that induced nuclear factor binding to GATA-1 and its neighboring sequence may be required for expression during MEL cell differentiation induced by dimethyl sulfoxide treatment.	gata	32-36	GATA binding protein 1	Mus musculus	198-204
7782329-3	1995	The longest open reading frame in the elt-2 cDNA codes for a protein of M(r) 47,000 with a single zinc finger domain, similar (approximately 75% amino acid identity) to the C-terminal fingers of all other two-fingered GATA factors isolated to date.	gata	218-222	Transcription factor elt-2	Caenorhabditis elegans	38-43
7782329-5	1995	An upstream region in the ELT-2 protein with the sequence C-X2-C-X16-C-X2-C has some of the characteristics of a zinc finger domain but is highly diverged from the zinc finger domains of other GATA factors.	gata	193-197	Transcription factor elt-2	Caenorhabditis elegans	26-31
7782329-7	1995	The genomic clone for elt-2 has been characterized and mapped near the center of the C. elegans X chromosome, ELT-2 protein, produced by in vitro transcription-translation, binds to ges-1 GATA-containing oligonucleotides similar to a factor previously identified in C. elegans embryo extracts, both as assayed by electrophoretic migration and by competition with wild type and mutant oligonucleotides.	gata	188-192	Transcription factor elt-2	Caenorhabditis elegans	22-27
7782329-7	1995	The genomic clone for elt-2 has been characterized and mapped near the center of the C. elegans X chromosome, ELT-2 protein, produced by in vitro transcription-translation, binds to ges-1 GATA-containing oligonucleotides similar to a factor previously identified in C. elegans embryo extracts, both as assayed by electrophoretic migration and by competition with wild type and mutant oligonucleotides.	gata	188-192	Transcription factor elt-2	Caenorhabditis elegans	110-115
7782329-7	1995	The genomic clone for elt-2 has been characterized and mapped near the center of the C. elegans X chromosome, ELT-2 protein, produced by in vitro transcription-translation, binds to ges-1 GATA-containing oligonucleotides similar to a factor previously identified in C. elegans embryo extracts, both as assayed by electrophoretic migration and by competition with wild type and mutant oligonucleotides.	gata	188-192	Gut esterase 1	Caenorhabditis elegans	182-187
8896456-2	1996	In this study, we characterize an essential upstream IL-2 response element that contains both consensus and non-consensus GAS motifs, two putative Ets binding sites (EBS), one of which overlaps the consensus GAS motif, and a GATA motif, which overlaps the non-consensus GAS motif.	gata	225-229	interleukin 2	Homo sapiens	53-57
8703016-9	1996	The mutation changes a GATA consensus binding site, disrupts GATA-1 binding to the mutated site, and decreases promoter activity by 84%.	gata	23-27	GATA binding protein 1	Homo sapiens	61-67
11012226-7	1996	GATA-1 binds with low affinity to a unique GATA motif at -70 in the MPL promoter, and destruction of this site yields only a modest decrease in expression level in human erythroleukemia (HEL) cells.	gata	0-4	MPL proto-oncogene, thrombopoietin receptor	Homo sapiens	68-71
7473742-1	1995	The GATA motif (WGATAR) is found in the promoter regions of numerous Caenorhabditis elegans genes, including two intestine-specific genes, vit-2 and ges-1, in which it has been shown to be required for promoter function.	gata	4-8	Vitellogenin-2	Caenorhabditis elegans	139-144
7473742-1	1995	The GATA motif (WGATAR) is found in the promoter regions of numerous Caenorhabditis elegans genes, including two intestine-specific genes, vit-2 and ges-1, in which it has been shown to be required for promoter function.	gata	4-8	Gut esterase 1	Caenorhabditis elegans	149-154
7473742-9	1995	The deleted ELT-1 protein containing only the C-terminal Zn finger was sufficient for activation in response to GATA, but both fingers were required for activation at GATC.	gata	112-116	Transcription factor elt-1	Caenorhabditis elegans	12-17
7639699-8	1995	In addition, sequences described in the Drosophila melanogaster Sgs-3 gene as being involved in its salivary gland-specific expression as well as two putative OTF- and GATA-binding elements were also found.	gata	168-172	Salivary gland secretion 3	Drosophila melanogaster	64-69
7649372-0	1995	A gut-to-pharynx/tail switch in embryonic expression of the Caenorhabditis elegans ges-1 gene centers on two GATA sequences.	gata	109-113	Gut esterase 1	Caenorhabditis elegans	83-88
7890725-7	1995	Gel shift competition experiments and transactivation studies revealed that this functional activity is mediated via binding at a GATA-binding site in the WT1 enhancer.	gata	130-134	WT1 transcription factor	Homo sapiens	155-158
7717974-4	1995	Gel-shift experiments and antibody binding studies demonstrate that: (1) GATA-4 is the major GATA-binding protein activity in differentiated F9 cells, and (2) GATA-4 binds to consensus GATA motifs in the retinoic acid-responsive portion of the J6 promoter.	gata	73-77	GATA binding protein 4	Mus musculus	159-165
8045902-2	1994	The deduced sequences of the DAL80 and GLN3 proteins contain a zinc finger motif homologous to those shown to bind GATA sequences.	gata	115-119	Dal80p	Saccharomyces cerevisiae S288C	29-34
7853477-5	1995	Two of the required elements, GATA (at -114) and CACGTG (at -104), were previously shown to specifically bind host transcription factors and activate transcription from the TATA-dependent wild-type gp64 efp promoter.	gata	30-34	gp64	Orgyia pseudotsugata multiple nucleopolyhedrovirus	198-202
7808401-2	1994	NIT2 binding sites in the promoter regions of nit3, alc and lao have at least two GATA sequence elements.	gata	82-86	putative hydrolase	Saccharomyces cerevisiae S288C	0-4
7808401-3	1994	We have examined the binding affinity of the NIT2 protein for the yeast DAL5 wild-type upstream activation sequence UASNTR, which contains two GATA elements, and for a series of mutated binding sites, each differing from the wild-type site by a single base.	gata	143-147	putative hydrolase	Saccharomyces cerevisiae S288C	45-49
7808401-5	1994	In contrast, nearly all substitutions within the GATA elements almost completely eliminated NIT2 binding, demonstrating the importance of the GATA sequence for NIT2 binding.	gata	49-53	putative hydrolase	Saccharomyces cerevisiae S288C	92-96
7808401-5	1994	In contrast, nearly all substitutions within the GATA elements almost completely eliminated NIT2 binding, demonstrating the importance of the GATA sequence for NIT2 binding.	gata	49-53	putative hydrolase	Saccharomyces cerevisiae S288C	160-164
7808401-5	1994	In contrast, nearly all substitutions within the GATA elements almost completely eliminated NIT2 binding, demonstrating the importance of the GATA sequence for NIT2 binding.	gata	142-146	putative hydrolase	Saccharomyces cerevisiae S288C	92-96
7808401-5	1994	In contrast, nearly all substitutions within the GATA elements almost completely eliminated NIT2 binding, demonstrating the importance of the GATA sequence for NIT2 binding.	gata	142-146	putative hydrolase	Saccharomyces cerevisiae S288C	160-164
8045902-2	1994	The deduced sequences of the DAL80 and GLN3 proteins contain a zinc finger motif homologous to those shown to bind GATA sequences.	gata	115-119	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	39-43
8045902-4	1994	We demonstrate here that the GATA-containing sites upstream of UGA4 required for optimal GLN3-dependent transcriptional activation also mediate DAL80 protein binding in vitro and DAL80-responsive regulation in vivo.	gata	29-33	Uga4p	Saccharomyces cerevisiae S288C	63-67
8045902-4	1994	We demonstrate here that the GATA-containing sites upstream of UGA4 required for optimal GLN3-dependent transcriptional activation also mediate DAL80 protein binding in vitro and DAL80-responsive regulation in vivo.	gata	29-33	nitrogen-responsive transcriptional regulator GLN3	Saccharomyces cerevisiae S288C	89-93
8045902-4	1994	We demonstrate here that the GATA-containing sites upstream of UGA4 required for optimal GLN3-dependent transcriptional activation also mediate DAL80 protein binding in vitro and DAL80-responsive regulation in vivo.	gata	29-33	Dal80p	Saccharomyces cerevisiae S288C	144-149
8045902-4	1994	We demonstrate here that the GATA-containing sites upstream of UGA4 required for optimal GLN3-dependent transcriptional activation also mediate DAL80 protein binding in vitro and DAL80-responsive regulation in vivo.	gata	29-33	Dal80p	Saccharomyces cerevisiae S288C	179-184
8400237-8	1993	The CLC promoter sequence contains two consensus GATA binding sites, a purine-rich sequence that presents potential binding sites for PU.1, a member of the ets family of genes, as well as sequences described in other myeloid-specific promoters.	gata	49-53	Charcot-Leyden crystal galectin	Homo sapiens	4-7
8007990-5	1994	We recently found two putative GATA-binding sites within the proximal enhancer of the alpha-MHC gene, suggesting that GATA-4 might regulate its expression.	gata	31-35	myosin heavy chain 6	Homo sapiens	86-95
8007990-5	1994	We recently found two putative GATA-binding sites within the proximal enhancer of the alpha-MHC gene, suggesting that GATA-4 might regulate its expression.	gata	31-35	GATA binding protein 4	Homo sapiens	118-124
8007990-6	1994	In this study, we establish that GATA-4 interacts with the alpha-MHC GATA sites to stimulate cardiac muscle-specific expression.	gata	33-37	myosin heavy chain 6	Homo sapiens	59-68
8007990-8	1994	GATA-4-dependent enhancement of activity from a heterologous promoter was mediated through the alpha-MHC GATA sites.	gata	0-4	myosin heavy chain 6	Homo sapiens	95-104
8200477-6	1994	Factors that bind to double-stranded oligonucleotides containing the ges-1 GATA sequences are present predominantly in nuclear extracts of embryos but are found neither in cytoplasmic nor in nuclear extracts of unfertilized oocytes.	gata	75-79	Gut esterase 1	Caenorhabditis elegans	69-74
8200477-7	1994	Two proteins, of 43 and 60 kDa, can be uv-crosslinked to double-stranded oligonucleotides containing the ges-1 GATA sequences.	gata	111-115	Gut esterase 1	Caenorhabditis elegans	105-110
8164667-5	1994	Cloning and functional analysis of the rat BNP upstream sequences revealed unexpected structural resemblance to erythroid but not to muscle-specific promoters and enhancers, including a requirement for regulatory elements containing GATA motifs.	gata	233-237	natriuretic peptide B	Rattus norvegicus	43-46
8164667-8	1994	Within the heart, GATA transcripts are localized in ANP- and BNP-expressing myocytes, and forced expression of the GATA protein in heterologous cells markedly activates transcription from the natural cardiac muscle-specific ANP and BNP promoters.	gata	18-22	natriuretic peptide B	Rattus norvegicus	61-64
8027030-5	1994	Upon isolating and sequencing 2.5 kilobases of the rat BNP 5"-flanking sequence (FS), a variety of putative transcriptional enhancer sites were identified, including several GATA consensus sequences (WGATAR), one of which apparently serves as the major promoter site.	gata	174-178	natriuretic peptide B	Rattus norvegicus	55-58
8027030-7	1994	Truncation analyses showed that inducibility mapped primarily to the proximal -116 base pair of the rat BNP 5"-FS, where there are two consensus GATA sites in addition to the GATA sequence at the TATA box.	gata	145-149	natriuretic peptide B	Rattus norvegicus	104-107
8027030-7	1994	Truncation analyses showed that inducibility mapped primarily to the proximal -116 base pair of the rat BNP 5"-FS, where there are two consensus GATA sites in addition to the GATA sequence at the TATA box.	gata	175-179	natriuretic peptide B	Rattus norvegicus	104-107
8027030-8	1994	Point mutation analyses showed that at least one of the GATA sites was required to confer full GATA-4-inducible transcription.	gata	56-60	GATA binding protein 4	Rattus norvegicus	95-101
8027030-9	1994	These results demonstrate that a proximal region of the rat BNP 5"-FS is required for growth factor- and GATA-inducible transcription, supporting the view that the BNP gene could serve as a target for GATA-binding proteins during early cardiac development.	gata	105-109	natriuretic peptide B	Rattus norvegicus	60-63
8027030-9	1994	These results demonstrate that a proximal region of the rat BNP 5"-FS is required for growth factor- and GATA-inducible transcription, supporting the view that the BNP gene could serve as a target for GATA-binding proteins during early cardiac development.	gata	105-109	natriuretic peptide B	Rattus norvegicus	164-167
8027030-9	1994	These results demonstrate that a proximal region of the rat BNP 5"-FS is required for growth factor- and GATA-inducible transcription, supporting the view that the BNP gene could serve as a target for GATA-binding proteins during early cardiac development.	gata	201-205	natriuretic peptide B	Rattus norvegicus	60-63
8027030-9	1994	These results demonstrate that a proximal region of the rat BNP 5"-FS is required for growth factor- and GATA-inducible transcription, supporting the view that the BNP gene could serve as a target for GATA-binding proteins during early cardiac development.	gata	201-205	myotrophin	Rattus norvegicus	86-99
8027030-9	1994	These results demonstrate that a proximal region of the rat BNP 5"-FS is required for growth factor- and GATA-inducible transcription, supporting the view that the BNP gene could serve as a target for GATA-binding proteins during early cardiac development.	gata	201-205	natriuretic peptide B	Rattus norvegicus	164-167
8150083-3	1994	These complexes bind to GATA motifs of the rho-globin promoter and histone H5 enhancer with high affinity, and to the chicken beta-globin promoter specialized TATA element and enhancer GATA with low affinity.	gata	24-28	hemoglobin beta, subunit rho	Gallus gallus	43-53
8150083-3	1994	These complexes bind to GATA motifs of the rho-globin promoter and histone H5 enhancer with high affinity, and to the chicken beta-globin promoter specialized TATA element and enhancer GATA with low affinity.	gata	185-189	hemoglobin beta, subunit rho	Gallus gallus	43-53
8370527-5	1993	We find that TBP (TATA-binding protein) alone can activate transcription of beta-globin chromatin templates from promoters mutated to a canonical TATA box but is ineffective on those containing the normal -30 GATA site.	gata	209-213	TATA-box binding protein	Gallus gallus	13-16
8449904-9	1993	Mutations and deletions of both sites indicate that only the association of CCACC/Sp1 and GATA binding sites can drive efficient and tissue-specific expression of this R-PK minimal promoter.	gata	90-94	pyruvate kinase L/R	Homo sapiens	168-172
8370527-5	1993	We find that TBP (TATA-binding protein) alone can activate transcription of beta-globin chromatin templates from promoters mutated to a canonical TATA box but is ineffective on those containing the normal -30 GATA site.	gata	209-213	TATA-box binding protein	Gallus gallus	18-38
1744088-4	1991	In all three mast cell lines, the promoter activity of the MC-CPA gene depended on the GATA binding site.	gata	87-91	carboxypeptidase A3	Homo sapiens	59-65
1596565-13	1992	Inspection of the 5" flanking region of the TFPI gene showed a conserved GATA-binding motif located approximately 400 bp upstream of the proposed transcription initiation site(s).	gata	73-77	tissue factor pathway inhibitor	Homo sapiens	44-48
1583720-0	1992	Differential factor binding at the promoter of early baculovirus gene PE38 during viral infection: GATA motif is recognized by an insect protein.	gata	99-103	hypothetical protein	Autographa californica nucleopolyhedrovirus	70-74
1583720-2	1992	A GATA motif located 50 nucleotides upstream of the PE38 transcriptional start site is recognized differentially in the course of infection.	gata	2-6	hypothetical protein	Autographa californica nucleopolyhedrovirus	52-56
7678994-5	1993	In addition, our results indicate that the tal-1 1A promoter, which contains two consensus GATA-binding sites, is active mainly in these lineages.	gata	91-95	TAL bHLH transcription factor 1, erythroid differentiation factor	Homo sapiens	43-48
1396592-3	1992	We used gel shift and transfection assays to demonstrate that the GATA motif in the SCL promoter binds GATA-1 (and GATA-2), and also mediates transcriptional transactivation.	gata	66-70	GATA binding protein 1	Homo sapiens	103-109
1396592-3	1992	We used gel shift and transfection assays to demonstrate that the GATA motif in the SCL promoter binds GATA-1 (and GATA-2), and also mediates transcriptional transactivation.	gata	66-70	GATA binding protein 2	Homo sapiens	115-121
1590778-6	1992	Gel-mobility-shift assays with 23 bp oligonucleotides containing the GATA-binding site (AGATAA) of the histone H5 enhancer or of the beta-globin enhancer showed that the GATA sequence was sufficient for the formation of at least five complexes.	gata	69-73	H1 histone family, member 0	Gallus gallus	103-113
1590778-6	1992	Gel-mobility-shift assays with 23 bp oligonucleotides containing the GATA-binding site (AGATAA) of the histone H5 enhancer or of the beta-globin enhancer showed that the GATA sequence was sufficient for the formation of at least five complexes.	gata	89-93	H1 histone family, member 0	Gallus gallus	103-113
1918021-6	1991	A nuclear protein binding to the GATA motif in Region A has been identified and proven to be necessary for expression of the ET1 gene.	gata	33-37	endothelin 1	Homo sapiens	125-128
1944279-8	1991	On the basis of the above-described results, we propose that the megakaryocyte-specific enhancer/silencer domain and the GATA site are responsible for high-level expression of the PF4 gene in a lineage-specific manner.	gata	121-125	platelet factor 4	Rattus norvegicus	180-183
1766438-7	1991	Characteristic GATA repeats with a conserved spacing were found in 5" upstream sequences of cab 1A-D, cab 3A-C, cab 11 and cab 12.	gata	15-19	chlorophyll a/b-binding protein Cab-1A	Solanum lycopersicum	92-98
1766438-7	1991	Characteristic GATA repeats with a conserved spacing were found in 5" upstream sequences of cab 1A-D, cab 3A-C, cab 11 and cab 12.	gata	15-19	chlorophyll a-b binding protein CAB11	Solanum lycopersicum	112-118
2044960-6	1991	Full promoter activity requires the presence of proximal CACCC box sequences and an upstream, double GATA motif that binds a single GATA-1 molecule in an asymmetric fashion.	gata	101-105	GATA binding protein 1	Mus musculus	132-138
2388628-6	1990	Gel shift analysis, methylation interference, protein-DNA cross-linking, and oligonucleotide competition studies revealed that BAE cell nuclear extract contains a 47-kilodalton DNA-binding protein recognizing the core motif TATC (GATA) located at positions -135 to -132 of the PPET-1 promoter.	gata	230-234	zinc finger protein 763	Homo sapiens	177-196
2388628-6	1990	Gel shift analysis, methylation interference, protein-DNA cross-linking, and oligonucleotide competition studies revealed that BAE cell nuclear extract contains a 47-kilodalton DNA-binding protein recognizing the core motif TATC (GATA) located at positions -135 to -132 of the PPET-1 promoter.	gata	230-234	endothelin 1	Bos taurus	277-283
2388628-11	1990	We conclude that a nuclear factor with binding specificity for a GATA motif similar to that of the transcriptional activator GF-1 is necessary for the efficient and cell-specific expression of the human PPET-1 gene.	gata	65-69	GATA binding protein 1	Homo sapiens	125-129
2388628-11	1990	We conclude that a nuclear factor with binding specificity for a GATA motif similar to that of the transcriptional activator GF-1 is necessary for the efficient and cell-specific expression of the human PPET-1 gene.	gata	65-69	endothelin 1	Homo sapiens	203-209
1827068-5	1991	hGATA-3 contains a zinc finger domain that is highly related to the DNA-binding domain of the erythroid-specific transcription factor, GATA-1, and binds to a region of T alpha 3 that contains a consensus GATA binding site (AGATAG).	gata	1-5	GATA binding protein 1	Homo sapiens	135-141
2276623-1	1990	The murine, erythroid DNA-binding protein GF-1 (also known as NF-E1, Eryf 1), a 413-amino acid polypeptide with two novel finger domains of the Cx-Cx variety, recognizes a consensus GATA motif present in cis elements of the majority of erythroid-expressed genes.	gata	182-186	gonadal fat pad weight 1	Mus musculus	42-46
2276623-1	1990	The murine, erythroid DNA-binding protein GF-1 (also known as NF-E1, Eryf 1), a 413-amino acid polypeptide with two novel finger domains of the Cx-Cx variety, recognizes a consensus GATA motif present in cis elements of the majority of erythroid-expressed genes.	gata	182-186	YY1 transcription factor	Mus musculus	62-67
2276623-1	1990	The murine, erythroid DNA-binding protein GF-1 (also known as NF-E1, Eryf 1), a 413-amino acid polypeptide with two novel finger domains of the Cx-Cx variety, recognizes a consensus GATA motif present in cis elements of the majority of erythroid-expressed genes.	gata	182-186	GATA binding protein 1	Mus musculus	69-75
2276623-3	1990	Using a cotransfection assay, we find that GF-1 is a potent transcriptional activator with several activation domains but that this is revealed only in heterologous cells and with reporters containing minimal promoters onto which either a single or multiple GATA-binding sites are placed.	gata	258-262	gonadal fat pad weight 1	Mus musculus	43-47
2276623-6	1990	The role of each finger is more pronounced with some GATA-binding sites than with others, suggesting a diversity of interactions between GF-1 and different target sites.	gata	53-57	gonadal fat pad weight 1	Mus musculus	137-141
34897794-5	2022	This study expands the spectrum of genetic defects associated with BDE2 and TRPS and demonstrates the pathogenicity of TRPS1 missense variants located outside both the nuclear localization signal and the GATA and Ikaros-like binding domains.	gata	204-208	transcriptional repressor GATA binding 1	Homo sapiens	119-124