PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 9038161-9 1997 A consensus element with homology to the URS sequence of the ENO1 promoter was found in the promoters of the GPD1, GPP2, GCY1, and DAK1 genes. Peptichemio 41-44 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 61-65 7502579-1 1995 The activity of an upstream repression sequence (URS element) that mediates a 20-fold repression of ENO1 expression in cells grown in a medium containing glucose was characterized. Peptichemio 49-52 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 100-104 7502579-2 1995 Sequences that are sufficient for orientation-dependent ENO1 URS element activity were mapped between positions -241 and -126 relative to the ENO1 transcriptional initiation site. Peptichemio 61-64 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 56-60 7502579-2 1995 Sequences that are sufficient for orientation-dependent ENO1 URS element activity were mapped between positions -241 and -126 relative to the ENO1 transcriptional initiation site. Peptichemio 61-64 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 142-146 7502579-3 1995 The ENO1 URS element repressed transcription of the yeast CYC1 gene when positioned between the CYC1 upstream activation sequences (UAS elements) and TATAAA boxes. Peptichemio 9-12 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 4-8 7502579-4 1995 The ENO1 URS element failed to repress transcription of the wild-type yeast enolase gene ENO2; however, expression of an ENO2 gene lacking one of the ENO2 UAS elements was efficiently repressed by the ENO1 URS element, suggesting that the URS element interferes with the transcriptional activation by some, but not all, UAS elements. Peptichemio 9-12 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 4-8 7502579-4 1995 The ENO1 URS element failed to repress transcription of the wild-type yeast enolase gene ENO2; however, expression of an ENO2 gene lacking one of the ENO2 UAS elements was efficiently repressed by the ENO1 URS element, suggesting that the URS element interferes with the transcriptional activation by some, but not all, UAS elements. Peptichemio 206-209 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 4-8 7502579-4 1995 The ENO1 URS element failed to repress transcription of the wild-type yeast enolase gene ENO2; however, expression of an ENO2 gene lacking one of the ENO2 UAS elements was efficiently repressed by the ENO1 URS element, suggesting that the URS element interferes with the transcriptional activation by some, but not all, UAS elements. Peptichemio 206-209 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 201-205 7502579-4 1995 The ENO1 URS element failed to repress transcription of the wild-type yeast enolase gene ENO2; however, expression of an ENO2 gene lacking one of the ENO2 UAS elements was efficiently repressed by the ENO1 URS element, suggesting that the URS element interferes with the transcriptional activation by some, but not all, UAS elements. Peptichemio 206-209 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 4-8 7502579-4 1995 The ENO1 URS element failed to repress transcription of the wild-type yeast enolase gene ENO2; however, expression of an ENO2 gene lacking one of the ENO2 UAS elements was efficiently repressed by the ENO1 URS element, suggesting that the URS element interferes with the transcriptional activation by some, but not all, UAS elements. Peptichemio 206-209 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 201-205 7502579-5 1995 In contrast to the ENO1 gene, the ENO1 URS element repressed CYC1 and ENO2 expression in cells grown on glucose or glycerol plus lactate. Peptichemio 39-42 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 34-38 7502579-6 1995 Evidence is presented that the ENO1 URS element also functions during stationary growth phase. Peptichemio 36-39 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 31-35 8144571-1 1994 Cis-acting sequences that modulate ENO1 URS (upstream repression site) element activity were identified by base pair substitution mutagenesis. Peptichemio 40-43 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 35-39 8144571-4 1994 A binding site for the yeast REB1 protein was identified near the 5" terminus of the ENO1 URS element. Peptichemio 90-93 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 85-89 8144571-8 1994 Base substitution mutations within a second region of the ENO1 URS element caused a 38% loss of URS activity in vivo. Peptichemio 63-66 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 58-62 8144571-8 1994 Base substitution mutations within a second region of the ENO1 URS element caused a 38% loss of URS activity in vivo. Peptichemio 96-99 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 58-62 8144571-10 1994 Base substitution mutations within a third region near the 3" terminus of the ENO1 URS element caused a 70% loss of URS activity in vivo. Peptichemio 83-86 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 78-82 8144571-10 1994 Base substitution mutations within a third region near the 3" terminus of the ENO1 URS element caused a 70% loss of URS activity in vivo. Peptichemio 116-119 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 78-82 8144571-12 1994 These results showed that ENO1 URS element activity was modulated by multiple cis-acting sequences that bound distinct trans-acting factors. Peptichemio 31-34 phosphopyruvate hydratase ENO1 Saccharomyces cerevisiae S288C 26-30