Title : Enzymes in the NAD+ salvage pathway regulate SIRT1 activity at target gene promoters.

Pub. Date : 2009 Jul 24

PMID : 19478080






5 Functional Relationships(s)
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1 In mammals, nicotinamide phosphoribosyltransferase (NAMPT) and nicotinamide mononucleotide adenylyltransferase 1 (NMNAT-1) constitute a nuclear NAD(+) salvage pathway which regulates the functions of NAD(+)-dependent enzymes such as the protein deacetylase SIRT1. NAD nicotinamide nucleotide adenylyltransferase 1 Homo sapiens
2 In mammals, nicotinamide phosphoribosyltransferase (NAMPT) and nicotinamide mononucleotide adenylyltransferase 1 (NMNAT-1) constitute a nuclear NAD(+) salvage pathway which regulates the functions of NAD(+)-dependent enzymes such as the protein deacetylase SIRT1. NAD nicotinamide nucleotide adenylyltransferase 1 Homo sapiens
3 In mammals, nicotinamide phosphoribosyltransferase (NAMPT) and nicotinamide mononucleotide adenylyltransferase 1 (NMNAT-1) constitute a nuclear NAD(+) salvage pathway which regulates the functions of NAD(+)-dependent enzymes such as the protein deacetylase SIRT1. NAD nicotinamide nucleotide adenylyltransferase 1 Homo sapiens
4 In mammals, nicotinamide phosphoribosyltransferase (NAMPT) and nicotinamide mononucleotide adenylyltransferase 1 (NMNAT-1) constitute a nuclear NAD(+) salvage pathway which regulates the functions of NAD(+)-dependent enzymes such as the protein deacetylase SIRT1. NAD nicotinamide nucleotide adenylyltransferase 1 Homo sapiens
5 In this study we show that stable short hairpin RNA-mediated knockdown of NAMPT or NMNAT-1 in MCF-7 breast cancer cells reduces total cellular NAD(+) levels and alters global patterns of gene expression. NAD nicotinamide nucleotide adenylyltransferase 1 Homo sapiens