The NAD Biosynthesis Pathway Mediated by Nicotinamide Phosphoribosyltransferase Regulates Sir2 Activity in Mammalian Cells
Washington University in St. Louis
Abstract
Recent studies have revealed new roles for NAD and its derivatives in transcriptional regulation. The evolutionarily conserved Sir2 protein family requires NAD for its deacetylase activity and regulates a variety of biological processes, such as stress response, differentiation, metabolism, and aging. Despite its absolute requirement for NAD, the regulation of Sir2 function by NAD biosynthesis pathways is poorly understood in mammals. In this study, we determined the kinetics of the NAD biosynthesis mediated by nicotinamide phosphoribosyltransferase (Nampt) and nicotinamide/nicotinic acid mononucleotide adenylyltransferase (Nmnat), and we examined its effects on the transcriptional regulatory function of the…
Citation impact
- FWCI
- 13.35
- Percentile
- 100%
- References
- 61
Authors
3Topics & keywords
- Nicotinamide phosphoribosyltransferase
- NAD+ kinase
- Biosynthesis
- Nicotinamide
- Phosphoribosyltransferase
- Chemistry
- Cell biology
- Biochemistry