A nicotinamide phosphoribosyltransferase-GAPDH interaction sustains the stress-induced NMN/NAD⁺ salvage pathway in the nucleus.

ABSTRACT: All cells require sustained intracellular energy flux, which is driven by redox chemistry at the subcellular level. NAD⁺, its phosphorylated variant NAD(P)⁺, and its reduced forms NAD(P)/NAD(P)H are all redox cofactors with key roles in energy metabolism and are substrates for several NAD-consuming enzymes (e.g. poly(ADP-ribose) polymerases, sirtuins, and others). The nicotinamide salvage pathway, constituted by nicotinamide mononucleotide adenylyltransferase (NMNAT) and nicotinamide phosphoribosyltransferase (NAMPT), mainly replenishes NAD⁺ in eukaryotes. However, unlike NMNAT1, NAMPT is not known to be a nuclear protein, prompting the question of how the nuclear NAD⁺ pool is maintained and how it is replenished upon NAD⁺ consu

SUBMITTER: Grolla AA 

PROVIDER: S-EPMC7076215 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature