Negative control of p53 by Sir2alpha promotes cell survival under stress

Cell. 2001 Oct 19;107(2):137-48. doi: 10.1016/s0092-8674(01)00524-4.

Abstract

The NAD-dependent histone deacetylation of Sir2 connects cellular metabolism with gene silencing as well as aging in yeast. Here, we show that mammalian Sir2alpha physically interacts with p53 and attenuates p53-mediated functions. Nicotinamide (Vitamin B3) inhibits an NAD-dependent p53 deacetylation induced by Sir2alpha, and also enhances the p53 acetylation levels in vivo. Furthermore, Sir2alpha represses p53-dependent apoptosis in response to DNA damage and oxidative stress, whereas expression of a Sir2alpha point mutant increases the sensitivity of cells in the stress response. Thus, our findings implicate a p53 regulatory pathway mediated by mammalian Sir2alpha. These results have significant implications regarding an important role for Sir2alpha in modulating the sensitivity of cells in p53-dependent apoptotic response and the possible effect in cancer therapy.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Apoptosis
  • Blotting, Western
  • Cell Death
  • Cell Line
  • Cell Survival
  • DNA Damage
  • DNA, Complementary / metabolism
  • Dose-Response Relationship, Drug
  • Electrophoresis, Polyacrylamide Gel
  • Histone Deacetylases / metabolism*
  • Humans
  • Mice
  • Mutagenesis, Site-Directed
  • NAD / metabolism
  • Neoplasms / metabolism
  • Neoplasms / therapy
  • Niacinamide / pharmacology
  • Oxidative Stress*
  • Point Mutation
  • Poly(ADP-ribose) Polymerases / metabolism
  • Polymerase Chain Reaction
  • Protein Binding
  • Protein Structure, Tertiary
  • Sirtuin 1
  • Sirtuins / metabolism*
  • Trans-Activators / metabolism*
  • Transcriptional Activation
  • Tumor Suppressor Protein p53 / biosynthesis*
  • fas Receptor / metabolism

Substances

  • DNA, Complementary
  • Trans-Activators
  • Tumor Suppressor Protein p53
  • fas Receptor
  • NAD
  • Niacinamide
  • Poly(ADP-ribose) Polymerases
  • SIRT1 protein, human
  • Sirt1 protein, mouse
  • Sirtuin 1
  • Sirtuins
  • Histone Deacetylases