The molecular biology of mammalian SIRT proteins: SIRT2 in cell cycle regulation

Cell Cycle. 2007 May 2;6(9):1011-8. doi: 10.4161/cc.6.9.4219. Epub 2007 May 30.

Abstract

Sir2, an NAD+-dependent protein deacetylase, extends the lifespan in diverse species from yeast to flies. Mammals have seven homologs of Sir2, SIRT1-7, which affect aging and metabolism and which are potential targets for pharmacologic intervention. We identified SIRT2, which preferentially deacetylates tubulin and histone H4, as a downregulated protein in gliomas due to its epigenetic aberration. We herein discuss the role of SIRT2 in the mitotic checkpoint function and show that it may be as a potential target of anti-cancer drugs.

Publication types

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

MeSH terms

  • Aneuploidy
  • Animals
  • Cell Cycle / physiology*
  • Histone Deacetylases / genetics
  • Histone Deacetylases / metabolism
  • Histones / metabolism
  • Humans
  • Mice
  • Mitosis
  • Models, Biological
  • Neoplasms / drug therapy
  • Neoplasms / metabolism
  • Polyploidy
  • Silent Information Regulator Proteins, Saccharomyces cerevisiae / genetics
  • Silent Information Regulator Proteins, Saccharomyces cerevisiae / metabolism
  • Sirtuin 2
  • Sirtuins / genetics
  • Sirtuins / metabolism
  • Sirtuins / physiology*
  • Tubulin / metabolism

Substances

  • Histones
  • Silent Information Regulator Proteins, Saccharomyces cerevisiae
  • Tubulin
  • SIR2 protein, S cerevisiae
  • Sirtuin 2
  • Sirtuins
  • Histone Deacetylases