Sir2 blocks extreme life-span extension - PubMed (original) (raw)
. 2005 Nov 18;123(4):655-67.
doi: 10.1016/j.cell.2005.08.042.
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- PMID: 16286010
- DOI: 10.1016/j.cell.2005.08.042
Free article
Sir2 blocks extreme life-span extension
Paola Fabrizio et al. Cell. 2005.
Free article
Abstract
Sir2 is a conserved deacetylase that modulates life span in yeast, worms, and flies and stress response in mammals. In yeast, Sir2 is required for maintaining replicative life span, and increasing Sir2 dosage can delay replicative aging. We address the role of Sir2 in regulating chronological life span in yeast. Lack of Sir2 along with calorie restriction and/or mutations in the yeast AKT homolog, Sch9, or Ras pathways causes a dramatic chronological life-span extension. Inactivation of Sir2 causes uptake and catabolism of ethanol and upregulation of many stress-resistance and sporulation genes. These changes while sufficient to extend chronological life span in wild-type yeast require severe calorie restriction or additional mutations to extend life span of sir2Delta mutants. Our results demonstrate that effects of SIR2 on chronological life span are opposite to replicatve life span and suggest that the relevant activities of Sir2-like deacetylases may also be complex in higher eukaryotes.
Comment in
- The enigmatic role of Sir2 in aging.
Kennedy BK, Smith ED, Kaeberlein M. Kennedy BK, et al. Cell. 2005 Nov 18;123(4):548-50. doi: 10.1016/j.cell.2005.11.002. Cell. 2005. PMID: 16286003
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