Sir2 blocks extreme life-span extension

被引:323
作者
Fabrizio, P
Gattazzo, C
Battistella, L
Wei, M
Cheng, C
McGrew, K
Longo, VD
机构
[1] Univ So Calif, Andrus Gerontol Ctr, Los Angeles, CA 90089 USA
[2] Univ So Calif, Dept Biol Sci, Los Angeles, CA 90089 USA
[3] Univ So Calif, Mol & Computat Biol Dept, Los Angeles, CA 90089 USA
关键词
D O I
10.1016/j.cell.2005.08.042
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sir2 is a conserved deacetylase that modulates life span in yeast, worms, and files 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 sir2 Delta 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.
引用
收藏
页码:655 / 667
页数:13
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