HST2 mediates SIR2-independent life-span extension by catorie restriction

被引:174
作者
Lamming, DW
Latorre-Esteves, M
Medvedik, O
Wong, SN
Tsang, FA
Wang, C
Lin, SJ
Sinclair, DA
机构
[1] Harvard Univ, Sch Med, Dept Pathol, Paul F Glenn Labs Biol Mech Aging, Boston, MA 02115 USA
[2] Univ Calif Davis, Ctr Genet & Dev, Davis, CA 95616 USA
[3] Univ Calif Davis, Microbiol Sect, Davis, CA 95616 USA
关键词
D O I
10.1126/science.1113611
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Calorie restriction (CR) extends the life span of numerous species, from yeast to rodents. Yeast Sir2 is a nicotinamide adenine dinucleotide (NAD+)dependent histone deacetylase that has been proposed to mediate the effects of CR. However, this hypothesis has been challenged by the observation that CR can extend yeast life span in the absence of Sir2. Here, we show that Sir2-independent life-span extension is mediated by Hst2, a Sir2 homolog that promotes the stability of repetitive ribosomal DNA, the same mechanism by which Sir2 extends life span. These findings demonstrate that the maintenance of DNA stability is critical for yeast life-span extension by CR and suggest that, in higher organisms, multiple members of the Sir2 family may regulate life span in response to diet.
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收藏
页码:1861 / 1864
页数:4
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