A systematic RNAi screen identifies a critical role for mitochondria in C-elegans longevity

被引:719
作者
Lee, SS
Lee, RYN
Fraser, AG
Kamath, RS
Ahringer, J
Ruvkun, G [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Mol Biol, Boston, MA 02114 USA
[2] Harvard Univ, Dept Genet, Sch Med, Boston, MA 02114 USA
[3] Univ Cambridge, Wellcome Trust Canc Res UK Inst, Cambridge, England
基金
英国惠康基金;
关键词
D O I
10.1038/ng1056
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report a systematic RNA interference (RNAi) screen of 5,690 Caenorhabditis elegans genes for gene inactivations that increase lifespan. We found that genes important for mitochondrial function stand out as a principal group of genes affecting C. elegans lifespan. A classical genetic screen identified a mutation in the mitochondrial leucyl-tRNA synthetase gene (lrs-2) that impaired mitochondrial function and was associated with longer-lifespan. The long-lived worms with impaired mitochondria had lower ATP content and oxygen consumption, but differential responses to free-radical and other stresses. These data suggest that the longer lifespan of C. elegans with compromised mitochrondria cannot simply be assigned to lower free radical production and suggest a more complex coupling of metabolism and longevity.
引用
收藏
页码:40 / 48
页数:9
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