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

被引:0
|
作者
Siu Sylvia Lee
Raymond Y.N. Lee
Andrew G. Fraser
Ravi S. Kamath
Julie Ahringer
Gary Ruvkun
机构
[1] Harvard Medical School,Department of Molecular Biology, Massachusetts General Hospital and Department of Genetics
[2] Wellcome Trust/Cancer Research UK Institute,WormBase, Division of Biology
[3] University of Cambridge,undefined
[4] California Institute of Technology,undefined
来源
Nature Genetics | 2003年 / 33卷
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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.
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页码:40 / 48
页数:8
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