Guest guest Posted July 7, 2005 Report Share Posted July 7, 2005 Just an interesting find. Apparently there are 89 genes that when " interfered " with in C. elegans, produce lifespan extension. What is particularly interesting is that many of the genes in question have human homologs. Many of the genes, however, are " upstream " and " downstream " from the relatively well-characterized " insulin/IGF-I " pathway, so it may be that there is a little bit of redundancy. But, the authors are convinced that some of the genes they found are operating independently of the previously characterized genes. I guess the only caveat here is that worms are a long way from humans... =--==-=-=-=-- Genes Dev. 2005 Jul 1;19(13):1544-55. Related Articles, Links A systematic RNAi screen for longevity genes in C. elegans. Hamilton B, Dong Y, Shindo M, Liu W, Odell I, Ruvkun G, Lee SS. We report here the first genome-wide functional genomic screen for longevity genes. We systematically surveyed Caenorhabditis elegans genes using large-scale RNA interference (RNAi), and found that RNAi inactivation of 89 genes extend C. elegans lifespan. Components of the daf-2/insulin-like signaling pathway are recovered, as well as genes that regulate metabolism, signal transduction, protein turnover, and gene expression. Many of these candidate longevity genes are conserved across animal phylogeny. Genetic interaction analyses with the new longevity genes indicate that some act upstream of the daf-16/FOXO transcription factor or the sir2.1 protein deacetylase, and others function independently of daf-16/FOXO and sir2.1, and might define new pathways to regulate lifespan. PMID: 15998808 [PubMed - in process] =-=-=-===--== T. pct35768@... Quote Link to comment Share on other sites More sharing options...
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