p66Shc:: at the crossroad of oxidative stress and the genetics of aging

被引:55
|
作者
Purdom, S
Chen, QM
机构
[1] Univ Arizona, Dept Pharmacol, Tucson, AZ 85724 USA
[2] Univ Arizona, Interdisciplinary Grad Program Genet & Genom, Tucson, AZ 85724 USA
关键词
D O I
10.1016/S1471-4914(03)00048-0
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
The biology of aging has been mysterious for centuries. Removal of the p66(Shc) gene, which encodes an adaptor protein for cell signaling, extends lifespan by -30% in mice and confers resistance to oxidative stress. The absence of p66(Shc) correlates with reduced levels of apoptosis. Oxidants induce phosphorylation of serine36 on P66(Shc), contributing to inactivation of members of the Forkhead transcription factor family, some of which appear to regulate the expression of antioxidant genes. The expression of p66(Shc) is regulated by the methylation status of its promoter. This leads us to hypothesize that increased methylation of the p66(Shc) promoter might contribute to the absence of its expression and therefore extended longevity in particular individuals.
引用
收藏
页码:206 / 210
页数:5
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