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Sir2通过与热量限制相关的途径介导果蝇的长寿。

Sir2 mediates longevity in the fly through a pathway related to calorie restriction.

作者信息

Rogina Blanka, Helfand Stephen L

机构信息

Department of Genetics and Developmental Biology, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT 06030, USA.

出版信息

Proc Natl Acad Sci U S A. 2004 Nov 9;101(45):15998-6003. doi: 10.1073/pnas.0404184101. Epub 2004 Nov 1.

Abstract

Calorie restriction can extend life span in a variety of species including mammals, flies, nematodes, and yeast. Despite the importance of this nearly universal effect, little is understood about the molecular mechanisms that mediate the life-span-extending effect of calorie restriction in metazoans. Sir2 is known to be involved in life span determination and calorie restriction in yeast mother cells. In nematodes increased Sir2 can extend life span, but a direct link to calorie restriction has not been demonstrated. We now report that Sir2 is directly involved in the calorie-restriction life-span-extending pathway in Drosophila. We demonstrate that an increase in Drosophila Sir2 (dSir2) extends life span, whereas a decrease in dSir2 blocks the life-span-extending effect of calorie reduction or rpd3 mutations. These data lead us to propose a genetic pathway by which calorie restriction extends life span and provides a framework for genetic and pharmacological studies of life span extension in metazoans.

摘要

热量限制能够延长包括哺乳动物、果蝇、线虫和酵母在内的多种物种的寿命。尽管这种几乎普遍存在的效应很重要,但对于后生动物中介导热量限制延长寿命效应的分子机制却知之甚少。已知Sir2参与酵母母细胞的寿命决定和热量限制过程。在线虫中,增加Sir2可以延长寿命,但尚未证明其与热量限制有直接联系。我们现在报告,Sir2直接参与果蝇中热量限制延长寿命的途径。我们证明,果蝇Sir2(dSir2)的增加会延长寿命,而dSir2的减少则会阻断热量减少或rpd3突变的寿命延长效应。这些数据使我们提出了一个遗传途径,通过该途径热量限制可以延长寿命,并为后生动物寿命延长的遗传和药理学研究提供了一个框架。

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