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一项功能获得性筛选鉴定出 wdb 和 lkb1 是果蝇寿命延长的基因。

A gain-of-function screen identifies wdb and lkb1 as lifespan-extending genes in Drosophila.

机构信息

Department of Biological Sciences, Tokyo Metropolitan University, 1-1 Minami-osawa, Hachioji, Tokyo 192-0397, Japan.

出版信息

Biochem Biophys Res Commun. 2011 Feb 25;405(4):667-72. doi: 10.1016/j.bbrc.2011.01.090. Epub 2011 Jan 31.

Abstract

The insulin/insulin-like growth factor (IGF) and the target of rapamycin (TOR) signaling pathways are known to regulate lifespan in diverse organisms. However, only a limited number of genes involved in these pathways have been examined regarding their effects on lifespan. Through a gain-of-function screen in Drosophila, we found that overexpression of the wdb gene encoding a regulatory subunit of PP2A, and overexpression of the lkb1 gene encoding a serine/threonine kinase, reduced organ size and extended lifespan. Overexpression of wdb also reduced the level of phosphorylated AKT, while overexpression of lkb1 increased the level of phosphorylated AMPK and decreased the level of phosphorylated S6K. Taken together, our results suggest that wdb- and lkb1-dependent lifespan extension is mediated by downregulation of S6K, a downstream component of the insulin/IGF and TOR signaling pathways.

摘要

胰岛素/胰岛素样生长因子 (IGF) 和雷帕霉素靶蛋白 (TOR) 信号通路已知可调节不同生物的寿命。然而,关于这些通路中哪些基因参与调节寿命,目前仅对少数基因进行了研究。通过在果蝇中进行功能获得性筛选,我们发现,编码 PP2A 调节亚基的 wdb 基因和编码丝氨酸/苏氨酸激酶的 lkb1 基因的过表达会减小器官大小并延长寿命。wdb 的过表达还降低了磷酸化 AKT 的水平,而 lkb1 的过表达则增加了磷酸化 AMPK 的水平并降低了磷酸化 S6K 的水平。综上所述,我们的结果表明,wdb 和 lkb1 依赖的寿命延长是通过下调 S6K 介导的,S6K 是胰岛素/IGF 和 TOR 信号通路的下游成分。

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