Giannakou Maria E, Goss Martin, Partridge Linda
Centre for Research on Aging, Department of Biology, University College London, Darwin Building, Gower Street, London WC1E 6BT, UK.
Aging Cell. 2008 Mar;7(2):187-98. doi: 10.1111/j.1474-9726.2007.00362.x. Epub 2008 Jan 30.
Dietary restriction (DR) increases lifespan in diverse organisms. However, the mechanisms by which DR increases survival are unclear. The insulin/IGF-like signaling (IIS) pathway has been implicated in the response to DR in some studies, while in others it has appeared to play little or no role. We used the fruitfly Drosophila melanogaster to investigate the responses to DR of flies mutant for the transcription factor dFOXO, the main transcription factor target of IIS. We found that lifespan extension by DR does not require dFOXO. However, flies with dFOXO overexpressed in the adult fat body showed an altered response to DR and behaved as though partially dietarily restricted. These results suggest that, although DR extends lifespan of flies in the absence of dFOXO, the presence of active dFOXO modulates the response to DR, possibly by modifying expression of its target genes, and may therefore mediate the normal response to DR.
饮食限制(DR)可延长多种生物的寿命。然而,DR 增加存活率的机制尚不清楚。在一些研究中,胰岛素/胰岛素样生长因子信号(IIS)通路与对 DR 的反应有关,而在另一些研究中,它似乎作用很小或没有作用。我们使用果蝇 Drosophila melanogaster 来研究转录因子 dFOXO(IIS 的主要转录因子靶点)突变的果蝇对 DR 的反应。我们发现 DR 延长寿命并不需要 dFOXO。然而,在成年脂肪体中过表达 dFOXO 的果蝇对 DR 的反应发生了改变,表现得好像部分受到了饮食限制。这些结果表明,尽管在没有 dFOXO 的情况下 DR 可延长果蝇寿命,但活跃的 dFOXO 的存在可能通过修饰其靶基因的表达来调节对 DR 的反应,因此可能介导对 DR 的正常反应。