Murphy Coleen T, McCarroll Steven A, Bargmann Cornelia I, Fraser Andrew, Kamath Ravi S, Ahringer Julie, Li Hao, Kenyon Cynthia
Department of Biochemistry and Biophysics, University of California, San Francisco, California 94143-2200, USA.
Nature. 2003 Jul 17;424(6946):277-83. doi: 10.1038/nature01789. Epub 2003 Jun 29.
Ageing is a fundamental, unsolved mystery in biology. DAF-16, a FOXO-family transcription factor, influences the rate of ageing of Caenorhabditis elegans in response to insulin/insulin-like growth factor 1 (IGF-I) signalling. Using DNA microarray analysis, we have found that DAF-16 affects expression of a set of genes during early adulthood, the time at which this pathway is known to control ageing. Here we find that many of these genes influence the ageing process. The insulin/IGF-I pathway functions cell non-autonomously to regulate lifespan, and our findings suggest that it signals other cells, at least in part, by feedback regulation of an insulin/IGF-I homologue. Furthermore, our findings suggest that the insulin/IGF-I pathway ultimately exerts its effect on lifespan by upregulating a wide variety of genes, including cellular stress-response, antimicrobial and metabolic genes, and by downregulating specific life-shortening genes.
衰老在生物学领域是一个根本的、尚未解决的谜团。DAF-16是一种FOXO家族转录因子,它能响应胰岛素/胰岛素样生长因子1(IGF-I)信号通路,影响秀丽隐杆线虫的衰老速率。通过DNA微阵列分析,我们发现DAF-16在成年早期会影响一组基因的表达,而这一时期正是已知该信号通路控制衰老的时间。在此我们发现,这些基因中的许多都对衰老过程有影响。胰岛素/IGF-I信号通路通过非细胞自主方式发挥作用来调节寿命,我们的研究结果表明,它至少部分地通过对胰岛素/IGF-I同源物的反馈调节向其他细胞发出信号。此外,我们的研究结果表明,胰岛素/IGF-I信号通路最终通过上调包括细胞应激反应、抗菌和代谢基因在内的多种基因,以及下调特定的缩短寿命的基因,来对寿命产生影响。