Longo Valter D
Andrus Gerontology Center and Department of Biological Sciences, University of Southern California, Los Angeles, CA 90089, USA.
Sci Aging Knowledge Environ. 2004 Sep 29;2004(39):pe36. doi: 10.1126/sageke.2004.39.pe36.
Studies in worms, flies, and mice point to the insulin/insulin-like growth factor-1 (IGF-1)/phosphatidylinositol 3-kinase/Akt-like pathway as a central regulator of longevity. A similar pathway, which includes Sch9, a functional mammalian Akt/protein kinase B homolog, regulates longevity in yeast. Chronological aging in yeast is also regulated by a second pathway that includes Ras, adenylate cyclase, protein kinase A, the transcription factors Msn2 and Msn4, and Sod2. Although Ras proteins have not been implicated in longevity regulation in worms or flies, the major role of Ras in mammalian IGF-1 signaling raises the possibility that homologs of yeast Ras2 might accelerate aging in mammals. Here I review the data from experiments at both the organismal and cellular levels that support a role for Ras in the regulation of stress resistance and life span in eukaryotes.
对蠕虫、果蝇和小鼠的研究表明,胰岛素/胰岛素样生长因子-1(IGF-1)/磷脂酰肌醇3-激酶/Akt样信号通路是寿命的核心调节因子。在酵母中,一条类似的信号通路(包括功能性哺乳动物Akt/蛋白激酶B同源物Sch9)调节寿命。酵母中的时序衰老还受另一条信号通路的调节,该通路包括Ras、腺苷酸环化酶、蛋白激酶A、转录因子Msn2和Msn4以及Sod2。尽管尚未发现Ras蛋白与蠕虫或果蝇的寿命调节有关,但Ras在哺乳动物IGF-1信号传导中的主要作用增加了酵母Ras2同源物可能加速哺乳动物衰老的可能性。在此,我回顾了来自生物体和细胞水平实验的数据,这些数据支持Ras在真核生物应激抗性和寿命调节中的作用。