Longo Valter D, Fabrizio Paola
Department of Biological Sciences, Andrus Gerontology Center, University of Southern California, Los Angeles, CA, 90089-0191, USA,
Subcell Biochem. 2012;57:101-21. doi: 10.1007/978-94-007-2561-4_5.
The two paradigms to study aging in Saccharomyces cerevisiae are the chronological life span (CLS) and the replicative life span (RLS). The chronological life span is a measure of the mean and maximum survival time of non-dividing yeast populations while the replicative life span is based on the mean and maximum number of daughter cells generated by an individual mother cell before cell division stops irreversibly. Here we review the principal discoveries associated with yeast chronological aging and how they are contributing to the understanding of the aging process and of the molecular mechanisms that may lead to healthy aging in mammals. We will focus on the mechanisms of life span regulation by the Tor/Sch9 and the Ras/adenylate Ras/adenylate cyclase/PKA pathways with particular emphasis on those implicating age-dependent oxidative oxidative stress stress and DNA damage/repair.
在酿酒酵母中研究衰老的两种范式是时序寿命(CLS)和复制寿命(RLS)。时序寿命是衡量不分裂酵母群体平均和最长存活时间的指标,而复制寿命则基于单个母细胞在细胞分裂不可逆停止前产生的子细胞的平均和最大数量。在这里,我们回顾与酵母时序衰老相关的主要发现,以及它们如何有助于理解衰老过程和可能导致哺乳动物健康衰老的分子机制。我们将重点关注Tor/Sch9和Ras/腺苷酸环化酶/PKA途径对寿命的调节机制,特别强调那些涉及年龄依赖性氧化应激和DNA损伤/修复的机制。