Department of Anatomy and Cell Biology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.
Int J Mol Sci. 2018 Jun 27;19(7):1888. doi: 10.3390/ijms19071888.
In aging cells, genomic instability is now recognized as a hallmark event. Throughout life, cells encounter multiple endogenous and exogenous DNA damaging events that are mostly repaired, but inevitably DNA mutations, chromosome rearrangements, and epigenetic deregulation begins to mount. Now that people are living longer, more and more late life time is spent suffering from age-related disease, in which genomic instability plays a critical role. However, several major questions remain heavily debated, such as the following: When does aging start? How long can we live? In order to minimize the impact of genomic instability on longevity, it is important to understand when aging starts, and to ensure repair mechanisms remain optimal from the very start to the very end. In this review, the interplay between the stress and nutrient response networks, and the regulation of homeostasis and genomic stability, is discussed. Mechanisms that link these two networks are predicted to be key lifespan determinants. The Anaphase Promoting Complex (APC), a large evolutionarily conserved ubiquitin ligase, can potentially serve this need. Recent work demonstrates that the APC maintains genomic stability, mounts a stress response, and increases longevity in yeast. Furthermore, inhibition of APC activity by glucose and nutrient response factors indicates a tight link between the APC and the stress/nutrient response networks.
在衰老细胞中,基因组不稳定性现在被认为是一个标志性事件。在整个生命过程中,细胞会遇到多种内源性和外源性的 DNA 损伤事件,这些事件大部分都可以被修复,但不可避免的是,DNA 突变、染色体重排和表观遗传失调开始累积。现在人们的寿命越来越长,越来越多的人在晚年遭受与年龄相关的疾病,其中基因组不稳定性起着关键作用。然而,仍有几个重大问题备受争议,例如:衰老何时开始?我们能活多久?为了将基因组不稳定性对寿命的影响降到最低,了解衰老何时开始以及确保修复机制从一开始就保持最佳状态至关重要。在这篇综述中,讨论了应激和营养响应网络之间的相互作用,以及体内平衡和基因组稳定性的调节。预测将这两个网络联系起来的机制将是关键的寿命决定因素。有丝分裂促进复合物(APC)是一种大型的进化上保守的泛素连接酶,它可能满足这一需求。最近的研究表明,APC 维持基因组稳定性、引发应激反应并延长酵母的寿命。此外,葡萄糖和营养响应因子对 APC 活性的抑制表明 APC 与应激/营养响应网络之间存在紧密联系。