Gonzalo Susana
Radiation and Cancer Biology Division, Dept. of Radiation Oncology, Washington Univ. School of Medicine, 4511 Forest Park, St. Louis, MO 63108, USA.
J Appl Physiol (1985). 2010 Aug;109(2):586-97. doi: 10.1152/japplphysiol.00238.2010. Epub 2010 May 6.
Aging is a multifaceted process characterized by genetic and epigenetic changes in the genome. The genetic component of aging received initially all of the attention. Telomere attrition and accumulation of mutations due to a progressive deficiency in the repair of DNA damage with age remain leading causes of genomic instability. However, epigenetic mechanisms have now emerged as key contributors to the alterations of genome structure and function that accompany aging. The three pillars of epigenetic regulation are DNA methylation, histone modifications, and noncoding RNA species. Alterations of these epigenetic mechanisms affect the vast majority of nuclear processes, including gene transcription and silencing, DNA replication and repair, cell cycle progression, and telomere and centromere structure and function. Here, we summarize the lines of evidence indicating that these epigenetic defects might represent a major factor in the pathophysiology of aging and aging-related diseases, especially cancer.
衰老 是一个多方面的过程,其特征是基因组中的遗传和表观遗传变化。衰老的遗传成分最初受到了所有关注。随着年龄增长,DNA损伤修复能力逐渐下降,导致端粒磨损和突变积累,仍然是基因组不稳定的主要原因。然而,表观遗传机制现已成为衰老过程中基因组结构和功能改变的关键因素。表观遗传调控的三大支柱是DNA甲基化、组蛋白修饰和非编码RNA种类。这些表观遗传机制的改变影响绝大多数核过程,包括基因转录和沉默、DNA复制和修复、细胞周期进程以及端粒和着丝粒的结构和功能。在这里,我们总结了一系列证据,表明这些表观遗传缺陷可能是衰老及衰老相关疾病(尤其是癌症)病理生理学的一个主要因素。