Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology, Heraklion, Greece; Department of Biology, University of Crete, Heraklion, Greece.
Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology, Heraklion, Greece; Department of Biology, University of Crete, Heraklion, Greece.
J Invest Dermatol. 2021 Apr;141(4S):961-967. doi: 10.1016/j.jid.2020.10.006. Epub 2021 Jan 22.
In mammals, genome instability and aging are intimately linked as illustrated by the growing list of patients with progeroid and animal models with inborn DNA repair defects. Until recently, DNA damage was thought to drive aging by compromising transcription or DNA replication, thereby leading to age-related cellular malfunction and somatic mutations triggering cancer. However, recent evidence suggests that DNA lesions also elicit widespread epigenetic alterations that threaten cell homeostasis as a function of age. In this review, we discuss the functional links of persistent DNA damage with the epigenome in the context of aging and age-related diseases.
在哺乳动物中,基因组不稳定性和衰老密切相关,这一点可以从越来越多的具有早衰表型的患者和具有先天 DNA 修复缺陷的动物模型中得到证实。直到最近,人们还认为 DNA 损伤通过损害转录或 DNA 复制来驱动衰老,从而导致与年龄相关的细胞功能障碍和引发癌症的体细胞突变。然而,最近的证据表明,DNA 损伤也会引发广泛的表观遗传改变,这些改变会随着年龄的增长威胁到细胞的内稳态。在这篇综述中,我们讨论了在衰老和与年龄相关的疾病背景下,持续的 DNA 损伤与表观基因组之间的功能联系。