Laboratory of Molecular Gerontology, National Institute on Aging, Intramural Research Program, National Institutes of Health, 251 Bayview Boulevard, Suite 100, Baltimore, MD 21224, USA.
Am J Hum Genet. 2019 Aug 1;105(2):237-257. doi: 10.1016/j.ajhg.2019.06.005.
Genetic information is constantly being attacked by intrinsic and extrinsic damaging agents, such as reactive oxygen species, atmospheric radiation, environmental chemicals, and chemotherapeutics. If DNA modifications persist, they can adversely affect the polymerization of DNA or RNA, leading to replication fork collapse or transcription arrest, or can serve as mutagenic templates during nucleic acid synthesis reactions. To combat the deleterious consequences of DNA damage, organisms have developed complex repair networks that remove chemical modifications or aberrant base arrangements and restore the genome to its original state. Not surprisingly, inherited or sporadic defects in DNA repair mechanisms can give rise to cellular outcomes that underlie disease and aging, such as transformation, apoptosis, and senescence. In the review here, we discuss several genetic disorders linked to DNA repair defects, attempting to draw correlations between the nature of the accumulating DNA damage and the pathological endpoints, namely cancer, neurological disease, and premature aging.
遗传信息不断受到内在和外在的损伤因素的攻击,如活性氧、大气辐射、环境化学物质和化疗药物。如果 DNA 修饰持续存在,它们可能会对 DNA 或 RNA 的聚合产生不利影响,导致复制叉崩溃或转录停滞,或者在核酸合成反应中作为诱变模板。为了应对 DNA 损伤的有害后果,生物体已经开发出复杂的修复网络,去除化学修饰或异常碱基排列,并将基因组恢复到原始状态。毫不奇怪,DNA 修复机制的遗传或散发性缺陷会导致疾病和衰老的细胞后果,如转化、细胞凋亡和衰老。在本文的综述中,我们讨论了几种与 DNA 修复缺陷相关的遗传疾病,试图在积累的 DNA 损伤的性质和病理终点之间建立相关性,即癌症、神经疾病和早衰。