Newton R K, Ducore J M, Sohal R S
Department of Biological Sciences, Southern Methodist University, Dallas, TX 75275.
Mutat Res. 1989 Mar;219(2):113-20. doi: 10.1016/0921-8734(89)90022-2.
It has been suggested that genomic alterations involving DNA damage and the ability to repair such damage play an important role in cellular senescence. In this study, endogenous DNA single-strand breaks, the susceptibility of DNA to induced strand breakage and the capacity to repair these breaks were compared in postmitotic cells from young (3-day-old) and old (23-day-old) houseflies. DNA single-strand breaks did not accumulate during normal aging in the housefly. However, cells of the old flies exhibited a greater sensitivity to single-strand breakage induced by gamma-radiation and UV light. The capacity to repair these exogenously induced single-strand breaks declined with age. Results do not support the view that DNA single-strand breaks are a causal factor in aging in the housefly. An age-related increase in the susceptibility to undergo single-strand breakage suggests alterations in chromatin during the aging process.
有人提出,涉及DNA损伤以及修复此类损伤能力的基因组改变在细胞衰老中起重要作用。在本研究中,比较了来自年轻(3日龄)和年老(23日龄)家蝇的有丝分裂后细胞中的内源性DNA单链断裂、DNA对诱导链断裂的敏感性以及修复这些断裂的能力。在家蝇正常衰老过程中,DNA单链断裂不会积累。然而,年老家蝇的细胞对γ射线和紫外线诱导的单链断裂表现出更高的敏感性。修复这些外源性诱导的单链断裂的能力随年龄增长而下降。结果不支持DNA单链断裂是家蝇衰老的因果因素这一观点。对单链断裂敏感性的年龄相关增加表明衰老过程中染色质发生了改变。