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衰老过程中的DNA损伤、突变与精细结构DNA修复

DNA damage, mutation and fine structure DNA repair in aging.

作者信息

Bohr V A, Anson R M

机构信息

Laboratory of Molecular Genetics, National Institutes on Aging, NIH, Baltimore, MD 21224, USA.

出版信息

Mutat Res. 1995 Oct;338(1-6):25-34. doi: 10.1016/0921-8734(95)00008-t.

Abstract

The primary focus of this review is on correlations found between DNA damage, repair, and aging. New techniques for the measurement of DNA damage and repair at the level of individual genes, in individual DNA strands and in individual nucleotides will allow us to gain information regarding the nature of these correlations. Fine structure studies of DNA damage and repair in specific regions, including active genes, telomeres, and mitochondria have begun. Considerable intragenomic DNA repair heterogeneity has been found, and there have been indications of relationships between aging and repair in specific regions. More studies are necessary, however, particularly studies of the repair of endogenous damage. It is emphasized that the information obtained must be viewed from a perspective that takes into account the total responses of the cell to damaging events and the inter-relationships that exist between DNA repair and transcription.

摘要

本综述的主要重点是在DNA损伤、修复与衰老之间发现的相关性。在单个基因、单个DNA链和单个核苷酸水平上测量DNA损伤和修复的新技术,将使我们能够获得有关这些相关性本质的信息。对包括活性基因、端粒和线粒体在内的特定区域的DNA损伤和修复的精细结构研究已经开始。已经发现了相当大的基因组内DNA修复异质性,并且有迹象表明特定区域的衰老与修复之间存在关联。然而,还需要更多的研究,特别是对内源性损伤修复的研究。需要强调的是,所获得的信息必须从一个考虑细胞对损伤事件的整体反应以及DNA修复与转录之间存在的相互关系的角度来审视。

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