线粒体DNA
DNA修复
生物
线粒体
核DNA
DNA损伤
基因组
细胞生物学
DNA
遗传学
线粒体融合
人类线粒体遗传学
基因
作者
Rebeca R. Alencar,Caio M.P.F. Batalha,Thiago S. Freire,Nadja Cristhina de Souza-Pinto
出处
期刊:The Enzymes
[Elsevier BV]
日期:2019-01-01
卷期号:45: 257-287
被引量:28
标识
DOI:10.1016/bs.enz.2019.06.002
摘要
The mitochondrial genome encodes proteins essential for the oxidative phosphorylation and, consequently, for proper mitochondrial function. Its localization and, possibly, structural organization contribute to higher DNA damage accumulation, when compared to the nuclear genome. In addition, the mitochondrial genome mutates at rates several times higher than the nuclear, although the causal relationship between these events are not clearly established. Maintaining mitochondrial DNA stability is critical for cellular function and organismal fitness, and several pathways contribute to that, including damage tolerance and bypass, degradation of damaged genomes and DNA repair. Despite initial evidence suggesting that mitochondria lack DNA repair activities, most DNA repair pathways have been at least partially characterized in mitochondria from several model organisms, including humans. In this chapter, we review what is currently known about how the main DNA repair pathways operate in mitochondria and contribute to mitochondrial DNA stability, with focus on the enzymology of mitochondrial DNA repair.
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