Mitochondrial DNA repair and damage tolerance

被引:53
作者
Stein, Alexis [1 ]
Sia, Elaine A. [1 ]
机构
[1] Univ Rochester, Dept Biol, RC Box 270211, Rochester, NY 14627 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2017年 / 22卷
基金
美国国家科学基金会;
关键词
Review; Mitochondrial DNA; mtDNA; DNA Repair; Base Excision Repair; BER; Mismatch Repair; MMR; Homologous Recombination; HR; Non-homologous End Joining; NHEJ; mtDNA Degradation; Translesion Synthesis; TLS; Microhomology-mediated End Joining; MMEJ; Yeast; BASE EXCISION-REPAIR; STRAND BREAK REPAIR; CRUCIFORM CUTTING ENDONUCLEASE; ULTRAVIOLET-RADIATION EXPOSURE; SACCHAROMYCES-CEREVISIAE; MISMATCH-REPAIR; MAMMALIAN MITOCHONDRIA; YEAST MITOCHONDRIA; OXIDATIVE STRESS; HUMAN-CELLS;
D O I
10.2741/4525
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The accurate maintenance of mitochondrial DNA (mtDNA) is required in order for eukaryotic cells to assemble a functional electron transport chain. This independently-maintained genome relies on nuclear-encoded proteins that are imported into the mitochondria to carry out replication and repair processes. Decades of research has made clear that mitochondria employ robust and varied mtDNA repair and damage tolerance mechanisms in order to ensure the proper maintenance of the mitochondrial genome. This review focuses on our current understanding of mtDNA repair and damage tolerance pathways including base excision repair, mismatch repair, homologous recombination, non-homologous end joining, translesion synthesis and mtDNA degradation in both yeast and mammalian systems.
引用
收藏
页码:920 / 943
页数:24
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