4.5 Article

Mitochondrial DNA repair and damage tolerance

期刊

FRONTIERS IN BIOSCIENCE-LANDMARK
卷 22, 期 -, 页码 920-943

出版社

FRONTIERS IN BIOSCIENCE INC
DOI: 10.2741/4525

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

资金

  1. National Science Foundation [MCB0841857, MCB1243428]
  2. Div Of Molecular and Cellular Bioscience
  3. Direct For Biological Sciences [1243428] Funding Source: National Science Foundation

向作者/读者索取更多资源

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.

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