Replication and Transcription of Human Mitochondrial DNA

被引:2
|
作者
Falkenberg, Maria [1 ]
Larsson, Nils-Goran [2 ]
Gustafsson, Claes M. [1 ]
机构
[1] Univ Gothenburg, Inst Biomed, Dept Med Biochem & Cell Biol, Gothenburg, Sweden
[2] Karolinska Inst, Dept Med Biochem & Biophys, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
mitochondria; mtDNA; replication; transcription; nucleoid; MOUSE L-CELLS; LIGHT-STRAND TRANSCRIPTION; STRUCTURE-FUNCTION DEFECTS; TERMINATION FACTOR MTERF; RNA-POLYMERASE; HEAVY-STRAND; RIBOSOMAL-RNA; ACCESSORY SUBUNIT; D-LOOP; INTRAMITOCHONDRIAL FIBERS;
D O I
10.1146/annurev-biochem-052621-092014
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
Mammalian mitochondrial DNA (mtDNA) is replicated and transcribed by phage-like DNA and RNA polymerases, and our understanding of these processes has progressed substantially over the last several decades. Molecular mechanisms have been elucidated by biochemistry and structural biology and essential in vivo roles established by cell biology and mouse genetics. Single molecules of mtDNA are packaged by mitochondrial transcription factor A into mitochondrial nucleoids, and their level of compaction influences the initiation of both replication and transcription. Mutations affecting the molecular machineries replicating and transcribing mtDNA are important causes of human mitochondrial disease, reflecting the critical role of the genome in oxidative phosphorylation system biogenesis. Mechanisms controlling mtDNA replication and transcription still need to be clarified, and future research in this area is likely to open novel therapeutic possibilities for treating mitochondrial dysfunction.
引用
收藏
页码:47 / 77
页数:31
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