Copeland William C
Laboratory of Molecular Genetics, National Institute of Environmental Health Sciences, Durham, NC 27709, USA.
Subcell Biochem. 2010;50:211-22. doi: 10.1007/978-90-481-3471-7_11.
Since mutations in mitochondrial DNA (mtDNA) have been shown to be a cause of many mitochondrial diseases as well as aging, it is important to understand the origin of these mutations and how replication proteins modulate this process. DNA polymerase gamma (pol gamma) is the polymerase that is responsible for replication and repair of mtDNA. Pol gamma has three main roles in mtDNA maintenance and mutagenesis. As the only known DNA polymerase in mitochondria, pol gamma is required for all replication and repair functions and is the main source of errors produced in human mtDNA. Pol gamma is also sensitive to a host of antiviral nucleoside analogs used to treat HIV-1 infections, which can cause an induced mitochondrial toxicity. Finally, the gene for pol gamma, POLG, is a genetic locus for several mitochondrial disease with over 150 genetic mutations currently identified.
由于线粒体DNA(mtDNA)突变已被证明是许多线粒体疾病以及衰老的一个原因,因此了解这些突变的起源以及复制蛋白如何调节这一过程非常重要。DNA聚合酶γ(polγ)是负责mtDNA复制和修复的聚合酶。Polγ在mtDNA维持和诱变中具有三个主要作用。作为线粒体中唯一已知的DNA聚合酶,polγ对于所有复制和修复功能都是必需的,并且是人类mtDNA中产生错误的主要来源。Polγ也对用于治疗HIV-1感染的多种抗病毒核苷类似物敏感,这些类似物可导致诱导线粒体毒性。最后,polγ基因(POLG)是几种线粒体疾病的遗传位点,目前已鉴定出超过150种基因突变。