Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Campus Belval, 7, avenue des Hauts-Fourneaux, 4362 Esch-sur-Alzette, Luxembourg.
Biogerontology. 2012 Oct;13(5):557-64. doi: 10.1007/s10522-012-9390-7. Epub 2012 Aug 3.
Mutations arise during DNA replication due to oxidative lesions and intrinsic polymerase errors. Mitochondrial DNA (mtDNA) mutation rate is therefore closely linked to the mitochondrial DNA turnover process, especially in post mitotic cells. This makes the mitochondrial DNA turnover rate critical for understanding the origin and dynamics of mtDNA mutagenesis in post mitotic cells. Experimental mitochondrial turnover quantification has been based on different mitochondrial macromolecules, such as mitochondrial proteins, lipids and DNA, and the experimental data suggested highly divergent turnover rates, ranging from over 2 days to about 1 year. In this article we argue that mtDNA turnover rate cannot be as fast as is often envisaged. Using a stochastic model based on the chemical master equation, we show that a turnover rate corresponding to mtDNA half-life in the order of months is the most consistent with published mtDNA mutation levels.
由于氧化损伤和内在聚合酶错误,DNA 复制过程中会产生突变。因此,线粒体 DNA(mtDNA)的突变率与线粒体 DNA 周转过程密切相关,尤其是在后有丝分裂细胞中。这使得线粒体 DNA 周转速率成为理解后有丝分裂细胞中线粒体 DNA 诱变的起源和动态的关键。实验性线粒体周转的定量研究是基于不同的线粒体大分子,如线粒体蛋白、脂质和 DNA,实验数据表明周转速率差异很大,从超过 2 天到大约 1 年不等。在本文中,我们认为 mtDNA 周转速率不可能像通常想象的那么快。我们使用基于化学主方程的随机模型表明,与几个月内 mtDNA 半衰期相对应的周转率与已发表的 mtDNA 突变水平最为一致。