Sun Xin, Lee William, Vaghjiani Vijesh, St John Justin C
Mitochondrial Genetics Group, Centre for Genetic Diseases, Hudson Institute of Medical Research, 27-31 Wright Street, Clayton, VIC, 3168, Australia.
The Department of Molecular and Translational Science, Monash University, 27-31 Wright Street, Clayton, VIC, 3168, Australia.
Methods Mol Biol. 2016;1351:131-41. doi: 10.1007/978-1-4939-3040-1_10.
Replication of mitochondrial DNA (mtDNA) is important for ensuring that cells have sufficient mtDNA copy number to meet their specific requirements for the generation of cellular energy through oxidative phosphorylation. A number of transcription and replication factors are required for this process, with a key factor being the nuclear-encoded mtDNA-specific DNA polymerase γ. DNA polymerase γ has a catalytic subunit (POLGA), whose gene has been shown to be DNA methylated at exon 2. This methylation is considered to be one of the key mechanisms that regulate mtDNA copy number. These findings have made it of great importance to establish optimal methods for investigating the effects of DNA methylation on mtDNA replication. Here, we provide methods to determine the extent of DNA methylation at exon 2 of POLGA as well as other gene targets of interest. We also show how mtDNA copy number is assessed and, from these two outputs, define the efficiency of mtDNA replication by calculating the mtDNA-replicative efficiency index.
线粒体DNA(mtDNA)的复制对于确保细胞拥有足够的mtDNA拷贝数至关重要,以便通过氧化磷酸化满足其产生细胞能量的特定需求。这一过程需要多种转录和复制因子,其中关键因子是核编码的mtDNA特异性DNA聚合酶γ。DNA聚合酶γ有一个催化亚基(POLGA),其基因已被证明在外显子2处发生DNA甲基化。这种甲基化被认为是调节mtDNA拷贝数的关键机制之一。这些发现使得建立研究DNA甲基化对mtDNA复制影响的最佳方法变得极为重要。在此,我们提供了确定POLGA外显子2以及其他感兴趣基因靶点处DNA甲基化程度的方法。我们还展示了如何评估mtDNA拷贝数,并根据这两个结果,通过计算mtDNA复制效率指数来定义mtDNA复制的效率。