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Quantification of global mitochondrial DNA methylation levels and inverse correlation with age at two CpG sites

机译:在两个CpG位点定量检测线粒体DNA甲基化水平并与年龄成反比

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摘要

Mammalian ageing features biological attrition evident at cellular, genetic and epigenetic levels. Mutation of mitochondrial DNA, and nuclear DNA methylation changes are well established correlates of ageing. The methylation of mitochondrial DNA (mtDNA) is a new and incompletely described phenomenon with unknown biological control and significance. Here we describe the bisulphite sequencing of mtDNA from 82 individuals aged 18-91 years. We detected low and variable levels of mtDNA methylation at 54 of 133 CpG sites interrogated. Regression analysis of methylation levels at two CpG sites (M1215 and M1313) located within the 12S ribosomal RNA gene showed an inverse correlation with subject age suggesting their utility as epigenetic markers of ageing.
机译:哺乳动物的衰老具有在细胞,遗传和表观遗传水平上明显的生物耗损。线粒体DNA突变和核DNA甲基化变化是衰老的相关因素。线粒体DNA(mtDNA)的甲基化是一种新的且描述不完整的现象,具有未知的生物学控制和意义。在这里,我们描述了来自82位18-91岁个体的mtDNA亚硫酸氢盐测序。我们在被讯问的133个CpG位点中的54个中检测到了低水平和可变水平的mtDNA甲基化。位于12S核糖体RNA基因内的两个CpG位点(M1215和M1313)的甲基化水平的回归分析显示与受试者年龄呈负相关,表明它们可作为衰老的表观遗传标记。

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