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The age-associated decrease in the amount of amplifiable full-lengthmitochondrial DNA in human skeletal muscle

机译:与年龄相关的人类骨骼肌中可扩增的全长线粒体DNA数量减少

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There has been a continuous evolution in our concept [1] that mtDNA undergoes a range of mutations with age and that such alterations lead to a decline in mitochondrial bioenergy capacity. Here we report that a wide range of deletion mutations accumulate with age and the amount of full-length mtDNA (FLmtDNA) amplifiable by extra-long PCR (XL-PCR) markedly decreases with age. An analysis of single human quadriceps muscle fibres reveals a close correlation between the decrease in FLmtDNA and the decline in cytochrome c oxidase activity, an exemplifier of mitochondrial bioenergy. However, Southern blotting analysis of unamplified genomic DNA shows that there is little decrease in FLmtDNA in aged quadriceps. The results are interpreted to indicate that while there is little change in the total mtDNA with age, nonetheless a significant proportion of this mtDNA is extensively damaged such that it cannot be amplified by XL-PCR. The amplifiable FLmtDNA, which putatively represents the functional component of the mtDNA, decreases markedly with age.
机译:我们的概念一直在不断发展[1],即随着年龄的增长,mtDNA会发生一系列突变,并且这种改变会导致线粒体生物能量的下降。在这里,我们报告说,随着年龄的增长,大量的缺失突变会累积,通过超长PCR(XL-PCR)扩增的全长mtDNA(FLmtDNA)的数量会随着年龄的增长而显着减少。对单个人股四头肌肌肉纤维的分析显示,FLmtDNA的下降与线粒体生物能量的例证细胞色素C氧化酶活性的下降之间存在密切的相关性。然而,对未扩增的基因组DNA的Southern印迹分析表明,在老年股四头肌中FLmtDNA几乎没有下降。解释结果表明,尽管总mtDNA随年龄变化不大,但是该mtDNA的很大一部分受到了广泛破坏,因此无法通过XL-PCR进行扩增。假定代表mtDNA的功能成分的可扩增FLmtDNA随着年龄的增长而显着下降。

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