Brossas J Y, Barreau E, Courtois Y, Tréton J
Centre de Gérontologie, Association Claude Bernard, Paris, France.
Biochem Biophys Res Commun. 1994 Jul 29;202(2):654-9. doi: 10.1006/bbrc.1994.1980.
We report for the first time that multiple deletions occur during ageing of mice brain mitochondrial DNA (mtDNA). Deletions were detected by electrophoresis after amplification using the nested Polymerase Chain Reaction (N-PCR) method. Three mutant mtDNAs with 3726-, 3867- and 4236-bp deletions were directly detected by N-PCR which were undetectable in young brain mice. Each deletion was sequenced: in the region containing the junction fragment three different repeats of 13, 14 and 15 bp were observed. These results support the hypothesis that direct repeats are an initiating factor involved in ageing-associated accumulation of deletion.
我们首次报道,小鼠脑线粒体DNA(mtDNA)在衰老过程中会发生多个缺失。使用巢式聚合酶链反应(N-PCR)方法扩增后,通过电泳检测到缺失。通过N-PCR直接检测到三个分别缺失3726 bp、3867 bp和4236 bp的突变型mtDNA,而在幼龄小鼠脑中未检测到这些缺失。对每个缺失进行了测序:在包含连接片段的区域中,观察到13 bp、14 bp和15 bp的三种不同重复序列。这些结果支持了这样的假说,即直接重复序列是与衰老相关的缺失积累的起始因素。