Larsson N G, Holme E
Department of Clinical Chemistry, Gothenburg University, Sahlgren's Hospital, Sweden.
Biochim Biophys Acta. 1992 Aug 25;1139(4):311-4. doi: 10.1016/0925-4439(92)90106-w.
We have sequenced the breakpoints of deleted mtDNA in muscle from four children with mitochondrial myopathy and multisystem mitochondrial disorders. The deletions were 4884, 6067, 7663 and 7150 base pairs (bp) in size and affected several protein and transfer RNA genes. The sequences needed for transcription and replication of mtDNA were not affected in any case. The deletions were flanked by direct short repeats in all cases. Multiple repeats were found in case 1 and 4. Imperfect repeats were found in case 3 and 4 and this made it possible to distinguish the repeats 5' and 3' to the deletion. In both cases the 3' repeat was retained. The deletion of 7663 bp in case 3 has been reported in two other cases and may represent a second hotspot for mtDNA deletions in addition to the common deletion of 4977 bp found in one third of cases. A comparison of the breakpoint sequence of case 3 with the two other reported cases revealed that when a deletion is formed between the same repeats in different patients either the 5' or 3' repeat can be retained. This study shows that both single and multiple repeats can be associated with single mtDNA deletions and that both 5' and 3' repeated sequences can be retained. These findings are consistent with the slip-replication model for the generation of mtDNA deletions.
我们对4名患有线粒体肌病和多系统线粒体疾病的儿童肌肉中缺失的线粒体DNA(mtDNA)断点进行了测序。这些缺失片段大小分别为4884、6067、7663和7150个碱基对(bp),影响了多个蛋白质和转运RNA基因。在任何情况下,mtDNA转录和复制所需的序列均未受影响。所有病例中,缺失片段两侧均有直接短重复序列。在病例1和病例4中发现了多个重复序列。在病例3和病例4中发现了不完全重复序列,这使得区分缺失片段5'端和3'端的重复序列成为可能。在这两个病例中,3'端重复序列均得以保留。病例3中7663 bp的缺失在另外两个病例中也有报道,除了三分之一病例中常见的4977 bp缺失外,这可能代表了mtDNA缺失的另一个热点区域。将病例3的断点序列与另外两个报道病例进行比较发现,当不同患者在相同重复序列之间形成缺失时,5'端或3'端重复序列均可保留。本研究表明,单个和多个重复序列均可与单个mtDNA缺失相关,且5'端和3'端重复序列均可保留。这些发现与mtDNA缺失产生的滑动复制模型一致。