Multiple deletions of mtDNA remove the light strand origin of replication

被引:12
作者
Bank, C
Soulimane, T
Schröder, JM
Buse, G
Zanssen, S
机构
[1] Univ Klinikum Rhein Westfal TH Aachen, Inst Biochem, D-52074 Aachen, Germany
[2] Univ Klinikum Rhein Westfal TH Aachen, Inst Neuropathol, D-52074 Aachen, Germany
关键词
muscle; inflammatory myopathies; inclusion body myositis; mtDNA deletions; aging;
D O I
10.1006/bbrc.2000.3951
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Idiopathic inflammatory myopathies are progressive, debilitating muscle diseases. The pathogenesis of these disorders is multifactorial and appears to include mutations of the mitochondrial genome, which are usually indicated by morphological changes of mitochondria. The vast majority of all mitochondrial DNA deletions found are located between the origins of replication in the "major region" between nt5760-nt190. Using long distance PCR and sequencing techniques, me detected deletions which were unusually large (ca. 10500-12800 bp) and show uncommon 5'-breakpoints between nt800 and nt3326. Unlike most other deletions, their breakpoints are far upstream of the "major region." The atypical location of these deletions suggests a different pathomechanism. The impact of the mitochondrial DNA deletions in the pathogenetic cascade remains uncertain. (C) 2000 Academic Press.
引用
收藏
页码:595 / 601
页数:7
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