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Nat Genet. 1992 Aug;1(5):359-67.

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions.

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1
H. Houston Merritt Clinical Research Center for Muscular Dystrophy and Related Disorders, New York, New York.

Abstract

Large-scale deletions of mitochondrial DNA (mtDNA) are associated with a subgroup of mitochondrial encephalomyopathies. We studied seven patients with Kearns-Sayre syndrome or isolated ocular myopathy who harboured a sub-population of partially-deleted mitochondrial genomes in skeletal muscle. Variable cytochrome c oxidase (COX) deficiencies and reduction of mitochondrially-encoded polypeptides were found in affected muscle fibres, but while many COX-deficient fibres had increased levels of mutant mtDNA, they almost invariably had reduced levels of normal mtDNA. Our results suggest that a specific ratio between mutant and wild-type mitochondrial genomes is the most important determinant of a focal respiratory chain deficiency, even though absolute copy numbers may vary widely.

PMID:
1284549
DOI:
10.1038/ng0892-359
[Indexed for MEDLINE]
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