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pubmed-article:1660306pubmed:abstractTextIn situ hybridization studies were performed on a series of chronic progressive external ophthalmoplegia patients harbouring large mitochondrial DNA deletions, using intra- and extra-deletional probes. Clear differences in the distribution of wild type and deleted mitochondrial genomes were seen in both ragged-red and non-ragged red, cytochrome c oxidase-negative fibres, with an accumulation of deleted genomes in the subsarcolemmal zone. Wild type genome content was normal or decreased in the cytochrome c oxidase-negative regions of one case, but in two patients, wild type mtDNA content in cytochrome c oxidase-negative regions was either normal (most fibres) or increased (occasional fibres). The latter observation suggests there may be a stage in the natural history of ragged-red fibre evolution where wild type genomes are transiently increased. The significance of this finding is discussed.lld:pubmed
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pubmed-article:1660306pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:1660306pubmed:articleTitleMitochondrial genome distribution in histochemically cytochrome c oxidase-negative muscle fibres in patients with a mixture of deleted and wild type mitochondrial DNA.lld:pubmed
pubmed-article:1660306pubmed:affiliationDepartment of Neurology, St. Vincent's Hospital, Melbourne, Australia.lld:pubmed
pubmed-article:1660306pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1660306pubmed:publicationTypeComparative Studylld:pubmed
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