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Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies.
Filosto, Massimiliano; Mancuso, Michelangelo; Vives-Bauza, Cristofol; Vilà, Maya R; Shanske, Sara; Hirano, Michio; Andreu, Antoni L; DiMauro, Salvatore.
Afiliação
  • Filosto M; Department of Neurology, Columbia University College of Physicians and Surgeons, New York, NY, USA.
Ann Neurol ; 54(4): 524-6, 2003 Oct.
Article em En | MEDLINE | ID: mdl-14520667
ABSTRACT
In 2002, paternal inheritance of muscle mitochondrial DNA (mtDNA) was reported in a patient with exercise intolerance and a mitochondrial DNA (mtDNA) mutation restricted to skeletal muscle. To evaluate whether paternal inheritance is a common phenomenon, we studied 10 sporadic patients with skeletal muscle-restricted mtDNA mutations five harbored mtDNA point mutations in protein-coding genes and five had single mtDNA deletions. We performed haplotype analysis and direct sequencing of the hypervariable regions 1 and 2 of the D-loop in muscle and blood from the patients and, when available, in blood from their parents. We did not observe paternal inheritance in any of our patients.
Assuntos
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Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Miopatias Mitocondriais / Mutação Idioma: En Ano de publicação: 2003 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Miopatias Mitocondriais / Mutação Idioma: En Ano de publicação: 2003 Tipo de documento: Article