Tissue-specific involvement of multiple mitochondrial DNA deletions in familial mitochondrial myopathy

Biochem Biophys Res Commun. 1998 Jun 9;247(1):24-7. doi: 10.1006/bbrc.1998.8709.

Abstract

It is still uncertain how deleted mitochondrial DNA (mtDNA) is distributed to each tissue during development, although deletions of mtDNA have been extensively observed in various pathologic conditions. This paper presents two Japanese siblings with progressive external ophthalmoplegia exhibiting multiple mtDNA deletions. In one patient, similar multiple mtDNA deletions were found in skeletal muscle specimens as well as in the spinal cord but not in the myocardium, liver or leukocytes. A similar deletion pattern was found in the skeletal muscle but not in the leukocytes of the other patient. The results suggest the complex mechanism to generate, expand and eliminate the deleted mtDNA in humans.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Blotting, Southern
  • DNA, Mitochondrial / genetics*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mitochondrial Myopathies / genetics*
  • Mitochondrial Myopathies / pathology
  • Muscle, Skeletal / pathology
  • Organ Specificity / genetics
  • Pedigree
  • Polymerase Chain Reaction
  • Sequence Deletion*
  • Spinal Cord / pathology

Substances

  • DNA, Mitochondrial