Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778

J Hum Genet. 1998;43(4):242-5. doi: 10.1007/s100380050081.

Abstract

We examined for mitochondrial DNA (mtDNA) mutations at nucleotide positions(nt) 3460, 14,484, 9438, 9804, and 15,257 in ten Japanese patients with idiopathic optic neuropathy unassociated with a mutation at nt11,778. The mtDNAs were amplified by polymerase chain reaction (PCR), the products were digested with restriction enzymes, and the sizes of the fragments were analyzed on 8% polyacrylamide gel. Of the ten patients, one had an mtDNA mutation at nt3460 and another patient had a mutation at nt14,484. We suggest that mtDNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nt11,778 should be further investigated.

MeSH terms

  • Adolescent
  • Adult
  • Child
  • DNA Mutational Analysis
  • DNA, Mitochondrial / chemistry*
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • Female
  • Humans
  • Japan
  • Male
  • Mutation*
  • Optic Atrophies, Hereditary / genetics*
  • Polymerase Chain Reaction

Substances

  • DNA, Mitochondrial
  • Deoxyribonucleases, Type II Site-Specific
  • GATC-specific type II deoxyribonucleases