A mitochondrial tRNA anticodon swap associated with a muscle disease

Nat Genet. 1993 Jul;4(3):284-8. doi: 10.1038/ng0793-284.


We have identified an unusual mitochondrial (mt) tRNA mutation in a seven year-old girl with a pure myopathy. This G to A transition at mtDNA position 15990 changed the anticodon normally found in proline tRNAs (UGG) to the one found in serine tRNAs (UGA), and is the first pathogenic anticodon alteration described in a higher eukaryote. The mutant mtDNA was heteroplasmic (85% mutant) in muscle but was undetectable in white blood cells from the patient and her mother. Analysis of single muscle fibres indicated that mutant mtDNAs severely impaired mitochondrial protein synthesis and respiratory chain activity, but only when present at greater than 90%. The recessive behaviour of this mtDNA alteration may explain the patient's relatively mild clinical phenotype.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Anticodon / genetics*
  • Base Sequence
  • Child
  • DNA, Mitochondrial / genetics
  • DNA, Mitochondrial / metabolism
  • Female
  • Humans
  • Mitochondrial Myopathies / genetics*
  • Mitochondrial Myopathies / metabolism
  • Molecular Sequence Data
  • Muscle Proteins / biosynthesis
  • Muscle Proteins / genetics
  • Muscles / metabolism
  • Pedigree
  • Phenotype
  • Point Mutation
  • RNA / genetics*
  • RNA, Mitochondrial
  • RNA, Transfer, Pro / genetics
  • RNA, Transfer, Ser / genetics
  • Tissue Distribution


  • Anticodon
  • DNA, Mitochondrial
  • Muscle Proteins
  • RNA, Mitochondrial
  • RNA, Transfer, Pro
  • RNA, Transfer, Ser
  • RNA