The point mutation of mitochondrial DNA characteristic for MERRF disease is found also in healthy people of different ages

FEBS Lett. 1993 Feb 8;317(1-2):27-30. doi: 10.1016/0014-5793(93)81484-h.


The A-to-G transition mutation in the tRNA(Lys) gene of mitochondrial DNA (mtDNA), characteristic for the maternally inherited MERRF syndrome (myoclonic epilepsy with ragged red fibers), has been identified by point mutation-specific polymerase chain reaction in extraocular muscle from 11 of 16 healthy people of different ages. No mutation was found in navel-string samples from 5 newborns, in HeLa cells, and in 2 individuals younger than 20 years. On the other hand, the mutation is present in all 5 tested 74-89-year-old individuals and in 6 of 9 20-70-year-old individuals. The amount of mutated from total mtDNA was estimated by 'mispairing PCR' in extraocular muscle of 2 individuals of 74 and 89 years to 2.0 and 2.4%, respectively. In most tissue samples the MERRF mutation occurs together with the 'common deletion' of mtDNA, which was previously shown to accumulate in healthy individuals with increasing age. It is proposed that during aging, deletions and point mutations of mtDNA accumulate, which could impair mitochondrial energetics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Base Sequence
  • DNA, Mitochondrial / genetics*
  • DNA, Single-Stranded
  • HeLa Cells
  • Humans
  • Infant, Newborn
  • Male
  • Middle Aged
  • Mitochondria, Muscle / metabolism
  • Mitochondrial Encephalomyopathies / genetics*
  • Molecular Sequence Data
  • Point Mutation*
  • Polymerase Chain Reaction


  • DNA, Mitochondrial
  • DNA, Single-Stranded