Mitochondrial DNA mutations in disease and ageing

Novartis Found Symp. 2001:235:234-43; discussion 243-6. doi: 10.1002/0470868694.ch19.

Abstract

The chronological accumulation of mitochondrial DNA mutations has been proposed as a potential mechanism in the physiological processes of ageing and age-related disease. We discuss the evidence behind this theory and relate some of the ageing mitochondrial changes to mitochondrial DNA disorders. In particular, we describe the aggregation of cytochrome c oxidase-deficient cells in both skeletal muscle and the CNS in normal ageing as seen in the mitochondrial DNA disorders. These mitochondrial enzyme-deficient cells have been shown to occur in significant quantities in both muscle and CNS in patients with mitochondrial DNA disorders. In both ageing and mtDNA disorder muscle these cytochrome c-deficient fibres contain high levels of a single mutant strain of mitochondrial DNA. Whether these mutations are a primary or secondary event in the physiology of ageing remains to be determined.

Publication types

  • Review

MeSH terms

  • Aging / genetics*
  • Animals
  • DNA, Mitochondrial / genetics*
  • Disease
  • Electron Transport Complex IV / metabolism
  • Genetic Diseases, Inborn / genetics*
  • Humans
  • Mitochondria
  • Mutation*

Substances

  • DNA, Mitochondrial
  • Electron Transport Complex IV