Email updates

Keep up to date with the latest news and content from Genome Biology and BioMed Central.

Research news

Mitochondrial DNA homoplasmy

Jonathan B Weitzman

Author Affiliations

Genome Biology 2002, 3:spotlight-20020416-01  doi:10.1186/gb-spotlight-20020416-01


The electronic version of this article is the complete one and can be found online at:


Published:16 April 2002

© 2002 BioMed Central Ltd

Research news

Somatic point mutations in mitochondrial DNA (mtDNA) have been linked to aging and cancer. Each cell contains a large number of mtDNA molecules, so any mutation requires a process of clonal expansion in order to reach homoplasmy (close to 100%) and to exert a phenotypic influence. In the April 16 Proceedings of the National Academy of Sciences, Nekhaeva et al. document the frequency of mtDNA mutations in human tissues (Proc Natl Acad Sci USA 2002, 99:5521-5526). They employed a cell-by-cell sequence-specific method to study buccal epithelial cells and cardiomycoytes from aged individuals (up to 109 years old!). They present evidence for intercellular clonal expansion of mtDNA mutations in cells from aged tissues; they found that the rate of spread to homoplasmy was very rapid. The spectra of mtDNA mutations were different in the two cell types and probably reflect a difference in the mechanisms of clonal expansion. These results support the possible link between mtDNA mutations and aging, but suggest that mtDNA mutations in tumor cells probably appear by the same process as in normal cells.

References

  1. Mitochondrial DNA mutation associated with aging and degenerative disease.

    PubMed Abstract OpenURL

  2. Facile detection of mitochondrial DNA mutations in tumors and bodily fluids.

    PubMed Abstract | Publisher Full Text OpenURL

  3. [http://www.pnas.org] webcite

    Proceedings of the National Academy of Sciences

  4. Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy.

    PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL