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American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 2000 Apr 7;66(5):1599–1609. doi: 10.1086/302902

The mutation rate in the human mtDNA control region.

S Sigurğardóttir 1, A Helgason 1, J R Gulcher 1, K Stefansson 1, P Donnelly 1
PMCID: PMC1378010  PMID: 10756141

Abstract

The mutation rate of the mitochondrial control region has been widely used to calibrate human population history. However, estimates of the mutation rate in this region have spanned two orders of magnitude. To readdress this rate, we sequenced the mtDNA control region in 272 individuals, who were related by a total of 705 mtDNA transmission events, from 26 large Icelandic pedigrees. Three base substitutions were observed, and the mutation rate across the two hypervariable regions was estimated to be 3/705 =.0043 per generation (95% confidence interval [CI].00088-.013), or.32/site/1 million years (95% CI.065-.97). This study is substantially larger than others published, which have directly assessed mtDNA mutation rates on the basis of pedigrees, and the estimated mutation rate is intermediate among those derived from pedigree-based studies. Our estimated rate remains higher than those based on phylogenetic comparisons. We discuss possible reasons for-and consequences of-this discrepancy. The present study also provides information on rates of insertion/deletion mutations, rates of heteroplasmy, and the reliability of maternal links in the Icelandic genealogy database.

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Selected References

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  1. Awadalla P., Eyre-Walker A., Smith J. M. Linkage disequilibrium and recombination in hominid mitochondrial DNA. Science. 1999 Dec 24;286(5449):2524–2525. doi: 10.1126/science.286.5449.2524. [DOI] [PubMed] [Google Scholar]
  2. Bendall K. E., Macaulay V. A., Baker J. R., Sykes B. C. Heteroplasmic point mutations in the human mtDNA control region. Am J Hum Genet. 1996 Dec;59(6):1276–1287. [PMC free article] [PubMed] [Google Scholar]
  3. Bendall K. E., Macaulay V. A., Sykes B. C. Variable levels of a heteroplasmic point mutation in individual hair roots. Am J Hum Genet. 1997 Dec;61(6):1303–1308. doi: 10.1086/301636. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cann R. L., Stoneking M., Wilson A. C. Mitochondrial DNA and human evolution. Nature. 1987 Jan 1;325(6099):31–36. doi: 10.1038/325031a0. [DOI] [PubMed] [Google Scholar]
  5. Di Rienzo A., Wilson A. C. Branching pattern in the evolutionary tree for human mitochondrial DNA. Proc Natl Acad Sci U S A. 1991 Mar 1;88(5):1597–1601. doi: 10.1073/pnas.88.5.1597. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hauswirth W. W., Clayton D. A. Length heterogeneity of a conserved displacement-loop sequence in human mitochondrial DNA. Nucleic Acids Res. 1985 Nov 25;13(22):8093–8104. doi: 10.1093/nar/13.22.8093. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Helgason A., Sigureth ardóttir S., Gulcher J. R., Ward R., Stefánsson K. mtDNA and the origin of the Icelanders: deciphering signals of recent population history. Am J Hum Genet. 2000 Mar;66(3):999–1016. doi: 10.1086/302816. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Horai S., Hayasaka K., Kondo R., Tsugane K., Takahata N. Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs. Proc Natl Acad Sci U S A. 1995 Jan 17;92(2):532–536. doi: 10.1073/pnas.92.2.532. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Howell N., Kubacka I., Mackey D. A. How rapidly does the human mitochondrial genome evolve? Am J Hum Genet. 1996 Sep;59(3):501–509. [PMC free article] [PubMed] [Google Scholar]
  10. Jazin E., Soodyall H., Jalonen P., Lindholm E., Stoneking M., Gyllensten U. Mitochondrial mutation rate revisited: hot spots and polymorphism. Nat Genet. 1998 Feb;18(2):109–110. doi: 10.1038/ng0298-109. [DOI] [PubMed] [Google Scholar]
  11. Macaulay V. A., Richards M. B., Forster P., Bendall K. E., Watson E., Sykes B., Bandelt H. J. mtDNA mutation rates--no need to panic. Am J Hum Genet. 1997 Oct;61(4):983–990. doi: 10.1016/S0002-9297(07)64211-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Meyer S., Weiss G., von Haeseler A. Pattern of nucleotide substitution and rate heterogeneity in the hypervariable regions I and II of human mtDNA. Genetics. 1999 Jul;152(3):1103–1110. doi: 10.1093/genetics/152.3.1103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Michikawa Y., Mazzucchelli F., Bresolin N., Scarlato G., Attardi G. Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication. Science. 1999 Oct 22;286(5440):774–779. doi: 10.1126/science.286.5440.774. [DOI] [PubMed] [Google Scholar]
  14. Nickerson D. A., Tobe V. O., Taylor S. L. PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing. Nucleic Acids Res. 1997 Jul 15;25(14):2745–2751. doi: 10.1093/nar/25.14.2745. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Parsons T. J., Muniec D. S., Sullivan K., Woodyatt N., Alliston-Greiner R., Wilson M. R., Berry D. L., Holland K. A., Weedn V. W., Gill P. A high observed substitution rate in the human mitochondrial DNA control region. Nat Genet. 1997 Apr;15(4):363–368. doi: 10.1038/ng0497-363. [DOI] [PubMed] [Google Scholar]
  16. Richards M., Côrte-Real H., Forster P., Macaulay V., Wilkinson-Herbots H., Demaine A., Papiha S., Hedges R., Bandelt H. J., Sykes B. Paleolithic and neolithic lineages in the European mitochondrial gene pool. Am J Hum Genet. 1996 Jul;59(1):185–203. [PMC free article] [PubMed] [Google Scholar]
  17. Sajantila A., Lahermo P., Anttinen T., Lukka M., Sistonen P., Savontaus M. L., Aula P., Beckman L., Tranebjaerg L., Gedde-Dahl T. Genes and languages in Europe: an analysis of mitochondrial lineages. Genome Res. 1995 Aug;5(1):42–52. doi: 10.1101/gr.5.1.42. [DOI] [PubMed] [Google Scholar]
  18. Soodyall H., Jenkins T., Mukherjee A., du Toit E., Roberts D. F., Stoneking M. The founding mitochondrial DNA lineages of Tristan da Cunha Islanders. Am J Phys Anthropol. 1997 Oct;104(2):157–166. doi: 10.1002/(SICI)1096-8644(199710)104:2<157::AID-AJPA2>3.0.CO;2-W. [DOI] [PubMed] [Google Scholar]
  19. Stoneking M., Sherry S. T., Redd A. J., Vigilant L. New approaches to dating suggest a recent age for the human mtDNA ancestor. Philos Trans R Soc Lond B Biol Sci. 1992 Aug 29;337(1280):167–175. doi: 10.1098/rstb.1992.0094. [DOI] [PubMed] [Google Scholar]
  20. Tremblay M., Vézina H. New estimates of intergenerational time intervals for the calculation of age and origins of mutations. Am J Hum Genet. 2000 Feb;66(2):651–658. doi: 10.1086/302770. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Ward R. H., Frazier B. L., Dew-Jager K., Päbo S. Extensive mitochondrial diversity within a single Amerindian tribe. Proc Natl Acad Sci U S A. 1991 Oct 1;88(19):8720–8724. doi: 10.1073/pnas.88.19.8720. [DOI] [PMC free article] [PubMed] [Google Scholar]

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