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American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1999 Jan;64(1):232–249. doi: 10.1086/302204

The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs.

V Macaulay 1, M Richards 1, E Hickey 1, E Vega 1, F Cruciani 1, V Guida 1, R Scozzari 1, B Bonné-Tamir 1, B Sykes 1, A Torroni 1
PMCID: PMC1377722  PMID: 9915963

Abstract

Variation in the human mitochondrial genome (mtDNA) is now routinely described and used to infer the histories of peoples, by means of one of two procedures, namely, the assaying of RFLPs throughout the genome and the sequencing of parts of the control region (CR). Using 95 samples from the Near East and northwest Caucasus, we present an analysis based on both systems, demonstrate their concordance, and, using additional available information, present the most refined phylogeny to date of west Eurasian mtDNA. We describe and apply a nomenclature for mtDNA clusters. Hypervariable nucleotides are identified, and the relative mutation rates of the two systems are evaluated. We point out where ambiguities remain. The identification of signature mutations for each cluster leads us to apply a hierarchical scheme for determining the cluster composition of a sample of Berber speakers, previously analyzed only for CR variation. We show that the main indigenous North African cluster is a sister group to the most ancient cluster of European mtDNAs, from which it diverged approximately 50,000 years ago.

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Selected References

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  1. Anderson S., Bankier A. T., Barrell B. G., de Bruijn M. H., Coulson A. R., Drouin J., Eperon I. C., Nierlich D. P., Roe B. A., Sanger F. Sequence and organization of the human mitochondrial genome. Nature. 1981 Apr 9;290(5806):457–465. doi: 10.1038/290457a0. [DOI] [PubMed] [Google Scholar]
  2. Bandelt H. J., Forster P., Sykes B. C., Richards M. B. Mitochondrial portraits of human populations using median networks. Genetics. 1995 Oct;141(2):743–753. doi: 10.1093/genetics/141.2.743. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bendall K. E., Sykes B. C. Length heteroplasmy in the first hypervariable segment of the human mtDNA control region. Am J Hum Genet. 1995 Aug;57(2):248–256. [PMC free article] [PubMed] [Google Scholar]
  4. Calafell F., Underhill P., Tolun A., Angelicheva D., Kalaydjieva L. From Asia to Europe: mitochondrial DNA sequence variability in Bulgarians and Turks. Ann Hum Genet. 1996 Jan;60(Pt 1):35–49. doi: 10.1111/j.1469-1809.1996.tb01170.x. [DOI] [PubMed] [Google Scholar]
  5. Chen Y. S., Torroni A., Excoffier L., Santachiara-Benerecetti A. S., Wallace D. C. Analysis of mtDNA variation in African populations reveals the most ancient of all human continent-specific haplogroups. Am J Hum Genet. 1995 Jul;57(1):133–149. [PMC free article] [PubMed] [Google Scholar]
  6. Côrte-Real H. B., Macaulay V. A., Richards M. B., Hariti G., Issad M. S., Cambon-Thomsen A., Papiha S., Bertranpetit J., Sykes B. C. Genetic diversity in the Iberian Peninsula determined from mitochondrial sequence analysis. Ann Hum Genet. 1996 Jul;60(Pt 4):331–350. doi: 10.1111/j.1469-1809.1996.tb01196.x. [DOI] [PubMed] [Google Scholar]
  7. 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]
  8. Forster P., Harding R., Torroni A., Bandelt H. J. Origin and evolution of Native American mtDNA variation: a reappraisal. Am J Hum Genet. 1996 Oct;59(4):935–945. [PMC free article] [PubMed] [Google Scholar]
  9. Francalacci P., Bertranpetit J., Calafell F., Underhill P. A. Sequence diversity of the control region of mitochondrial DNA in Tuscany and its implications for the peopling of Europe. Am J Phys Anthropol. 1996 Aug;100(4):443–460. doi: 10.1002/(SICI)1096-8644(199608)100:4<443::AID-AJPA1>3.0.CO;2-S. [DOI] [PubMed] [Google Scholar]
  10. Hasegawa M., Di Rienzo A., Kocher T. D., Wilson A. C. Toward a more accurate time scale for the human mitochondrial DNA tree. J Mol Evol. 1993 Oct;37(4):347–354. doi: 10.1007/BF00178865. [DOI] [PubMed] [Google Scholar]
  11. Hofmann S., Jaksch M., Bezold R., Mertens S., Aholt S., Paprotta A., Gerbitz K. D. Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease. Hum Mol Genet. 1997 Oct;6(11):1835–1846. doi: 10.1093/hmg/6.11.1835. [DOI] [PubMed] [Google Scholar]
  12. 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]
  13. Howell N., Bogolin C., Jamieson R., Marenda D. R., Mackey D. A. mtDNA mutations that cause optic neuropathy: how do we know? Am J Hum Genet. 1998 Jan;62(1):196–202. doi: 10.1086/301675. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Howell N., Kubacka I., Halvorson S., Howell B., McCullough D. A., Mackey D. Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees. Genetics. 1995 May;140(1):285–302. doi: 10.1093/genetics/140.1.285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Krings M., Stone A., Schmitz R. W., Krainitzki H., Stoneking M., Päbo S. Neandertal DNA sequences and the origin of modern humans. Cell. 1997 Jul 11;90(1):19–30. doi: 10.1016/s0092-8674(00)80310-4. [DOI] [PubMed] [Google Scholar]
  16. Lamminen T., Huoponen K., Sistonen P., Juvonen V., Lahermo P., Aula P., Nikoskelainen E., Savontaus M. L. mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy. Eur J Hum Genet. 1997 Sep-Oct;5(5):271–279. [PubMed] [Google Scholar]
  17. Lindholm E., Cavelier L., Howell W. M., Eriksson I., Jalonen P., Adolfsson R., Blackwood D. H., Muir W. J., Brookes A. J., Gyllensten U. Mitochondrial sequence variants in patients with schizophrenia. Eur J Hum Genet. 1997 Nov-Dec;5(6):406–412. [PubMed] [Google Scholar]
  18. Ozawa T., Tanaka M., Ino H., Ohno K., Sano T., Wada Y., Yoneda M., Tanno Y., Miyatake T., Tanaka T. Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease. Biochem Biophys Res Commun. 1991 Apr 30;176(2):938–946. doi: 10.1016/s0006-291x(05)80276-1. [DOI] [PubMed] [Google Scholar]
  19. Passarino G., Semino O., Quintana-Murci L., Excoffier L., Hammer M., Santachiara-Benerecetti A. S. Different genetic components in the Ethiopian population, identified by mtDNA and Y-chromosome polymorphisms. Am J Hum Genet. 1998 Feb;62(2):420–434. doi: 10.1086/301702. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Pinto F., González A. M., Hernández M., Larruga J. M., Cabrera V. M. Genetic relationship between the Canary Islanders and their African and Spanish ancestors inferred from mitochondrial DNA sequences. Ann Hum Genet. 1996 Jul;60(Pt 4):321–330. doi: 10.1111/j.1469-1809.1996.tb01195.x. [DOI] [PubMed] [Google Scholar]
  21. Pult I., Sajantila A., Simanainen J., Georgiev O., Schaffner W., Päbo S. Mitochondrial DNA sequences from Switzerland reveal striking homogeneity of European populations. Biol Chem Hoppe Seyler. 1994 Dec;375(12):837–840. [PubMed] [Google Scholar]
  22. Richards M. B., Macaulay V. A., Bandelt H. J., Sykes B. C. Phylogeography of mitochondrial DNA in western Europe. Ann Hum Genet. 1998 May;62(Pt 3):241–260. doi: 10.1046/j.1469-1809.1998.6230241.x. [DOI] [PubMed] [Google Scholar]
  23. 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]
  24. Stoneking M., Hedgecock D., Higuchi R. G., Vigilant L., Erlich H. A. Population variation of human mtDNA control region sequences detected by enzymatic amplification and sequence-specific oligonucleotide probes. Am J Hum Genet. 1991 Feb;48(2):370–382. [PMC free article] [PubMed] [Google Scholar]
  25. Torroni A., Bandelt H. J., D'Urbano L., Lahermo P., Moral P., Sellitto D., Rengo C., Forster P., Savontaus M. L., Bonné-Tamir B. mtDNA analysis reveals a major late Paleolithic population expansion from southwestern to northeastern Europe. Am J Hum Genet. 1998 May;62(5):1137–1152. doi: 10.1086/301822. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Torroni A., Huoponen K., Francalacci P., Petrozzi M., Morelli L., Scozzari R., Obinu D., Savontaus M. L., Wallace D. C. Classification of European mtDNAs from an analysis of three European populations. Genetics. 1996 Dec;144(4):1835–1850. doi: 10.1093/genetics/144.4.1835. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Torroni A., Lott M. T., Cabell M. F., Chen Y. S., Lavergne L., Wallace D. C. mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region. Am J Hum Genet. 1994 Oct;55(4):760–776. [PMC free article] [PubMed] [Google Scholar]
  28. Torroni A., Miller J. A., Moore L. G., Zamudio S., Zhuang J., Droma T., Wallace D. C. Mitochondrial DNA analysis in Tibet: implications for the origin of the Tibetan population and its adaptation to high altitude. Am J Phys Anthropol. 1994 Feb;93(2):189–199. doi: 10.1002/ajpa.1330930204. [DOI] [PubMed] [Google Scholar]
  29. Torroni A., Petrozzi M., D'Urbano L., Sellitto D., Zeviani M., Carrara F., Carducci C., Leuzzi V., Carelli V., Barboni P. Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. Am J Hum Genet. 1997 May;60(5):1107–1121. [PMC free article] [PubMed] [Google Scholar]
  30. Torroni A., Schurr T. G., Cabell M. F., Brown M. D., Neel J. V., Larsen M., Smith D. G., Vullo C. M., Wallace D. C. Asian affinities and continental radiation of the four founding Native American mtDNAs. Am J Hum Genet. 1993 Sep;53(3):563–590. [PMC free article] [PubMed] [Google Scholar]
  31. Wakeley J. Substitution rate variation among sites in hypervariable region 1 of human mitochondrial DNA. J Mol Evol. 1993 Dec;37(6):613–623. doi: 10.1007/BF00182747. [DOI] [PubMed] [Google Scholar]
  32. Watson E., Forster P., Richards M., Bandelt H. J. Mitochondrial footprints of human expansions in Africa. Am J Hum Genet. 1997 Sep;61(3):691–704. doi: 10.1086/515503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Wilkinson-Herbots H. M., Richards M. B., Forster P., Sykes B. C. Site 73 in hypervariable region II of the human mitochondrial genome and the origin of European populations. Ann Hum Genet. 1996 Nov;60(Pt 6):499–508. doi: 10.1111/j.1469-1809.1996.tb01616.x. [DOI] [PubMed] [Google Scholar]

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