Natural selection shaped regional mtDNA variation in humans

Human mtDNA shows striking regional variation, traditionally attributed to genetic drift. However, it is not easy to account for the fact that only two mtDNA lineages (M and N) left Africa to colonize Eurasia and that lineages A, C, D, and G show a 5-fold enrichment from central Asia to Siberia. As an alternative to drift, natural selection might have enriched for certain mtDNA lineages as people migrated north into colder climates. To test this hypothesis we analyzed 104 complete mtDNA sequences from all global regions and lineages. African mtDNA variation did not significantly deviate from the standard neutral model, but European, Asian, and Siberian plus Native American variations did. Analysis of amino acid substitution mutations (nonsynonymous, Ka) versus neutral mutations (synonymous, Ks) (ka/ks) for all 13 mtDNA protein-coding genes revealed that the ATP6 gene had the highest amino acid sequence variation of any human mtDNA gene, even though ATP6 is one of the more conserved mtDNA proteins. Comparison of the ka/ks ratios for each mtDNA gene from the tropical, temperate, and arctic zones revealed that ATP6 was highly variable in the mtDNAs from the arctic zone, cytochrome b was particularly variable in the temperate zone, and cytochrome oxidase I was notably more variable in the tropics. Moreover, multiple amino acid changes found in ATP6, cytochrome b, and cytochrome oxidase I appeared to be functionally significant. From these analyses we conclude that selection may have played a role in shaping human regional mtDNA variation and that one of the selective influences was climate.

[1]  F. Sanger,et al.  Sequence and organization of the human mitochondrial genome , 1981, Nature.

[2]  R. Leakey,et al.  The Origin Of Humankind , 1982 .

[3]  M. Nei,et al.  Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions. , 1986, Molecular biology and evolution.

[4]  M. Stoneking,et al.  Mitochondrial DNA and human evolution , 1987, Nature.

[5]  D. Wallace,et al.  cDNA sequence of a human skeletal muscle ADP/ATP translocator: lack of a leader peptide, divergence from a fibroblast translocator cDNA, and coevolution with mitochondrial DNA genes. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[6]  F. Tajima Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. , 1989, Genetics.

[7]  H. Harpending,et al.  Population growth makes waves in the distribution of pairwise genetic differences. , 1992, Molecular biology and evolution.

[8]  B. Crain,et al.  Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients. , 1993, Genomics.

[9]  W. Li,et al.  Statistical tests of neutrality of mutations. , 1993, Genetics.

[10]  D. Wallace,et al.  Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[11]  L. Moore,et al.  Mitochondrial DNA analysis in Tibet: implications for the origin of the Tibetan population and its adaptation to high altitude. , 1994, American journal of physical anthropology.

[12]  N. Takahata,et al.  Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[13]  D. Wallace,et al.  Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage. , 1997, American journal of human genetics.

[14]  Ziheng Yang,et al.  PAML: a program package for phylogenetic analysis by maximum likelihood , 1997, Comput. Appl. Biosci..

[15]  H. Bandelt,et al.  mtDNA analysis reveals a major late Paleolithic population expansion from southwestern to northeastern Europe. , 1998, American journal of human genetics.

[16]  C. Groves,et al.  Toward a phylogenetic classification of Primates based on DNA evidence complemented by fossil evidence. , 1998, Molecular phylogenetics and evolution.

[17]  H. Bandelt,et al.  Genetic evidence of an early exit of Homo sapiens sapiens from Africa through eastern Africa , 1999, Nature Genetics.

[18]  R. Sukernik,et al.  Mitochondrial DNA variation in Koryaks and Itel'men: population replacement in the Okhotsk Sea-Bering Sea region during the Neolithic. , 1999, American journal of physical anthropology.

[19]  D. Turnbull,et al.  Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA , 1999, Nature Genetics.

[20]  D. Wallace,et al.  Mitochondrial DNA variation in human evolution and disease. , 1999, Gene.

[21]  Julio Rozas,et al.  DnaSP version 3: an integrated program for molecular population genetics and molecular evolution analysis , 1999, Bioinform..

[22]  E. Ruiz-Pesini,et al.  Human mtDNA haplogroups associated with high or reduced spermatozoa motility. , 2000, American journal of human genetics.

[23]  S. Pääbo,et al.  Mitochondrial genome variation and the origin of modern humans , 2000, Nature.

[24]  D. Wallace,et al.  mtDNA variation in the South African Kung and Khwe-and their genetic relationships to other African populations. , 2000, American journal of human genetics.

[25]  C. Gissi,et al.  Evolution of the mitochondrial genetic system: an overview. , 2000, Gene.

[26]  G. Valle,et al.  Do the four clades of the mtDNA haplogroup L2 evolve at different rates? , 2001, American journal of human genetics.

[27]  N. Newman,et al.  Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families , 2001, Human Genetics.

[28]  C. Franceschi,et al.  Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenarians , 2001, European Journal of Human Genetics.

[29]  D. Wallace,et al.  Mitochondrial DNA Diversity in Southeast Asian Populations , 2002, Human biology.

[30]  W. Leonard,et al.  Climatic influences on basal metabolic rates among circumpolar populations , 2002, American journal of human biology : the official journal of the Human Biology Council.

[31]  D. Wallace,et al.  Sequence analysis of cDNAs for the human and bovine ATP synthase β subunit: mitochondrial DNA genes sustain seventeen times more mutations , 1987, Current Genetics.