Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Review Article
  • Published:

Reconstructing human origins in the genomic era

Key Points

  • Over the past two decades, phylogenetic analyses of mitochondrial DNA and Y-chromosome polymorphisms supported a simple model of human origins, called the single origin hypothesis.

  • The single origin model proposes that anatomically modern humans trace their ancestry to a single small population that lived in Africa, and that, following a speciation bottleneck, the population expanded and completely replaced archaic forms of humans.

  • More sophisticated methods of analysis, based on the coalescent approach, are being applied to a plethora of new genomic sequence data.

  • These new analyses of multilocus sequence data show a large variance in the shape and depth of genealogies for X-chromosomal and autosomal loci, and present a more complex picture of human demographic history.

  • Non-African populations have reduced diversity and fewer rare polymorphisms than African populations, suggesting a history of bottlenecks. By contrast, African populations do not exhibit the predicted patterns of polymorphism after a speciation bottleneck.

  • These genome-scale patterns could be best accounted for by models that involve low levels of gene flow among archaic populations before the emergence of anatomically modern humans — that is, they imply the existence of ancestral population structure.

  • There is also growing evidence that some highly divergent genetic lineages might have entered our genome through hybridization between an expanding anatomically modern human population and archaic forms of humans.

  • Further tests of the predictions of these models await more systematic surveys of DNA sequence variation in multiple human populations, along with more sophisticated methods of population genetic inference.

Abstract

Analyses of recently acquired genomic sequence data are leading to important insights into the early evolution of anatomically modern humans, as well as into the more recent demographic processes that accompanied the global radiation of Homo sapiens. Some of the new results contradict early, but still influential, conclusions that were based on analyses of gene trees from mitochondrial DNA and Y-chromosome sequences. In this review, we discuss the different genetic and statistical methods that are available for studying human population history, and identify the most plausible models of human evolution that can accommodate the contrasting patterns observed at different loci throughout the genome.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Frequency distribution of Tajima's D.
Figure 2: Frequency distribution of times to the most recent common ancestor (TMRCA).
Figure 3: Time to most recent common ancestor and hominin fossil dates.
Figure 4: Models of human origins.

Similar content being viewed by others

References

  1. Day, M. H. Omo human skeletal remains. Nature 222, 1135–1138 (1969).

    Article  CAS  PubMed  Google Scholar 

  2. McDougall, I., Brown, F. H. & Fleagle, J. G. Stratigraphic placement and age of modern humans from Kibish, Ethiopia. Nature 433, 733–736 (2005).

    Article  CAS  PubMed  Google Scholar 

  3. Wood, B. Hominid revelations from Chad. Nature 418, 133–135 (2002).

    Article  CAS  PubMed  Google Scholar 

  4. Anton, S. C. & Swisher, C. C. Early dispersal of Homo from Africa. Annu. Rev. Anthropol. 33, 271–296 (2004).

    Article  Google Scholar 

  5. Teshima, K. M., Coop, G. & Przeworski, M. How reliable are empirical genomic scans for selective sweeps? Genome Res. 16, 702–712 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Stringer, C. B. & Andrews, P. Genetic and fossil evidence for the origin of modern humans. Science 239, 1263–1268 (1988). An early synthesis of genetic and fossil evidence that supports the recent African origin of anatomically modern humans.

    Article  CAS  PubMed  Google Scholar 

  7. Cann, R. L., Stoneking, M. & Wilson, A. C. Mitochondrial DNA and human evolution. Nature 325, 31–36 (1987). An influential paper that discusses one of the first attempts to use mtDNA data to infer the origin of anatomically modern humans.

    Article  CAS  PubMed  Google Scholar 

  8. Excoffier, L. Human demographic history: refining the recent African origin model. Curr. Opin. Genet. Dev. 12, 675–682 (2002).

    Article  CAS  PubMed  Google Scholar 

  9. Harpending, H. C. et al. Genetic traces of ancient demography. Proc. Natl Acad. Sci. USA 95, 1961–1967 (1998). One of the first comparisons of haploid and non-haploid sequence data in the context of explicit models that incorporate a history of bottlenecks and different ancestral effective population sizes for modern humans.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Cavalli-Sforza, L. L., Menozzi, P. & Piazza, A. The History and Geography of Human Genes (Princeton Univ. Press, Princeton, New Jersey, 1994).

    Google Scholar 

  11. Cavalli-Sforza, L. L. & Feldman, M. W. The application of molecular genetic approaches to the study of human evolution. Nature Genet. 33, S266–S275 (2003).

    Article  CAS  Google Scholar 

  12. Hey, J. & Machado, C. A. The study of structured populations — new hope for a difficult and divided science. Nature Rev. Genet. 4, 535–543 (2003).

    Article  CAS  PubMed  Google Scholar 

  13. Avise, J. C. et al. Intraspecific phylogeography: the mitochondrial bridge between population genetics and systematics. Annu. Rev. Ecol. Syst. 18, 489–522 (1987).

    Article  Google Scholar 

  14. Vigilant, L., Stoneking, M., Harpending, H., Hawkes, K. & Wilson, A. C. African populations and the evolution of human mitochondrial DNA. Science 253, 1503–1507 (1991).

    Article  CAS  PubMed  Google Scholar 

  15. Ingman, M., Kaessmann, H., Pääbo, S. & Gyllensten, U. Mitochondrial genome variation and the origin of modern humans. Nature 408, 708–713 (2000).

    Article  CAS  PubMed  Google Scholar 

  16. Hammer, M. F. et al. Out of Africa and back again: nested cladistic analysis of human Y chromosome variation. Mol. Biol. Evol. 15, 427–441 (1998).

    Article  CAS  PubMed  Google Scholar 

  17. Underhill, P. A. et al. Y chromosome sequence variation and the history of human populations. Nature Genet. 26, 358–361 (2000).

    Article  CAS  PubMed  Google Scholar 

  18. Takahata, N., Lee, S. H. & Satta, Y. Testing multiregionality of modern human origins. Mol. Biol. Evol. 18, 172–183 (2001).

    Article  CAS  PubMed  Google Scholar 

  19. Garrigan, D., Mobasher, Z., Severson, T., Wilder, J. A. & Hammer, M. F. Evidence for archaic Asian ancestry on the human X chromosome. Mol. Biol. Evol. 22, 189–192 (2005).

    Article  CAS  PubMed  Google Scholar 

  20. Wilder, J. A., Mobasher, Z. & Hammer, M. F. Genetic evidence for unequal effective population sizes of human females and males. Mol. Biol. Evol. 21, 2047–2057 (2004).

    Article  CAS  PubMed  Google Scholar 

  21. Jaruzelska, J., Zietkiewicz, E. & Labuda, D. Is selection responsible for the low level of variation in the last intron of the ZFY locus? Mol. Biol. Evol. 16, 1633–1640 (1999).

    Article  CAS  PubMed  Google Scholar 

  22. Harding, R. M. & McVean, G. A structured ancestral population for the evolution of modern humans. Curr. Opin. Genet. Dev. 14, 667–674 (2004).

    Article  CAS  PubMed  Google Scholar 

  23. Watterson, G. A. On the number of segregating sites in genetical models without recombination. Theor. Popul. Biol. 7, 256–276 (1975).

    Article  CAS  PubMed  Google Scholar 

  24. Tajima, F. Evolutionary relationship of DNA sequences in finite populations. Genetics 105, 437–460 (1983).

    CAS  PubMed  PubMed Central  Google Scholar 

  25. Hammer, M. F. et al. Heterogeneous patterns of variation among multiple human X-linked loci: the possible role of diversity-reducing selection in non-Africans. Genetics 167, 1841–1853 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Harding, R. M. et al. Archaic African and Asian lineages in the genetic ancestry of modern humans. Am. J. Hum. Genet. 60, 772–789 (1997). A seminal paper on the use of autosomal resequencing data to infer the history of modern human populations.

    CAS  PubMed  PubMed Central  Google Scholar 

  27. Zhao, Z. et al. Worldwide DNA sequence variation in a 10-kilobase noncoding region on human chromosome 22. Proc. Natl Acad. Sci. USA 97, 11354–11358. (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Yu, N. et al. Global patterns of human DNA sequence variation in a 10-kb region on chromosome 1. Mol. Biol. Evol. 18, 214–222 (2001).

    Article  CAS  PubMed  Google Scholar 

  29. Fischer, A., Wiebe, V., Pääbo, S. & Przeworski, M. Evidence for a complex demographic history of chimpanzees. Mol. Biol. Evol. 21, 799–808 (2004).

    Article  CAS  PubMed  Google Scholar 

  30. Yu, N. et al. Low nucleotide diversity in chimpanzees and bonobos. Genetics 164, 1511–1518 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  31. Kaessmann, H., Wiebe, V., Weiss, G. & Pääbo, S. Great ape DNA sequences reveal a reduced diversity and an expansion in humans. Nature Genet. 27, 155–156 (2001).

    Article  CAS  PubMed  Google Scholar 

  32. Tajima, F. The effect of change in population size on DNA polymorphism. Genetics 123, 597–601 (1989).

    CAS  PubMed  PubMed Central  Google Scholar 

  33. Fu, Y. X. & Li, W. H. Statistical tests of neutrality of mutations. Genetics 133, 693–709 (1993).

    CAS  PubMed  PubMed Central  Google Scholar 

  34. Fay, J. C. & Wu, C. I. A human population bottleneck can account for the discordance between patterns of mitochondrial versus nuclear DNA variation. Mol. Biol. Evol. 16, 1003–1005 (1999). The first paper to recognize that differences in the effective population sizes of the haploid and autosomal compartments of the genome result in a different frequency spectrum after a population bottleneck.

    Article  CAS  PubMed  Google Scholar 

  35. Charlesworth, B., Charlesworth, D. & Barton, D. E. The effects of genetic and geographic structure on neutral variation. Annu. Rev. Ecol. Syst. 34, 99–125 (2003).

    Article  Google Scholar 

  36. Hammer, M., Blackmer, F., Garrigan, D., Nachman, M. & Wilder, J. Human population structure and its effects on sampling Y chromosome variation. Genetics 164, 1495–1509 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  37. Ptak, S. E. & Przeworski, M. Evidence for population growth in humans is confounded by fine-scale population structure. Trends Genet. 18, 559–563 (2002).

    Article  PubMed  Google Scholar 

  38. Kingman, J. F. C. On the genealogy of a large population. J. Appl. Probab. 19A, 27–43 (1982).

    Article  Google Scholar 

  39. Kingman, J. F. C. The coalescent. Stochastic Process Appl. 13, 235–248 (1982).

    Article  Google Scholar 

  40. Stephens, M. & Donnelly, P. Inference in molecular population genetics. J. R. Stat. Soc. Ser. B 62, 605–655 (2000).

    Article  Google Scholar 

  41. Beaumont, M. A. Recent developments in genetic data analysis: what can they tell us about human demographic history? Heredity 92, 365–379 (2004).

    Article  CAS  PubMed  Google Scholar 

  42. Tavare, S., Balding, D. J., Griffiths, R. C. & Donnelly, P. Inferring coalescence times from DNA sequence data. Genetics 145, 505–518 (1997). Presents for the first time the argument that the likelihood of an evolutionary model can be calculated from a statistical summary of genetic data, rather than directly from the data.

    CAS  PubMed  PubMed Central  Google Scholar 

  43. Pritchard, J. K., Seielstad, M. T., Perez-Lezaun, A. & Feldman, M. W. Population growth of human Y chromosomes: a study of Y chromosome microsatellites. Mol. Biol. Evol. 16, 1791–1798 (1999).

    Article  CAS  PubMed  Google Scholar 

  44. Voight, B. F. et al. Interrogating multiple aspects of variation in a full resequencing data set to infer human population size changes. Proc. Natl Acad. Sci. USA 102, 18508–18513 (2005). A recent study of 50 non-coding resequenced loci that supports a strong genetic bottleneck as humans migrated from Africa.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  45. Wall, J. D. & Przeworski, M. When did the human population size start increasing? Genetics 155, 1865–1874 (2000). Among the first analyses to acknowledge that there is too much variance in the genomic frequency spectrum to be compatible with any simple neutral model of population history.

    CAS  PubMed  PubMed Central  Google Scholar 

  46. Slatkin, M. & Hudson, R. R. Pairwise comparisons of mitochondrial DNA sequences in stable and exponentially growing populations. Genetics 129, 555–562 (1991).

    CAS  PubMed  PubMed Central  Google Scholar 

  47. Di Rienzo, A. & Wilson, A. C. Branching pattern in the evolutionary tree for human mitochondrial DNA. Proc. Natl Acad. Sci. USA 88, 1597–1601 (1991).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Rogers, A. R. Genetic evidence for a Pleistocene population explosion. Evolution 49, 608–615 (1995).

    Article  PubMed  Google Scholar 

  49. Hey, J. Mitochondrial and nuclear genes present conflicting portraits of human origins. Mol. Biol. Evol. 14, 166–172 (1997).

    Article  CAS  PubMed  Google Scholar 

  50. Przeworski, M., Hudson, R. R. & Di Rienzo, A. Adjusting the focus on human variation. Trends Genet. 16, 296–302 (2000).

    Article  CAS  PubMed  Google Scholar 

  51. Frisse, L. et al. Gene conversion and different population histories may explain the contrast between polymorphism and linkage disequilibrium levels. Am. J. Hum. Genet. 69, 831–843 (2001).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Harpending, H. & Rogers, A. Genetic perspectives on human origins and differentiation. Annu. Rev. Genomics Hum. Genet. 1, 361–385 (2000).

    Article  CAS  PubMed  Google Scholar 

  53. Adams, A. M. & Hudson, R. R. Maximum-likelihood estimation of demographic parameters using the frequency spectrum of unlinked single-nucleotide polymorphisms. Genetics 168, 1699–1712 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. Marth, G. T., Czabarka, E., Murvai, J. & Sherry, S. T. The allele frequency spectrum in genome-wide human variation data reveals signals of differential demographic history in three large world populations. Genetics 166, 351–372 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Reich, D. E. et al. Linkage disequilibrium in the human genome. Nature 411, 199–204 (2001).

    Article  CAS  PubMed  Google Scholar 

  56. Akey, J. M. et al. Population history and natural selection shape patterns of genetic variation in 132 genes. PLoS Biol. 2, e286 (2004).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  57. Pluzhnikov, A., Di Rienzo, A. & Hudson, R. R. Inferences about human demography based on multilocus analyses of noncoding sequences. Genetics 161, 1209–1218 (2002).

    PubMed  PubMed Central  Google Scholar 

  58. InternationalHapMapConsortium. A haplotype map of the human genome. Nature 437, 1299–1320 (2005).

  59. Lonjou, C. et al. Linkage disequilibrium in human populations. Proc. Natl Acad. Sci. USA 100, 6069–6074 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Wakeley, J. & Aliacar, N. Gene genealogies in a metapopulation. Genetics 159, 893–905 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  61. Klein, R. G. The Human Career: Human Biological and Cultural Origins (Univ. Chicago Press, Chicago, 1999).

    Google Scholar 

  62. Wakeley, J., Nielsen, R., Liu-Cordero, S. N. & Ardlie, K. The discovery of single-nucleotide polymorphisms and inferences about human demographic history. Am. J. Hum. Genet. 69, 1332–1347 (2001).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Satta, Y. & Takahata, N. The distribution of the ancestral haplotype in finite stepping-stone models with population expansion. Mol. Ecol. 13, 877–886 (2004).

    Article  CAS  PubMed  Google Scholar 

  64. Templeton, A. R. Out of Africa again and again. Nature 416, 45–51 (2002).

    Article  CAS  PubMed  Google Scholar 

  65. Zietkiewicz, E. et al. Haplotypes in the dystrophin DNA segment point to a mosaic origin of modern human diversity. Am. J. Hum. Genet. 73, 994–1015 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  66. Harris, E. E. & Hey, J. X chromosome evidence for ancient human histories. Proc. Natl Acad. Sci. USA 96, 3320–3324 (1999). One of the first papers to show the effects of ancient population structure on patterns of polymorphism at a locus in humans.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  67. Garrigan, D., Mobasher, Z., Kingan, S. B., Wilder, J. A. & Hammer, M. F. Deep haplotype divergence and long-range linkage disequilibrium at Xp21.1 provide evidence that humans descend from a structured ancestral population. Genetics 170, 1849–1856 (2005). The first resequencing data set to reject the hypothesis that humans are descended from a single, randomly mating ancestral population.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Baird, D. M., Coleman, J., Rosser, Z. H. & Royle, N. J. High levels of sequence polymorphism and linkage disequilibrium at the telomere of 12q: implications for telomere biology and human evolution. Am. J. Hum. Genet. 66, 235–250 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  69. Barreiro, L. B. et al. The heritage of pathogen pressures and ancient demography in the human innate-immunity CD209/CD209L region. Am. J. Hum. Genet. 77, 869–886 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  70. Hardy, J. et al. Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiens. Biochem. Soc. Trans 33, 582–585 (2005).

    Article  CAS  PubMed  Google Scholar 

  71. Stefansson, H. et al. A common inversion under selection in Europeans. Nature Genet. 37, 129–137 (2005).

    Article  CAS  PubMed  Google Scholar 

  72. Hayakawa, T., Aki, I., Varki, A., Satta, Y. & Takahata, N. Fixation of the human-specific CMP-N-acetylneuraminic acid hydroxylase pseudogene and implications of haplotype diversity for human evolution. Genetics 172, 1139–1146 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  73. Koda, Y. et al. Contrasting patterns of polymorphisms at the ABO-secretor gene (FUT2) and plasma α(1,3)fucosyltransferase gene (FUT6) in human populations. Genetics 158, 747–756 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  74. Wolpoff, M. H. Paleoanthropology (McGraw-Hil, Boston, 1999).

    Google Scholar 

  75. Stringer, C. Human evolution: out of Ethiopia. Nature 423, 692–693 (2003).

    Article  CAS  PubMed  Google Scholar 

  76. Brauer, G. in The Human Revolution: Behavioural and Biological Perspectives on the Origins of Modern Humans (eds Mellars, P. & Stringer, C.) 123–154 (Edinburgh Univ. Press, Edinburgh, 1989).

    Google Scholar 

  77. Smith, F. H., Jankovic, I. & Karavanic, I. The assimilation model, human origins in Europe, and the extinction of Neanderthals. Quaternary Int. 137, 7–19 (2005).

    Article  Google Scholar 

  78. Eswaran, V. A diffusion wave out of Africa: the mechanism of the modern human revolution? Curr. Anthropol. 43, 749–774 (2002).

    Article  Google Scholar 

  79. Relethford, J. Genetics and the Search for Modern Human Origins (Wiley-Liss, New York, 2001).

    Google Scholar 

  80. Plagnol, V. & Wall, J. D. Possible ancestral structure in human populations. PLoS Genet. 2, e105 (2006).

    Article  PubMed  PubMed Central  Google Scholar 

  81. Pääbo, S. The mosaic that is our genome. Nature 421, 409–412 (2003).

    Article  PubMed  CAS  Google Scholar 

  82. Wilder, J. A., Kingan, S. B., Mobasher, Z., Pilkington, M. M. & Hammer, M. F. Global patterns of human mitochondrial DNA and Y-chromosome structure are not influenced by higher migration rates of females versus males. Nature Genet. 36, 1122–1125 (2004).

    Article  CAS  PubMed  Google Scholar 

  83. Kitano, T., Schwarz, C., Nickel, B. & Pääbo, S. Gene diversity patterns at 10 X-chromosomal loci in humans and chimpanzees. Mol. Biol. Evol. 20, 1281–1289 (2003).

    Article  CAS  PubMed  Google Scholar 

  84. Alonso, S. & Armour, J. A. A highly variable segment of human subterminal 16p reveals a history of population growth for modern humans outstide Africa. Proc. Natl Acad. Sci. USA 98, 864–869 (2001).

    Article  CAS  PubMed  Google Scholar 

  85. Martinez-Arias, R. et al. Sequence variability of a human pseudogene. Genome Res. 11, 1071–1085 (2001).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  86. Rieder, M. J., Taylor, S. L., Clark, A. G. & Nickerson, D. A. Sequence variation in the human angiotensin converting enzyme. Nature Genet. 22, 59–62 (1999).

    Article  CAS  PubMed  Google Scholar 

  87. Clark, A. G. et al. Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase. Am. J. Hum. Genet. 63, 595–612 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  88. Fullerton, S. M. et al. Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism. Am. J. Hum. Genet. 67, 881–900 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  89. Bamshad, M. J. et al. A strong signature of balancing selection in the 5′ cis-regulatory region of CCR5. Proc. Natl Acad. Sci. USA 99, 10539–10544 (2002).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  90. Wooding, S. P. et al. DNA sequence variation in a 3.7-kb noncoding sequence 5′ of the CYP1A2 gene: implications for human population history and natural selection. Am. J. Hum. Genet. 71, 528–542 (2002).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  91. Toomajian, C. & Kreitman, M. Sequence variation and haplotype structure at the human HFE locus. Genetics 161, 1609–1623 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  92. Harding, R. M. et al. Evidence for variable selective pressures at MC1R. Am. J. Hum. Genet. 66, 1351–1361 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  93. Harris, E. E. & Hey, J. Human populations show reduced DNA sequence variation at the factor IX locus. Curr. Biol. 11, 774–778 (2001).

    Article  CAS  PubMed  Google Scholar 

  94. Alonso, S. & Armour, J. A. Compound haplotypes at Xp11.23 and human population growth in Eurasia. Ann. Hum. Genet. 68, 428–437 (2004).

    Article  CAS  PubMed  Google Scholar 

  95. Templeton, A. R. Haplotype trees and modern human origins. Yearb. Phys. Anthropol. 48, 33–59 (2005).

    Article  Google Scholar 

  96. Patin, E. et al. Deciphering the ancient and complex evolutionary history of human arylamine N-acetyltransferase genes. Am. J. Hum. Genet. 78, 423–436 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  97. Vander Molen, J. et al. Population genetics of CAPN10 and GPR35: implications for the evolution of type 2 diabetes variants. Am. J. Hum. Genet. 76, 548–560 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We thank A. Di Rienzo for providing Tajima's D values and the following people for providing feedback on the manuscript: M. Cox, L. Excoffier, F. Mendez, C. Stringer, J. Wilder and E. Wood. Some of the work presented here was made possible by a US National Science Foundation HOMINID grant to M.F.H.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Michael F. Hammer.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Related links

Related links

FURTHER INFORMATION

Michael Hammer's laboratory homepage

Glossary

Hominin

All the taxa on the human lineage after the split from the common ancestor with the chimpanzee.

Neutral DNA polymorphism

Nucleotide variants that segregate in a population but have frequencies that are not influenced by natural selection.

Demographic processes

Changes in population size, distribution and structure.

Bottleneck

A transient reduction in the abundance of a population. This could occur, for example, because of environmental catastrophe or after the founding of a new population.

Pleistocene

An epoch of the Quaternary period beginning 1.8 million years ago and transitioning to the Holocene epoch approximately 10,000 years ago. The Pleistocene is characterized by a cool climate and extensive glaciation of northern latitudes.

Population phylogeny

The hierarchical relationship among individual populations, typically inferred from pairwise genetic differences between populations.

Summary statistics

Statistics that describe some aspect of polymorphism data, such as the number of polymorphic sites, the distribution of mutation frequencies or the extent of association between linked polymorphisms. Summary statistics are often estimates of parameters in an evolutionary model.

Coalescent approach

A probabilistic construct that describes the hierarchical common ancestry of a sample of gene copies. The probability that two gene copies share a common ancestor (or coalesce) in the preceding generation is proportional to the reciprocal of the size of the entire population.

Haplotype

A contiguous DNA sequence of arbitrary length along a chromosome that has a primary structure that is distinct from that of other homologous regions in a given population.

Place of the most recent common ancestor

The geographical area, of arbitrary scale, where the ancestry of a current sample of gene copies can be traced back to a single, endemic ancestral population.

Derived

The state of genotypic or phenotypic character, possessed by some biological entity, which has mutated from a common ancestral state.

Paraphyletic

When the common ancestor of one natural group is shared with any other such group.

Time to the most recent common ancestor

The number of generations back in time when a single gene copy gave rise to all of the gene copies in a contemporary sample. If n gene copies are sampled from a population of size N, the time to a most recent common ancestor for an autosomal locus is expected to be 4N(1 − 1/n) generations.

Effective population size

The number of individuals of a given generation that contribute gametes to the subsequent generations. This abstract quantity depends on the breeding sex ratio, number of offspring per individual and type of mating system.

Island model of population structure

A commonly used model to describe gene flow in a subdivided population in which each subpopulation of constant size, N, receives and gives migrants to each of the other subpopulations at the same rate, m. Under the Island model, FST = 1/(4Nm + 1).

Standard neutral model

A population genetics model that assumes all individuals in a population are replaced by their offspring each generation, so that the population size remains constant, mating occurs randomly and each parent produces a Poisson-distributed number of offspring. Under these conditions, the model predicts the fate of mutations that are not affected by natural selection.

Harmonic mean

One method for calculating an average, defined as the reciprocal of the arithmetic mean of the reciprocals of a specified set of positive numbers.

Tajima's D

A statistic used to test the standard neutral model for a given region of DNA sequence. It is the standardized difference between the number of pairwise nucleotide differences and the total number of segregating sites.

Frequency spectrum

The distribution of polymorphism frequencies in a sample of DNA sequences. For example, 30% of polymorphisms might occur in a single gene copy, 20% in two gene copies, and so on. Under the standard neutral model, the frequency spectrum is expected to follow a geometric distribution.

Linkage disequilibrium

The non-random association of polymorphisms at two linked loci. Linkage disequilibrium is created by mutation, but broken down over time primarily by crossing over between the two loci.

Directional selection

A form of positive selection in which a single mutation has a selective advantage over all other mutations, resulting in the selected mutation rapidly reaching fixation (that is, a frequency of 100%) in the population.

Balancing selection

A form of positive selection that maintains polymorphism in the population. One well-known form of balancing selection is heterozygote advantage, where an individual who is heterozygous at a selected locus has a higher fitness than either of the homozygous genotypes.

Population structure

Arises when the individual members of a population do not mate at random with respect to geography, age class, language, culture or some other defining characteristic.

Likelihood-based method

A class of statistical methods that calculate the probability of the observed data under varying hypotheses, in order to estimate model parameters that best explain the observed data and determine the relative strengths of alternative hypotheses.

Bayesian technique

An approach to inference in which probability distributions of model parameters represent both what we believe about the distributions before looking at data and the likelihood of the parameters given the observed data.

Markov chain Monte Carlo technique

A simulation technique for producing samples from an unknown probability distribution. By evaluating the probability of the observed data at each step in the Markov chain, an estimate of the probability distribution of model parameters can be obtained by observing the behaviour of the chain as it proceeds through many steps.

Importance sampling

An efficient simulation method for integrating an unknown function, in which only those parameters that can actually produce the observed data are considered.

Approximate likelihood

A measure of the fit of some hypothetical model to a statistic calculated from observed data. For example, if 50% of polymorphisms occur in single individual chromosomes, a population growth model might have a higher likelihood of producing the observed number of singleton mutations than a model of population reduction.

Deme

A geographically localized population of a species that can be considered a distinct, interbreeding unit.

Neolithic

A human cultural period, beginning approximately 10,000 years ago, marked by the appearance in the archaeological record of industries such as polished stone and metal tools, pottery, animal domestication and agriculture.

Panmictic

Describes a diploid population in which each individual of a particular sex has an equal chance of producing offspring with any other member of the opposite sex in the population.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Garrigan, D., Hammer, M. Reconstructing human origins in the genomic era. Nat Rev Genet 7, 669–680 (2006). https://doi.org/10.1038/nrg1941

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1038/nrg1941

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing