#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Complex Patterns of Genomic Admixture within Southern Africa


Within-population genetic diversity is greatest within Africa, while between-population genetic diversity is directly proportional to geographic distance. The most divergent contemporary human populations include the click-speaking forager peoples of southern Africa, broadly defined as Khoesan. Both intra- (Bantu expansion) and inter-continental migration (European-driven colonization) have resulted in complex patterns of admixture between ancient geographically isolated Khoesan and more recently diverged populations. Using gender-specific analysis and almost 1 million autosomal markers, we determine the significance of estimated ancestral contributions that have shaped five contemporary southern African populations in a cohort of 103 individuals. Limited by lack of available data for homogenous Khoesan representation, we identify the Ju/'hoan (n = 19) as a distinct early diverging human lineage with little to no significant non-Khoesan contribution. In contrast to the Ju/'hoan, we identify ancient signatures of Khoesan and Bantu unions resulting in significant Khoesan- and Bantu-derived contributions to the Southern Bantu amaXhosa (n = 15) and Khoesan !Xun (n = 14), respectively. Our data further suggests that contemporary !Xun represent distinct Khoesan prehistories. Khoesan assimilation with European settlement at the most southern tip of Africa resulted in significant ancestral Khoesan contributions to the Coloured (n = 25) and Baster (n = 30) populations. The latter populations were further impacted by 170 years of East Indian slave trade and intra-continental migrations resulting in a complex pattern of genetic variation (admixture). The populations of southern Africa provide a unique opportunity to investigate the genomic variability from some of the oldest human lineages to the implications of complex admixture patterns including ancient and recently diverged human lineages.


Vyšlo v časopise: Complex Patterns of Genomic Admixture within Southern Africa. PLoS Genet 9(3): e32767. doi:10.1371/journal.pgen.1003309
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1003309

Souhrn

Within-population genetic diversity is greatest within Africa, while between-population genetic diversity is directly proportional to geographic distance. The most divergent contemporary human populations include the click-speaking forager peoples of southern Africa, broadly defined as Khoesan. Both intra- (Bantu expansion) and inter-continental migration (European-driven colonization) have resulted in complex patterns of admixture between ancient geographically isolated Khoesan and more recently diverged populations. Using gender-specific analysis and almost 1 million autosomal markers, we determine the significance of estimated ancestral contributions that have shaped five contemporary southern African populations in a cohort of 103 individuals. Limited by lack of available data for homogenous Khoesan representation, we identify the Ju/'hoan (n = 19) as a distinct early diverging human lineage with little to no significant non-Khoesan contribution. In contrast to the Ju/'hoan, we identify ancient signatures of Khoesan and Bantu unions resulting in significant Khoesan- and Bantu-derived contributions to the Southern Bantu amaXhosa (n = 15) and Khoesan !Xun (n = 14), respectively. Our data further suggests that contemporary !Xun represent distinct Khoesan prehistories. Khoesan assimilation with European settlement at the most southern tip of Africa resulted in significant ancestral Khoesan contributions to the Coloured (n = 25) and Baster (n = 30) populations. The latter populations were further impacted by 170 years of East Indian slave trade and intra-continental migrations resulting in a complex pattern of genetic variation (admixture). The populations of southern Africa provide a unique opportunity to investigate the genomic variability from some of the oldest human lineages to the implications of complex admixture patterns including ancient and recently diverged human lineages.


Zdroje

1. IngmanM, KaessmannH, PääboS, GyllenstenU (2000) Mitochondrial genome variation and the origin of modern humans. Nature 408: 708–713.

2. LiJZ, AbsherDM, TangH, SouthwickAM, CastoAM, et al. (2008) Worldwide human relationships inferred from genome-wide patterns of variation. Science 319: 1100–1104.

3. TishkoffSA, ReedFA, FriedlaenderFR, EhretC, RanciaroA, et al. (2009) The genetic structure and history of Africans and African Americans. Science 324: 1035–1044.

4. HennBM, GignouxCR, JobinM, GrankaJM, MacphersonJM, et al. (2011) Hunter-gatherer genomic diversity suggests a southern African origin for modern humans. Proc Natl Acad Sci U S A 108: 5154–5162.

5. SchusterSC, MillerW, RatanA, TomshoLP, GiardineB, et al. (2010) Complete Khoisan and Bantu genomes from southern Africa. Nature 463: 943–947.

6. GronauI, HubiszMJ, GulkoB, DankoCG, SiepelA (2011) Bayesian inference of ancient human demography from individual genome sequences. Nat Genet 43: 1031–1034.

7. Berniell-LeeG, CalafellF, BoschE, HeyerE, SicaL, et al. (2009) Genetic and demographic implications of the Bantu expansion: insights from human paternal lineages. Mol Biol Evol 26: 1581–1589.

8. Newman JL. (1995) The Peopling of Africa: A Geographic Interpretation. Yale University Press

9. van der Ross RE (2005) Up from Slavery: Slaves at the Cape, their origins, treatments and contribution. Cape Town: Ampersand Press and the Univeristy of Western Cape.

10. JakobssonM, ScholzSW, ScheetP, GibbsJR, VanLiereJM, et al. (2008) Genotype, haplotype and copy-number variation in worldwide human populations. Nature 451: 998–1003.

11. NovembreJ, JohnsonT, BrycK, KutalikZ, BoykoAR, et al. (2008) Genes mirror geography within Europe. Nature 456: 98–101.

12. AutonA, BrycK, BoykoAR, LohmuellerKE, NovembreJ, et al. (2009) Global distribution of genomic diversity underscores rich complex history of continental human populations. Genome Res 19: 795–803.

13. LiH, DurbinR (2011) Inference of human population history from individual whole-genome sequences. Nature 475: 493–496.

14. SchlebuschCM, NaidooT, SoodyallH (2009) SNaPshot minisequencing to resolve mitochondrial macro-haplogroups found in Africa. Electrophoresis 30: 3657–3664.

15. NaidooT, SchlebuschCM, MakkanH, PatelP, MahabeerR, et al. (2010) Development of a single base extension method to resolve Y chromosome haplogroups in sub-Saharan African populations. Investig Genet 1: 6.

16. Quintana-MurciL, HarmantC, QuachH, BalanovskyO, ZaporozhchenkoV, et al. (2010) Strong maternal Khoisan contribution to the South African coloured population: a case of gender-biased admixture. Am J Hum Genet 86: 611–620.

17. PattersonN, PetersenDC, van der RossRE, SudoyoH, GlashoffRH, et al. (2010) Genetic structure of a unique admixed population: implications for medical research. Hum Mol Genet 19: 411–419.

18. de WitE, DelportW, RugamikaCE, MeintjesA, MöllerM, et al. (2010) Genome-wide analysis of the structure of the South African Coloured Population in the Western Cape. Hum Genet 128: 145–153.

19. GonderMK, MortensenHM, ReedFA, de SousaA, TishkoffSA (2007) Whole-mtDNA genome sequence analysis of ancient African lineages. Mol Biol Evol 24: 757–768.

20. TishkoffSA, GonderMK, HennBM, MortensenH, KnightA, et al. (2007) History of click-speaking populations of Africa inferred from mtDNA and Y Chromosome genetic variation. Mol Biol Evol 24: 2180–2195.

21. CrucianiF, TrombettaB, MassaiaA, Destro-BisolG, SellittoD, ScozzariR (2011) A revised root for the human Y-chromosomal phylogenetic tree: The origin of patrilineal diversity in Africa. Am J Hum Genet 88: 814–818.

22. CrucianiF, La FrattaR, SantolamazzaP, SellittoD, PasconeR, et al. (2004) Phylogeographic analysis of haplogroup E3b (E-M215) Y chromosomes reveals multiple migratory events within and out of Africa. Am J Hum Genet 74: 1014–1022.

23. de FilippoC, BarbieriC, WhittenM, MpolokaSW, GunnarsdóttirED, et al. (2011) Y-chromosomal variation in sub-Saharan Africa: insights into the history of Niger-Congo groups. Mol Biol Evol 28: 1255–1269.

24. PritchardJK, StephensM, DonnellyP (2000) Inference of population structure using multilocus genotype data. Genet 155: 945–959.

25. NievergeltCM, LibigerO, SchorkN (2007) Generalized analysis of molecular variance. PLoS Genet 3: e51 doi:10.1371/journal.pgen.0030051

26. McEvoyBP, PowellJE, GoddardME, VisscherPM (2011) Human population dispersal “Out of Africa” estimated from linkage disequilibrium and allele frequencies of SNPs. Genome Res 21: 821–829.

27. Smith BD (1995) The mergence of agriculture. Freeman, New York, pp 231.

28. ReichD, NallsMA, KaoWH, AkylbekovaEL, TandonA, et al. (2009) Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene. PLoS Genet 5: e1000360 doi:10.1371/journal.pgen.1000360

29. HancockAM, WitonskyDB, Alkorta-AranburuG, BeallCM, GebremedhinA, et al. (2011) Adaptations to Climate-Mediated Selective Pressures in Humans. PLoS Genet 7: e1001375 doi:10.1371/journal.pgen.1001375

30. KimUK, JorgensonE, CoonH, LeppertM, RischN, DraynaD (2003) Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide. Science 299: 1221–1225.

31. SabbaghA, DarluP, Crouau-RoyB, PoloniES (2011) Arylamine N-acetyltransferase 2 (NAT2) genetic diversity and traditional subsistence: a worldwide population survey. PLoS ONE 6: e18507 doi:10.1371/journal.pone.0018507

32. DolphinCT, BeckettDJ, JanmohamedA, CullingfordTE, SmithRL, et al. (1998) The flavin-containing monooxygenase 2 gene (FMO2) of humans, but not of other primates, encodes a truncated, nonfunctional protein. J Biol Chem 273: 30599–30607.

33. WhetstineJR, YuehMF, McCarverDG, WilliamsDE, ParkCS, et al. (2000) Ethnic differences in human flavin-containing monooxygenase 2 (FMO2) polymorphisms: detection of expressed protein in African-Americans. Toxicol App Pharm 168: 216–224.

34. LottaT, VidgrenJ, TilgmannC, UlmanenI, MelénK, et al. (1995) Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme. Biochem 34: 4202–4210.

35. SmolkaMN, SchumannG, WraseJ, GrüsserSM, FlorH, et al. (2005) Catechol-O-methyltransferase val158met genotype affects processing of emotional stimuli in the amygdala and prefrontal cortex. J Neuroscience 25: 836–842.

36. SteinDJ, NewmanTK, SavitzJ, RamesarR (2006) Warriors versus worriers: the role of COMT gene variants. Cent Nervous System Spect 11: 745–748.

37. HeinzA, SmolkaMN (2006) The effects of catechol O-methyltransferase genotype on brain activation elicited by affective stimuli and cognitive tasks. Rev Neuroscience 17: 359–367.

38. RoseJE, BehmFM, DrgonT, JohnsonC, UhlGR (2010) Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. Mol Med 16: 247–253.

39. WyndhamCH, StrydomNB, WardJS, MorrisonJF, WilliamsCG, et al. (1964) Physiological reactions to heat of Bushmen and of unacclimatized and acclimatized Bantu. J App Phys 19: 885–888.

40. Bradlow FR, Cairns M (1978) The early Cape Muslims: A study of their mosques, genealogy and origins. Cape Town: A.A. Balkema.

41. YoshiuraK, KinoshitaA, IshidaT, NinokataA, IshikawaT, et al. (2006) A SNP in the ABCC11 gene is the determinant of human earwax type. Nat Genet 38: 324–330.

42. YoshidaA, HuangIY, IkawaM (1984) Molecular abnormality of an inactive aldehyde dehydrogenase variant commonly found in Orientals. Proc Natl Acad Sci U S A 81: 258–261.

43. AlexanderDH, NovembreJ, LangeK (2009) Fast model-based estimation of ancestry in unrelated individuals. Genome Res 19: 1655–1664.

44. Indian Genome Variation Consortium (2008) Genetic landscape of the people of India: a canvas for disease gene exploration. J Genet 87: 3–20.

45. NarangA, JhaP, RawatV, MukhopadhyayA, MukhopadhayayA, et al. (2011) Recent admixture in an Indian population of African ancestry. Am J Hum Genet 89: 111–120.

46. GautamP, JhaP, KumarD, TyagiS, VarmaB, et al. (2012) Spectrum of large copy number variations in 26 diverse Indian populations: potential involvement in phenotypic diversity. Hum Genet 131: 131–143.

47. Swanson FS, Harries J (2001) ‘Ja! So was District Six! But it was a beautiful place’: Oral histories, memory and identity. Cape Town: David Phillip.

48. RichardsonPJ, BoydR, BettingerRL (2001) Was agriculture impossible during the Pleistocene but mandatory during the Holocene? A climate change hypothesis. Am Antiquity 66: 387–411.

49. Smith AB, Malherbe C, Guenther M, Berens P (2000) The Bushmen of southern Africa. A foraging society in transition. David Philip Publishers, Cape Town, South Africa.

50. Lee RB (2003) The Dobe Ju/'hoansi. Case studies in cultural anthropology. Thomson Learning inc., Canada, The J/'hoansi and their neighbors pp 141–150, Perceptions and directions of social change pp 152–159.

51. Marshall Thomas E (1989) The harmless people. Second Vintage Books Edition.

52. Lewis-Williams JD (1990) Discovering southern African rock art. David Philip Publishers, Cape Town, South Africa.

53. Schapera I (1930) The Khoisan Peoples of South Africa: Bushmen and Hottentots. Lowe and Brydone Printers, London pp 51–59.

54. Huffman TN (1992) Southern Africa to the south of the Zambesi, in UNESCO General History of Africa III. Africa from 7th to 11th Century: 7th century, pp 318.

55. BowcockAM, KiddJR, MountainJL, HebertJM, CarotenutoL, et al. (1991) Drift, admixture, and selection in human evolution: a study with DNA polymorphisms. Proc Natl Acad Sci U S A 88: 839–843.

56. TangH, ChoudhryS, MeiR, MorganM, Rodriguez-CintronW, et al. (2007) Recent genetic selection in the ancestral admixture of Puerto Ricans. Am J Hum Genet 81: 626–633.

57. LohmuellerKE, BustamanteCD, ClarkAG (2011) Detecting directional selection in the presence of recent admixture in African-Americans. Genetics 187: 823–835.

58. HinchAG, TandonA, PattersonN, SongY, RohlandN, et al. (2011) The landscape of recombination in African Americans. Nature 476: 170–175.

59. WegmannD, KessnerDE, VeeramahKR, MathiasRA, NicolaeDL, et al. (2011) Recombination rates in admixed individuals identified by ancestry-based inference. Nat Genet 43: 847–853.

60. KongA, ThorleifssonG, GudbjartssonDF, MassonG, SigurdssonA, et al. (2010) Fine-scale recombination rate differences between sexes, populations and individuals. Nature 467: 1099–1103.

61. Pickrell JK, Patterson N, Barbieri C, Berthold F, Gerlach L, et al.. (2012) The genetic prehistory of southern Africa. Cornell University Library.

62. Schlebusch CM, Skoglund P, Sjödin P, Gattepaille LM, Hernandez D, et al.. (2012) Genomic variation in seven Khoe-San groups reveals adaptation and complex African history. Science, In press.

63. Marshall Thomas E (2006) The old way. A story of the first people. Picador, New York. Lineage pp 16–23, The Kalahari pp43–53, Hunting pp 86–106.

64. GüldemannT (2008) A linguistic's view: Khoe-Kwadi speakers as the earliest food-producers of Southern Africa. Southern African Humanities 20: 93–132.

65. Kaschula R (1997) The Heritage Library of African People: Xhosa. New York: The Rosen Publishing Group, Inc.

66. Böeseken AJ (1977) Slaves and Free Blacks at the Cape 1658–1700. Cape Town: Tafelberg.

67. Orizio R (2001) Lost White Tribes: The End of Privilege and the Last Colonials in Sri Lanka, Jamaica, Brazil, Haiti, Namibia, and Guadeloupe. New York: Free Press.

68. van OvenM, KayserM (2009) Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation. Human Mutation 30: E386–394.

69. KarafetTM, MendezFL, MeilermanMB, UnderhillPA, ZeguraSL, HammerMF (2008) New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree. Genome Res 18: 830–838.

70. PurcellS, NealeB, Todd-BrownK, ThomasL, FerreiraMA, et al. (2007) PLINK: a toolset for whole-genome association and population-based linkage analysis. Am J Hum Genet 81: 559–575.

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2013 Číslo 3
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Aktuální možnosti diagnostiky a léčby litiáz
nový kurz
Autori: MUDr. Tomáš Ürge, PhD.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#