Cargando…

Ancient genomes reveal complex patterns of population movement, interaction, and replacement in sub-Saharan Africa

Africa hosts the greatest human genetic diversity globally, but legacies of ancient population interactions and dispersals across the continent remain understudied. Here, we report genome-wide data from 20 ancient sub-Saharan African individuals, including the first reported ancient DNA from the DRC...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Ke, Goldstein, Steven, Bleasdale, Madeleine, Clist, Bernard, Bostoen, Koen, Bakwa-Lufu, Paul, Buck, Laura T., Crowther, Alison, Dème, Alioune, McIntosh, Roderick J., Mercader, Julio, Ogola, Christine, Power, Robert C., Sawchuk, Elizabeth, Robertshaw, Peter, Wilmsen, Edwin N., Petraglia, Michael, Ndiema, Emmanuel, Manthi, Fredrick K., Krause, Johannes, Roberts, Patrick, Boivin, Nicole, Schiffels, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292641/
https://www.ncbi.nlm.nih.gov/pubmed/32582847
http://dx.doi.org/10.1126/sciadv.aaz0183
_version_ 1783546149127323648
author Wang, Ke
Goldstein, Steven
Bleasdale, Madeleine
Clist, Bernard
Bostoen, Koen
Bakwa-Lufu, Paul
Buck, Laura T.
Crowther, Alison
Dème, Alioune
McIntosh, Roderick J.
Mercader, Julio
Ogola, Christine
Power, Robert C.
Sawchuk, Elizabeth
Robertshaw, Peter
Wilmsen, Edwin N.
Petraglia, Michael
Ndiema, Emmanuel
Manthi, Fredrick K.
Krause, Johannes
Roberts, Patrick
Boivin, Nicole
Schiffels, Stephan
author_facet Wang, Ke
Goldstein, Steven
Bleasdale, Madeleine
Clist, Bernard
Bostoen, Koen
Bakwa-Lufu, Paul
Buck, Laura T.
Crowther, Alison
Dème, Alioune
McIntosh, Roderick J.
Mercader, Julio
Ogola, Christine
Power, Robert C.
Sawchuk, Elizabeth
Robertshaw, Peter
Wilmsen, Edwin N.
Petraglia, Michael
Ndiema, Emmanuel
Manthi, Fredrick K.
Krause, Johannes
Roberts, Patrick
Boivin, Nicole
Schiffels, Stephan
author_sort Wang, Ke
collection PubMed
description Africa hosts the greatest human genetic diversity globally, but legacies of ancient population interactions and dispersals across the continent remain understudied. Here, we report genome-wide data from 20 ancient sub-Saharan African individuals, including the first reported ancient DNA from the DRC, Uganda, and Botswana. These data demonstrate the contraction of diverse, once contiguous hunter-gatherer populations, and suggest the resistance to interaction with incoming pastoralists of delayed-return foragers in aquatic environments. We refine models for the spread of food producers into eastern and southern Africa, demonstrating more complex trajectories of admixture than previously suggested. In Botswana, we show that Bantu ancestry post-dates admixture between pastoralists and foragers, suggesting an earlier spread of pastoralism than farming to southern Africa. Our findings demonstrate how processes of migration and admixture have markedly reshaped the genetic map of sub-Saharan Africa in the past few millennia and highlight the utility of combined archaeological and archaeogenetic approaches.
format Online
Article
Text
id pubmed-7292641
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Association for the Advancement of Science
record_format MEDLINE/PubMed
spelling pubmed-72926412020-06-23 Ancient genomes reveal complex patterns of population movement, interaction, and replacement in sub-Saharan Africa Wang, Ke Goldstein, Steven Bleasdale, Madeleine Clist, Bernard Bostoen, Koen Bakwa-Lufu, Paul Buck, Laura T. Crowther, Alison Dème, Alioune McIntosh, Roderick J. Mercader, Julio Ogola, Christine Power, Robert C. Sawchuk, Elizabeth Robertshaw, Peter Wilmsen, Edwin N. Petraglia, Michael Ndiema, Emmanuel Manthi, Fredrick K. Krause, Johannes Roberts, Patrick Boivin, Nicole Schiffels, Stephan Sci Adv Research Articles Africa hosts the greatest human genetic diversity globally, but legacies of ancient population interactions and dispersals across the continent remain understudied. Here, we report genome-wide data from 20 ancient sub-Saharan African individuals, including the first reported ancient DNA from the DRC, Uganda, and Botswana. These data demonstrate the contraction of diverse, once contiguous hunter-gatherer populations, and suggest the resistance to interaction with incoming pastoralists of delayed-return foragers in aquatic environments. We refine models for the spread of food producers into eastern and southern Africa, demonstrating more complex trajectories of admixture than previously suggested. In Botswana, we show that Bantu ancestry post-dates admixture between pastoralists and foragers, suggesting an earlier spread of pastoralism than farming to southern Africa. Our findings demonstrate how processes of migration and admixture have markedly reshaped the genetic map of sub-Saharan Africa in the past few millennia and highlight the utility of combined archaeological and archaeogenetic approaches. American Association for the Advancement of Science 2020-06-12 /pmc/articles/PMC7292641/ /pubmed/32582847 http://dx.doi.org/10.1126/sciadv.aaz0183 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Wang, Ke
Goldstein, Steven
Bleasdale, Madeleine
Clist, Bernard
Bostoen, Koen
Bakwa-Lufu, Paul
Buck, Laura T.
Crowther, Alison
Dème, Alioune
McIntosh, Roderick J.
Mercader, Julio
Ogola, Christine
Power, Robert C.
Sawchuk, Elizabeth
Robertshaw, Peter
Wilmsen, Edwin N.
Petraglia, Michael
Ndiema, Emmanuel
Manthi, Fredrick K.
Krause, Johannes
Roberts, Patrick
Boivin, Nicole
Schiffels, Stephan
Ancient genomes reveal complex patterns of population movement, interaction, and replacement in sub-Saharan Africa
title Ancient genomes reveal complex patterns of population movement, interaction, and replacement in sub-Saharan Africa
title_full Ancient genomes reveal complex patterns of population movement, interaction, and replacement in sub-Saharan Africa
title_fullStr Ancient genomes reveal complex patterns of population movement, interaction, and replacement in sub-Saharan Africa
title_full_unstemmed Ancient genomes reveal complex patterns of population movement, interaction, and replacement in sub-Saharan Africa
title_short Ancient genomes reveal complex patterns of population movement, interaction, and replacement in sub-Saharan Africa
title_sort ancient genomes reveal complex patterns of population movement, interaction, and replacement in sub-saharan africa
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292641/
https://www.ncbi.nlm.nih.gov/pubmed/32582847
http://dx.doi.org/10.1126/sciadv.aaz0183
work_keys_str_mv AT wangke ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT goldsteinsteven ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT bleasdalemadeleine ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT clistbernard ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT bostoenkoen ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT bakwalufupaul ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT bucklaurat ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT crowtheralison ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT demealioune ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT mcintoshroderickj ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT mercaderjulio ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT ogolachristine ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT powerrobertc ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT sawchukelizabeth ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT robertshawpeter ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT wilmsenedwinn ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT petragliamichael ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT ndiemaemmanuel ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT manthifredrickk ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT krausejohannes ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT robertspatrick ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT boivinnicole ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica
AT schiffelsstephan ancientgenomesrevealcomplexpatternsofpopulationmovementinteractionandreplacementinsubsaharanafrica