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Extensive Admixture and Selective Pressure Across the Sahel Belt

Genome-wide studies of African populations have the potential to reveal powerful insights into the evolution of our species, as these diverse populations have been exposed to intense selective pressures imposed by infectious diseases, diet, and environmental factors. Within Africa, the Sahel Belt ex...

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Autores principales: Triska, Petr, Soares, Pedro, Patin, Etienne, Fernandes, Veronica, Cerny, Viktor, Pereira, Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4700964/
https://www.ncbi.nlm.nih.gov/pubmed/26614524
http://dx.doi.org/10.1093/gbe/evv236
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author Triska, Petr
Soares, Pedro
Patin, Etienne
Fernandes, Veronica
Cerny, Viktor
Pereira, Luisa
author_facet Triska, Petr
Soares, Pedro
Patin, Etienne
Fernandes, Veronica
Cerny, Viktor
Pereira, Luisa
author_sort Triska, Petr
collection PubMed
description Genome-wide studies of African populations have the potential to reveal powerful insights into the evolution of our species, as these diverse populations have been exposed to intense selective pressures imposed by infectious diseases, diet, and environmental factors. Within Africa, the Sahel Belt extensively overlaps the geographical center of several endemic infections such as malaria, trypanosomiasis, meningitis, and hemorrhagic fevers. We screened 2.5 million single nucleotide polymorphisms in 161 individuals from 13 Sahelian populations, which together with published data cover Western, Central, and Eastern Sahel, and include both nomadic and sedentary groups. We confirmed the role of this Belt as a main corridor for human migrations across the continent. Strong admixture was observed in both Central and Eastern Sahelian populations, with North Africans and Near Eastern/Arabians, respectively, but it was inexistent in Western Sahelian populations. Genome-wide local ancestry inference in admixed Sahelian populations revealed several candidate regions that were significantly enriched for non-autochthonous haplotypes, and many showed to be under positive selection. The DARC gene region in Arabs and Nubians was enriched for African ancestry, whereas the RAB3GAP1/LCT/MCM6 region in Oromo, the TAS2R gene family in Fulani, and the ALMS1/NAT8 in Turkana and Samburu were enriched for non-African ancestry. Signals of positive selection varied in terms of geographic amplitude. Some genomic regions were selected across the Belt, the most striking example being the malaria-related DARC gene. Others were Western-specific (oxytocin, calcium, and heart pathways), Eastern-specific (lipid pathways), or even population-restricted (TAS2R genes in Fulani, which may reflect sexual selection).
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spelling pubmed-47009642016-01-06 Extensive Admixture and Selective Pressure Across the Sahel Belt Triska, Petr Soares, Pedro Patin, Etienne Fernandes, Veronica Cerny, Viktor Pereira, Luisa Genome Biol Evol Research Article Genome-wide studies of African populations have the potential to reveal powerful insights into the evolution of our species, as these diverse populations have been exposed to intense selective pressures imposed by infectious diseases, diet, and environmental factors. Within Africa, the Sahel Belt extensively overlaps the geographical center of several endemic infections such as malaria, trypanosomiasis, meningitis, and hemorrhagic fevers. We screened 2.5 million single nucleotide polymorphisms in 161 individuals from 13 Sahelian populations, which together with published data cover Western, Central, and Eastern Sahel, and include both nomadic and sedentary groups. We confirmed the role of this Belt as a main corridor for human migrations across the continent. Strong admixture was observed in both Central and Eastern Sahelian populations, with North Africans and Near Eastern/Arabians, respectively, but it was inexistent in Western Sahelian populations. Genome-wide local ancestry inference in admixed Sahelian populations revealed several candidate regions that were significantly enriched for non-autochthonous haplotypes, and many showed to be under positive selection. The DARC gene region in Arabs and Nubians was enriched for African ancestry, whereas the RAB3GAP1/LCT/MCM6 region in Oromo, the TAS2R gene family in Fulani, and the ALMS1/NAT8 in Turkana and Samburu were enriched for non-African ancestry. Signals of positive selection varied in terms of geographic amplitude. Some genomic regions were selected across the Belt, the most striking example being the malaria-related DARC gene. Others were Western-specific (oxytocin, calcium, and heart pathways), Eastern-specific (lipid pathways), or even population-restricted (TAS2R genes in Fulani, which may reflect sexual selection). Oxford University Press 2015-11-26 /pmc/articles/PMC4700964/ /pubmed/26614524 http://dx.doi.org/10.1093/gbe/evv236 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Triska, Petr
Soares, Pedro
Patin, Etienne
Fernandes, Veronica
Cerny, Viktor
Pereira, Luisa
Extensive Admixture and Selective Pressure Across the Sahel Belt
title Extensive Admixture and Selective Pressure Across the Sahel Belt
title_full Extensive Admixture and Selective Pressure Across the Sahel Belt
title_fullStr Extensive Admixture and Selective Pressure Across the Sahel Belt
title_full_unstemmed Extensive Admixture and Selective Pressure Across the Sahel Belt
title_short Extensive Admixture and Selective Pressure Across the Sahel Belt
title_sort extensive admixture and selective pressure across the sahel belt
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4700964/
https://www.ncbi.nlm.nih.gov/pubmed/26614524
http://dx.doi.org/10.1093/gbe/evv236
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