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Identifying signatures of positive selection in human populations from North Africa
Because of its location, North Africa (NA) has witnessed continuous demographic movements with an impact on the genomes of present-day human populations. Genomic data describe a complex scenario with varying proportions of at least four main ancestry components: Maghrebi, Middle Eastern-, European-,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199912/ https://www.ncbi.nlm.nih.gov/pubmed/37210386 http://dx.doi.org/10.1038/s41598-023-35312-3 |
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author | Caro-Consuegra, Rocio Lucas-Sánchez, Marcel Comas, David Bosch, Elena |
author_facet | Caro-Consuegra, Rocio Lucas-Sánchez, Marcel Comas, David Bosch, Elena |
author_sort | Caro-Consuegra, Rocio |
collection | PubMed |
description | Because of its location, North Africa (NA) has witnessed continuous demographic movements with an impact on the genomes of present-day human populations. Genomic data describe a complex scenario with varying proportions of at least four main ancestry components: Maghrebi, Middle Eastern-, European-, and West-and-East-African-like. However, the footprint of positive selection in NA has not been studied. Here, we compile genome-wide genotyping data from 190 North Africans and individuals from surrounding populations, investigate for signatures of positive selection using allele frequencies and linkage disequilibrium-based methods and infer ancestry proportions to discern adaptive admixture from post-admixture selection events. Our results show private candidate genes for selection in NA involved in insulin processing (KIF5A), immune function (KIF5A, IL1RN, TLR3), and haemoglobin phenotypes (BCL11A). We also detect signatures of positive selection related to skin pigmentation (SLC24A5, KITLG), and immunity function (IL1R1, CD44, JAK1) shared with European populations and candidate genes associated with haemoglobin phenotypes (HPSE2, HBE1, HBG2), other immune-related (DOCK2) traits, and insulin processing (GLIS3) traits shared with West and East African populations. Finally, the SLC8A1 gene, which codifies for a sodium-calcium exchanger, was the only candidate identified under post-admixture selection in Western NA. |
format | Online Article Text |
id | pubmed-10199912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101999122023-05-22 Identifying signatures of positive selection in human populations from North Africa Caro-Consuegra, Rocio Lucas-Sánchez, Marcel Comas, David Bosch, Elena Sci Rep Article Because of its location, North Africa (NA) has witnessed continuous demographic movements with an impact on the genomes of present-day human populations. Genomic data describe a complex scenario with varying proportions of at least four main ancestry components: Maghrebi, Middle Eastern-, European-, and West-and-East-African-like. However, the footprint of positive selection in NA has not been studied. Here, we compile genome-wide genotyping data from 190 North Africans and individuals from surrounding populations, investigate for signatures of positive selection using allele frequencies and linkage disequilibrium-based methods and infer ancestry proportions to discern adaptive admixture from post-admixture selection events. Our results show private candidate genes for selection in NA involved in insulin processing (KIF5A), immune function (KIF5A, IL1RN, TLR3), and haemoglobin phenotypes (BCL11A). We also detect signatures of positive selection related to skin pigmentation (SLC24A5, KITLG), and immunity function (IL1R1, CD44, JAK1) shared with European populations and candidate genes associated with haemoglobin phenotypes (HPSE2, HBE1, HBG2), other immune-related (DOCK2) traits, and insulin processing (GLIS3) traits shared with West and East African populations. Finally, the SLC8A1 gene, which codifies for a sodium-calcium exchanger, was the only candidate identified under post-admixture selection in Western NA. Nature Publishing Group UK 2023-05-20 /pmc/articles/PMC10199912/ /pubmed/37210386 http://dx.doi.org/10.1038/s41598-023-35312-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Caro-Consuegra, Rocio Lucas-Sánchez, Marcel Comas, David Bosch, Elena Identifying signatures of positive selection in human populations from North Africa |
title | Identifying signatures of positive selection in human populations from North Africa |
title_full | Identifying signatures of positive selection in human populations from North Africa |
title_fullStr | Identifying signatures of positive selection in human populations from North Africa |
title_full_unstemmed | Identifying signatures of positive selection in human populations from North Africa |
title_short | Identifying signatures of positive selection in human populations from North Africa |
title_sort | identifying signatures of positive selection in human populations from north africa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199912/ https://www.ncbi.nlm.nih.gov/pubmed/37210386 http://dx.doi.org/10.1038/s41598-023-35312-3 |
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