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Understanding signatures of positive natural selection in human zinc transporter genes

Zinc is an essential micronutrient with a tightly regulated systemic and cellular homeostasis. In humans, some zinc transporter genes (ZTGs) have been previously reported as candidates for strong geographically restricted selective sweeps. However, since zinc homeostasis is maintained by the joint a...

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Autores principales: Roca-Umbert, Ana, Caro-Consuegra, Rocio, Londono-Correa, Diego, Rodriguez-Lozano, Gabriel Felipe, Vicente, Ruben, Bosch, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918337/
https://www.ncbi.nlm.nih.gov/pubmed/35279701
http://dx.doi.org/10.1038/s41598-022-08439-y
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author Roca-Umbert, Ana
Caro-Consuegra, Rocio
Londono-Correa, Diego
Rodriguez-Lozano, Gabriel Felipe
Vicente, Ruben
Bosch, Elena
author_facet Roca-Umbert, Ana
Caro-Consuegra, Rocio
Londono-Correa, Diego
Rodriguez-Lozano, Gabriel Felipe
Vicente, Ruben
Bosch, Elena
author_sort Roca-Umbert, Ana
collection PubMed
description Zinc is an essential micronutrient with a tightly regulated systemic and cellular homeostasis. In humans, some zinc transporter genes (ZTGs) have been previously reported as candidates for strong geographically restricted selective sweeps. However, since zinc homeostasis is maintained by the joint action of 24 ZTGs, other more subtle modes of selection could have also facilitated human adaptation to zinc availability. Here, we studied whether the complete set of ZTGs are enriched for signals of positive selection in worldwide populations and population groups from South Asia. ZTGs showed higher levels of genetic differentiation between African and non-African populations than would be randomly expected, as well as other signals of polygenic selection outside Africa. Moreover, in several South Asian population groups, ZTGs were significantly enriched for SNPs with unusually extended haplotypes and displayed SNP genotype-environmental correlations when considering zinc deficiency levels in soil in that geographical area. Our study replicated some well-characterized targets for positive selection in East Asia and sub-Saharan Africa, and proposes new candidates for follow-up in South Asia (SLC39A5) and Africa (SLC39A7). Finally, we identified candidate variants for adaptation in ZTGs that could contribute to different disease susceptibilities and zinc-related human health traits.
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spelling pubmed-89183372022-03-16 Understanding signatures of positive natural selection in human zinc transporter genes Roca-Umbert, Ana Caro-Consuegra, Rocio Londono-Correa, Diego Rodriguez-Lozano, Gabriel Felipe Vicente, Ruben Bosch, Elena Sci Rep Article Zinc is an essential micronutrient with a tightly regulated systemic and cellular homeostasis. In humans, some zinc transporter genes (ZTGs) have been previously reported as candidates for strong geographically restricted selective sweeps. However, since zinc homeostasis is maintained by the joint action of 24 ZTGs, other more subtle modes of selection could have also facilitated human adaptation to zinc availability. Here, we studied whether the complete set of ZTGs are enriched for signals of positive selection in worldwide populations and population groups from South Asia. ZTGs showed higher levels of genetic differentiation between African and non-African populations than would be randomly expected, as well as other signals of polygenic selection outside Africa. Moreover, in several South Asian population groups, ZTGs were significantly enriched for SNPs with unusually extended haplotypes and displayed SNP genotype-environmental correlations when considering zinc deficiency levels in soil in that geographical area. Our study replicated some well-characterized targets for positive selection in East Asia and sub-Saharan Africa, and proposes new candidates for follow-up in South Asia (SLC39A5) and Africa (SLC39A7). Finally, we identified candidate variants for adaptation in ZTGs that could contribute to different disease susceptibilities and zinc-related human health traits. Nature Publishing Group UK 2022-03-12 /pmc/articles/PMC8918337/ /pubmed/35279701 http://dx.doi.org/10.1038/s41598-022-08439-y Text en © The Author(s) 2022, corrected publication 2022 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
Roca-Umbert, Ana
Caro-Consuegra, Rocio
Londono-Correa, Diego
Rodriguez-Lozano, Gabriel Felipe
Vicente, Ruben
Bosch, Elena
Understanding signatures of positive natural selection in human zinc transporter genes
title Understanding signatures of positive natural selection in human zinc transporter genes
title_full Understanding signatures of positive natural selection in human zinc transporter genes
title_fullStr Understanding signatures of positive natural selection in human zinc transporter genes
title_full_unstemmed Understanding signatures of positive natural selection in human zinc transporter genes
title_short Understanding signatures of positive natural selection in human zinc transporter genes
title_sort understanding signatures of positive natural selection in human zinc transporter genes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918337/
https://www.ncbi.nlm.nih.gov/pubmed/35279701
http://dx.doi.org/10.1038/s41598-022-08439-y
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