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Human subsistence and signatures of selection on chemosensory genes
Chemosensation (olfaction, taste) is essential for detecting and assessing foods, such that dietary shifts elicit evolutionary changes in vertebrate chemosensory genes. The transition from hunting and gathering to agriculture dramatically altered how humans acquire food. Recent genetic and linguisti...
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/PMC10317983/ https://www.ncbi.nlm.nih.gov/pubmed/37400713 http://dx.doi.org/10.1038/s42003-023-05047-y |
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author | Veilleux, Carrie C. Garrett, Eva C. Pajic, Petar Saitou, Marie Ochieng, Joseph Dagsaan, Lilia D. Dominy, Nathaniel J. Perry, George H. Gokcumen, Omer Melin, Amanda D. |
author_facet | Veilleux, Carrie C. Garrett, Eva C. Pajic, Petar Saitou, Marie Ochieng, Joseph Dagsaan, Lilia D. Dominy, Nathaniel J. Perry, George H. Gokcumen, Omer Melin, Amanda D. |
author_sort | Veilleux, Carrie C. |
collection | PubMed |
description | Chemosensation (olfaction, taste) is essential for detecting and assessing foods, such that dietary shifts elicit evolutionary changes in vertebrate chemosensory genes. The transition from hunting and gathering to agriculture dramatically altered how humans acquire food. Recent genetic and linguistic studies suggest agriculture may have precipitated olfactory degeneration. Here, we explore the effects of subsistence behaviors on olfactory (OR) and taste (TASR) receptor genes among rainforest foragers and neighboring agriculturalists in Africa and Southeast Asia. We analyze 378 functional OR and 26 functional TASR genes in 133 individuals across populations in Uganda (Twa, Sua, BaKiga) and the Philippines (Agta, Mamanwa, Manobo) with differing subsistence histories. We find no evidence of relaxed selection on chemosensory genes in agricultural populations. However, we identify subsistence-related signatures of local adaptation on chemosensory genes within each geographic region. Our results highlight the importance of culture, subsistence economy, and drift in human chemosensory perception. |
format | Online Article Text |
id | pubmed-10317983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103179832023-07-05 Human subsistence and signatures of selection on chemosensory genes Veilleux, Carrie C. Garrett, Eva C. Pajic, Petar Saitou, Marie Ochieng, Joseph Dagsaan, Lilia D. Dominy, Nathaniel J. Perry, George H. Gokcumen, Omer Melin, Amanda D. Commun Biol Article Chemosensation (olfaction, taste) is essential for detecting and assessing foods, such that dietary shifts elicit evolutionary changes in vertebrate chemosensory genes. The transition from hunting and gathering to agriculture dramatically altered how humans acquire food. Recent genetic and linguistic studies suggest agriculture may have precipitated olfactory degeneration. Here, we explore the effects of subsistence behaviors on olfactory (OR) and taste (TASR) receptor genes among rainforest foragers and neighboring agriculturalists in Africa and Southeast Asia. We analyze 378 functional OR and 26 functional TASR genes in 133 individuals across populations in Uganda (Twa, Sua, BaKiga) and the Philippines (Agta, Mamanwa, Manobo) with differing subsistence histories. We find no evidence of relaxed selection on chemosensory genes in agricultural populations. However, we identify subsistence-related signatures of local adaptation on chemosensory genes within each geographic region. Our results highlight the importance of culture, subsistence economy, and drift in human chemosensory perception. Nature Publishing Group UK 2023-07-03 /pmc/articles/PMC10317983/ /pubmed/37400713 http://dx.doi.org/10.1038/s42003-023-05047-y 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 Veilleux, Carrie C. Garrett, Eva C. Pajic, Petar Saitou, Marie Ochieng, Joseph Dagsaan, Lilia D. Dominy, Nathaniel J. Perry, George H. Gokcumen, Omer Melin, Amanda D. Human subsistence and signatures of selection on chemosensory genes |
title | Human subsistence and signatures of selection on chemosensory genes |
title_full | Human subsistence and signatures of selection on chemosensory genes |
title_fullStr | Human subsistence and signatures of selection on chemosensory genes |
title_full_unstemmed | Human subsistence and signatures of selection on chemosensory genes |
title_short | Human subsistence and signatures of selection on chemosensory genes |
title_sort | human subsistence and signatures of selection on chemosensory genes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317983/ https://www.ncbi.nlm.nih.gov/pubmed/37400713 http://dx.doi.org/10.1038/s42003-023-05047-y |
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