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Selection and demography drive range-wide patterns of MHC-DRB variation in mule deer
BACKGROUND: Standing genetic variation is important especially in immune response-related genes because of threats to wild populations like the emergence of novel pathogens. Genetic variation at the major histocompatibility complex (MHC), which is crucial in activating the adaptive immune response,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988406/ https://www.ncbi.nlm.nih.gov/pubmed/35387584 http://dx.doi.org/10.1186/s12862-022-01998-8 |
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author | Cook, Rachel M. Suttner, Brittany Giglio, Rachael M. Haines, Margaret L. Latch, Emily K. |
author_facet | Cook, Rachel M. Suttner, Brittany Giglio, Rachael M. Haines, Margaret L. Latch, Emily K. |
author_sort | Cook, Rachel M. |
collection | PubMed |
description | BACKGROUND: Standing genetic variation is important especially in immune response-related genes because of threats to wild populations like the emergence of novel pathogens. Genetic variation at the major histocompatibility complex (MHC), which is crucial in activating the adaptive immune response, is influenced by both natural selection and historical population demography, and their relative roles can be difficult to disentangle. To provide insight into the influences of natural selection and demography on MHC evolution in large populations, we analyzed geographic patterns of variation at the MHC class II DRB exon 2 locus in mule deer (Odocoileus hemionus) using sequence data collected across their entire broad range. RESULTS: We identified 31 new MHC-DRB alleles which were phylogenetically similar to other cervid MHC alleles, and one allele that was shared with white-tailed deer (Odocoileus virginianus). We found evidence for selection on the MHC including high dN/dS ratios, positive neutrality tests, deviations from Hardy–Weinberg Equilibrium (HWE) and a stronger pattern of isolation-by-distance (IBD) than expected under neutrality. Historical demography also shaped variation at the MHC, as indicated by similar spatial patterns of variation between MHC and microsatellite loci and a lack of association between genetic variation at either locus type and environmental variables. CONCLUSIONS: Our results show that both natural selection and historical demography are important drivers in the evolution of the MHC in mule deer and work together to shape functional variation and the evolution of the adaptive immune response in large, well-connected populations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12862-022-01998-8. |
format | Online Article Text |
id | pubmed-8988406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89884062022-04-08 Selection and demography drive range-wide patterns of MHC-DRB variation in mule deer Cook, Rachel M. Suttner, Brittany Giglio, Rachael M. Haines, Margaret L. Latch, Emily K. BMC Ecol Evol Research BACKGROUND: Standing genetic variation is important especially in immune response-related genes because of threats to wild populations like the emergence of novel pathogens. Genetic variation at the major histocompatibility complex (MHC), which is crucial in activating the adaptive immune response, is influenced by both natural selection and historical population demography, and their relative roles can be difficult to disentangle. To provide insight into the influences of natural selection and demography on MHC evolution in large populations, we analyzed geographic patterns of variation at the MHC class II DRB exon 2 locus in mule deer (Odocoileus hemionus) using sequence data collected across their entire broad range. RESULTS: We identified 31 new MHC-DRB alleles which were phylogenetically similar to other cervid MHC alleles, and one allele that was shared with white-tailed deer (Odocoileus virginianus). We found evidence for selection on the MHC including high dN/dS ratios, positive neutrality tests, deviations from Hardy–Weinberg Equilibrium (HWE) and a stronger pattern of isolation-by-distance (IBD) than expected under neutrality. Historical demography also shaped variation at the MHC, as indicated by similar spatial patterns of variation between MHC and microsatellite loci and a lack of association between genetic variation at either locus type and environmental variables. CONCLUSIONS: Our results show that both natural selection and historical demography are important drivers in the evolution of the MHC in mule deer and work together to shape functional variation and the evolution of the adaptive immune response in large, well-connected populations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12862-022-01998-8. BioMed Central 2022-04-06 /pmc/articles/PMC8988406/ /pubmed/35387584 http://dx.doi.org/10.1186/s12862-022-01998-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Cook, Rachel M. Suttner, Brittany Giglio, Rachael M. Haines, Margaret L. Latch, Emily K. Selection and demography drive range-wide patterns of MHC-DRB variation in mule deer |
title | Selection and demography drive range-wide patterns of MHC-DRB variation in mule deer |
title_full | Selection and demography drive range-wide patterns of MHC-DRB variation in mule deer |
title_fullStr | Selection and demography drive range-wide patterns of MHC-DRB variation in mule deer |
title_full_unstemmed | Selection and demography drive range-wide patterns of MHC-DRB variation in mule deer |
title_short | Selection and demography drive range-wide patterns of MHC-DRB variation in mule deer |
title_sort | selection and demography drive range-wide patterns of mhc-drb variation in mule deer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988406/ https://www.ncbi.nlm.nih.gov/pubmed/35387584 http://dx.doi.org/10.1186/s12862-022-01998-8 |
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