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Genomic architecture of phenotypic extremes in a wild cervid

Identifying the genes underlying fitness-related traits such as body size and male ornamentation can provide tools for conservation and management and are often subject to various selective pressures. Here we performed high-depth whole genome re-sequencing of pools of individuals representing the ph...

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Autores principales: Anderson, S. J., Côté, S. D., Richard, J. H., Shafer, A. B. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841092/
https://www.ncbi.nlm.nih.gov/pubmed/35151275
http://dx.doi.org/10.1186/s12864-022-08333-x
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author Anderson, S. J.
Côté, S. D.
Richard, J. H.
Shafer, A. B. A.
author_facet Anderson, S. J.
Côté, S. D.
Richard, J. H.
Shafer, A. B. A.
author_sort Anderson, S. J.
collection PubMed
description Identifying the genes underlying fitness-related traits such as body size and male ornamentation can provide tools for conservation and management and are often subject to various selective pressures. Here we performed high-depth whole genome re-sequencing of pools of individuals representing the phenotypic extremes for antler and body size in white-tailed deer (Odocoileus virginianus). Samples were selected from a tissue repository containing phenotypic data for 4,466 male white-tailed deer from Anticosti Island, Quebec, with four pools representing the extreme phenotypes for antler and body size after controlling for age. Our results revealed a largely homogenous population but detected highly divergent windows between pools for both traits, with the mean allele frequency difference of 14% for and 13% for antler and body SNPs in outlier windows, respectively. Genes in outlier antler windows were enriched for pathways associated with cell death and protein metabolism and some of the most differentiated windows included genes associated with oncogenic pathways and reproduction, processes consistent with antler evolution and growth. Genes associated with body size were more nuanced, suggestive of a highly complex trait. Overall, this study revealed the complex genomic make-up of both antler morphology and body size in free-ranging white-tailed deer and identified target loci for additional analyses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08333-x.
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spelling pubmed-88410922022-02-16 Genomic architecture of phenotypic extremes in a wild cervid Anderson, S. J. Côté, S. D. Richard, J. H. Shafer, A. B. A. BMC Genomics Research Identifying the genes underlying fitness-related traits such as body size and male ornamentation can provide tools for conservation and management and are often subject to various selective pressures. Here we performed high-depth whole genome re-sequencing of pools of individuals representing the phenotypic extremes for antler and body size in white-tailed deer (Odocoileus virginianus). Samples were selected from a tissue repository containing phenotypic data for 4,466 male white-tailed deer from Anticosti Island, Quebec, with four pools representing the extreme phenotypes for antler and body size after controlling for age. Our results revealed a largely homogenous population but detected highly divergent windows between pools for both traits, with the mean allele frequency difference of 14% for and 13% for antler and body SNPs in outlier windows, respectively. Genes in outlier antler windows were enriched for pathways associated with cell death and protein metabolism and some of the most differentiated windows included genes associated with oncogenic pathways and reproduction, processes consistent with antler evolution and growth. Genes associated with body size were more nuanced, suggestive of a highly complex trait. Overall, this study revealed the complex genomic make-up of both antler morphology and body size in free-ranging white-tailed deer and identified target loci for additional analyses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08333-x. BioMed Central 2022-02-12 /pmc/articles/PMC8841092/ /pubmed/35151275 http://dx.doi.org/10.1186/s12864-022-08333-x 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
Anderson, S. J.
Côté, S. D.
Richard, J. H.
Shafer, A. B. A.
Genomic architecture of phenotypic extremes in a wild cervid
title Genomic architecture of phenotypic extremes in a wild cervid
title_full Genomic architecture of phenotypic extremes in a wild cervid
title_fullStr Genomic architecture of phenotypic extremes in a wild cervid
title_full_unstemmed Genomic architecture of phenotypic extremes in a wild cervid
title_short Genomic architecture of phenotypic extremes in a wild cervid
title_sort genomic architecture of phenotypic extremes in a wild cervid
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841092/
https://www.ncbi.nlm.nih.gov/pubmed/35151275
http://dx.doi.org/10.1186/s12864-022-08333-x
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