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Article: Both selection and drift drive the spatial pattern of adaptive genetic variation in a wild mammal

TitleBoth selection and drift drive the spatial pattern of adaptive genetic variation in a wild mammal
Authors
Keywordsbalancing selection on supertype
European badgers
genetic diversity
genetic drift
major histocompatibility complex
pathogen-mediated selection
Issue Date1-Jan-2023
PublisherOxford University Press
Citation
Evolution: International Journal of Organic Evolution, 2023, v. 77, n. 1, p. 221-238 How to Cite?
Abstract

The major histocompatibility complex (MHC) has been intensively studied for the relative effects of different evolutionary forces in recent decades. Pathogen-mediated balancing selection is generally thought to explain the high polymorphism observed in MHC genes, but it is still unclear to what extent MHC diversity is shaped by selection relative to neutral drift. In this study, we genotyped MHC class II DRB genes and 15 neutral microsatellite loci across 26 geographic populations of European badgers (Meles meles) covering most of their geographic range. By comparing variation of microsatellite and diversity of MHC at different levels, we demonstrate that both balancing selection and drift have shaped the evolution of MHC genes. When only MHC allelic identity was investigated, the spatial pattern of MHC variation was similar to that of microsatellites. By contrast, when functional aspects of the MHC diversity (e.g., immunological supertypes) were considered, balancing selection appears to decrease genetic structuring across populations. Our comprehensive sampling and analytical approach enable us to conclude that the likely mechanisms of selection are heterozygote advantage and/or rare-allele advantage. This study is a clear demonstration of how both balancing selection and genetic drift simultaneously affect the evolution of MHC genes in a widely distributed wild mammal. © 2022 The Author(s). Published by Oxford University Press on behalf of The Society for the Study of Evolution (SSE).


Persistent Identifierhttp://hdl.handle.net/10722/338772
ISSN
2023 Impact Factor: 3.1
2023 SCImago Journal Rankings: 1.235
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLam, Derek Kong-
dc.contributor.authorFrantz, Alain C-
dc.contributor.authorBurke, Terry-
dc.contributor.authorGeffen, Eli-
dc.contributor.authorSin, Simon Yung Wa-
dc.date.accessioned2024-03-11T10:31:24Z-
dc.date.available2024-03-11T10:31:24Z-
dc.date.issued2023-01-01-
dc.identifier.citationEvolution: International Journal of Organic Evolution, 2023, v. 77, n. 1, p. 221-238-
dc.identifier.issn0014-3820-
dc.identifier.urihttp://hdl.handle.net/10722/338772-
dc.description.abstract<p> <span>The major histocompatibility complex (MHC) has been intensively studied for the relative effects of different evolutionary forces in recent decades. Pathogen-mediated balancing selection is generally thought to explain the high polymorphism observed in MHC genes, but it is still unclear to what extent MHC diversity is shaped by selection relative to neutral drift. In this study, we genotyped MHC class II DRB genes and 15 neutral microsatellite loci across 26 geographic populations of European badgers (Meles meles) covering most of their geographic range. By comparing variation of microsatellite and diversity of MHC at different levels, we demonstrate that both balancing selection and drift have shaped the evolution of MHC genes. When only MHC allelic identity was investigated, the spatial pattern of MHC variation was similar to that of microsatellites. By contrast, when functional aspects of the MHC diversity (e.g., immunological supertypes) were considered, balancing selection appears to decrease genetic structuring across populations. Our comprehensive sampling and analytical approach enable us to conclude that the likely mechanisms of selection are heterozygote advantage and/or rare-allele advantage. This study is a clear demonstration of how both balancing selection and genetic drift simultaneously affect the evolution of MHC genes in a widely distributed wild mammal. © 2022 The Author(s). Published by Oxford University Press on behalf of The Society for the Study of Evolution (SSE).</span> <br></p>-
dc.languageeng-
dc.publisherOxford University Press-
dc.relation.ispartofEvolution: International Journal of Organic Evolution-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectbalancing selection on supertype-
dc.subjectEuropean badgers-
dc.subjectgenetic diversity-
dc.subjectgenetic drift-
dc.subjectmajor histocompatibility complex-
dc.subjectpathogen-mediated selection-
dc.titleBoth selection and drift drive the spatial pattern of adaptive genetic variation in a wild mammal-
dc.typeArticle-
dc.identifier.doi10.1093/evolut/qpac014-
dc.identifier.scopuseid_2-s2.0-85147046728-
dc.identifier.volume77-
dc.identifier.issue1-
dc.identifier.spage221-
dc.identifier.epage238-
dc.identifier.eissn1558-5646-
dc.identifier.isiWOS:001021686300017-
dc.identifier.issnl0014-3820-

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