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Identifying loci under selection via explicit demographic models
Adaptive genetic variation is a function of both selective and neutral forces. To accurately identify adaptive loci, it is thus critical to account for demographic history. Theory suggests that signatures of selection can be inferred using the coalescent, following the premise that genealogies of se...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596768/ https://www.ncbi.nlm.nih.gov/pubmed/33964107 http://dx.doi.org/10.1111/1755-0998.13415 |
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author | Luqman, Hirzi Widmer, Alex Fior, Simone Wegmann, Daniel |
author_facet | Luqman, Hirzi Widmer, Alex Fior, Simone Wegmann, Daniel |
author_sort | Luqman, Hirzi |
collection | PubMed |
description | Adaptive genetic variation is a function of both selective and neutral forces. To accurately identify adaptive loci, it is thus critical to account for demographic history. Theory suggests that signatures of selection can be inferred using the coalescent, following the premise that genealogies of selected loci deviate from neutral expectations. Here, we build on this theory to develop an analytical framework to identify loci under selection via explicit demographic models (LSD). Under this framework, signatures of selection are inferred through deviations in demographic parameters, rather than through summary statistics directly, and demographic history is accounted for explicitly. Leveraging the property of demographic models to incorporate directionality, we show that LSD can provide information on the environment in which selection acts on a population. This can prove useful in elucidating the selective processes underlying local adaptation, by characterizing genetic trade‐offs and extending the concepts of antagonistic pleiotropy and conditional neutrality from ecological theory to practical application in genomic data. We implement LSD via approximate Bayesian computation and demonstrate, via simulations, that LSD (a) has high power to identify selected loci across a large range of demographic‐selection regimes, (b) outperforms commonly applied genome‐scan methods under complex demographies and (c) accurately infers the directionality of selection for identified candidates. Using the same simulations, we further characterize the behaviour of isolation‐with‐migration models conducive to the study of local adaptation under regimes of selection. Finally, we demonstrate an application of LSD by detecting loci and characterizing genetic trade‐offs underlying flower colour in Antirrhinum majus. |
format | Online Article Text |
id | pubmed-8596768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85967682021-11-22 Identifying loci under selection via explicit demographic models Luqman, Hirzi Widmer, Alex Fior, Simone Wegmann, Daniel Mol Ecol Resour RESOURCE ARTICLES Adaptive genetic variation is a function of both selective and neutral forces. To accurately identify adaptive loci, it is thus critical to account for demographic history. Theory suggests that signatures of selection can be inferred using the coalescent, following the premise that genealogies of selected loci deviate from neutral expectations. Here, we build on this theory to develop an analytical framework to identify loci under selection via explicit demographic models (LSD). Under this framework, signatures of selection are inferred through deviations in demographic parameters, rather than through summary statistics directly, and demographic history is accounted for explicitly. Leveraging the property of demographic models to incorporate directionality, we show that LSD can provide information on the environment in which selection acts on a population. This can prove useful in elucidating the selective processes underlying local adaptation, by characterizing genetic trade‐offs and extending the concepts of antagonistic pleiotropy and conditional neutrality from ecological theory to practical application in genomic data. We implement LSD via approximate Bayesian computation and demonstrate, via simulations, that LSD (a) has high power to identify selected loci across a large range of demographic‐selection regimes, (b) outperforms commonly applied genome‐scan methods under complex demographies and (c) accurately infers the directionality of selection for identified candidates. Using the same simulations, we further characterize the behaviour of isolation‐with‐migration models conducive to the study of local adaptation under regimes of selection. Finally, we demonstrate an application of LSD by detecting loci and characterizing genetic trade‐offs underlying flower colour in Antirrhinum majus. John Wiley and Sons Inc. 2021-06-03 2021-11 /pmc/articles/PMC8596768/ /pubmed/33964107 http://dx.doi.org/10.1111/1755-0998.13415 Text en © 2021 The Authors. Molecular Ecology Resources published by John Wiley & Sons Ltd https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RESOURCE ARTICLES Luqman, Hirzi Widmer, Alex Fior, Simone Wegmann, Daniel Identifying loci under selection via explicit demographic models |
title | Identifying loci under selection via explicit demographic models |
title_full | Identifying loci under selection via explicit demographic models |
title_fullStr | Identifying loci under selection via explicit demographic models |
title_full_unstemmed | Identifying loci under selection via explicit demographic models |
title_short | Identifying loci under selection via explicit demographic models |
title_sort | identifying loci under selection via explicit demographic models |
topic | RESOURCE ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596768/ https://www.ncbi.nlm.nih.gov/pubmed/33964107 http://dx.doi.org/10.1111/1755-0998.13415 |
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