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Parallel adaptation in autopolyploid Arabidopsis arenosa is dominated by repeated recruitment of shared alleles
Relative contributions of pre-existing vs de novo genomic variation to adaptation are poorly understood, especially in polyploid organisms. We assess this in high resolution using autotetraploid Arabidopsis arenosa, which repeatedly adapted to toxic serpentine soils that exhibit skewed elemental pro...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370997/ https://www.ncbi.nlm.nih.gov/pubmed/34404804 http://dx.doi.org/10.1038/s41467-021-25256-5 |
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author | Konečná, Veronika Bray, Sian Vlček, Jakub Bohutínská, Magdalena Požárová, Doubravka Choudhury, Rimjhim Roy Bollmann-Giolai, Anita Flis, Paulina Salt, David E. Parisod, Christian Yant, Levi Kolář, Filip |
author_facet | Konečná, Veronika Bray, Sian Vlček, Jakub Bohutínská, Magdalena Požárová, Doubravka Choudhury, Rimjhim Roy Bollmann-Giolai, Anita Flis, Paulina Salt, David E. Parisod, Christian Yant, Levi Kolář, Filip |
author_sort | Konečná, Veronika |
collection | PubMed |
description | Relative contributions of pre-existing vs de novo genomic variation to adaptation are poorly understood, especially in polyploid organisms. We assess this in high resolution using autotetraploid Arabidopsis arenosa, which repeatedly adapted to toxic serpentine soils that exhibit skewed elemental profiles. Leveraging a fivefold replicated serpentine invasion, we assess selection on SNPs and structural variants (TEs) in 78 resequenced individuals and discover significant parallelism in candidate genes involved in ion homeostasis. We further model parallel selection and infer repeated sweeps on a shared pool of variants in nearly all these loci, supporting theoretical expectations. A single striking exception is represented by TWO PORE CHANNEL 1, which exhibits convergent evolution from independent de novo mutations at an identical, otherwise conserved site at the calcium channel selectivity gate. Taken together, this suggests that polyploid populations can rapidly adapt to environmental extremes, calling on both pre-existing variation and novel polymorphisms. |
format | Online Article Text |
id | pubmed-8370997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83709972021-09-02 Parallel adaptation in autopolyploid Arabidopsis arenosa is dominated by repeated recruitment of shared alleles Konečná, Veronika Bray, Sian Vlček, Jakub Bohutínská, Magdalena Požárová, Doubravka Choudhury, Rimjhim Roy Bollmann-Giolai, Anita Flis, Paulina Salt, David E. Parisod, Christian Yant, Levi Kolář, Filip Nat Commun Article Relative contributions of pre-existing vs de novo genomic variation to adaptation are poorly understood, especially in polyploid organisms. We assess this in high resolution using autotetraploid Arabidopsis arenosa, which repeatedly adapted to toxic serpentine soils that exhibit skewed elemental profiles. Leveraging a fivefold replicated serpentine invasion, we assess selection on SNPs and structural variants (TEs) in 78 resequenced individuals and discover significant parallelism in candidate genes involved in ion homeostasis. We further model parallel selection and infer repeated sweeps on a shared pool of variants in nearly all these loci, supporting theoretical expectations. A single striking exception is represented by TWO PORE CHANNEL 1, which exhibits convergent evolution from independent de novo mutations at an identical, otherwise conserved site at the calcium channel selectivity gate. Taken together, this suggests that polyploid populations can rapidly adapt to environmental extremes, calling on both pre-existing variation and novel polymorphisms. Nature Publishing Group UK 2021-08-17 /pmc/articles/PMC8370997/ /pubmed/34404804 http://dx.doi.org/10.1038/s41467-021-25256-5 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Konečná, Veronika Bray, Sian Vlček, Jakub Bohutínská, Magdalena Požárová, Doubravka Choudhury, Rimjhim Roy Bollmann-Giolai, Anita Flis, Paulina Salt, David E. Parisod, Christian Yant, Levi Kolář, Filip Parallel adaptation in autopolyploid Arabidopsis arenosa is dominated by repeated recruitment of shared alleles |
title | Parallel adaptation in autopolyploid Arabidopsis arenosa is dominated by repeated recruitment of shared alleles |
title_full | Parallel adaptation in autopolyploid Arabidopsis arenosa is dominated by repeated recruitment of shared alleles |
title_fullStr | Parallel adaptation in autopolyploid Arabidopsis arenosa is dominated by repeated recruitment of shared alleles |
title_full_unstemmed | Parallel adaptation in autopolyploid Arabidopsis arenosa is dominated by repeated recruitment of shared alleles |
title_short | Parallel adaptation in autopolyploid Arabidopsis arenosa is dominated by repeated recruitment of shared alleles |
title_sort | parallel adaptation in autopolyploid arabidopsis arenosa is dominated by repeated recruitment of shared alleles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370997/ https://www.ncbi.nlm.nih.gov/pubmed/34404804 http://dx.doi.org/10.1038/s41467-021-25256-5 |
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