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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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.
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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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