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Long-term balancing selection drives evolution of immunity genes in Capsella

Genetic drift is expected to remove polymorphism from populations over long periods of time, with the rate of polymorphism loss being accelerated when species experience strong reductions in population size. Adaptive forces that maintain genetic variation in populations, or balancing selection, migh...

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Autores principales: Koenig, Daniel, Hagmann, Jörg, Li, Rachel, Bemm, Felix, Slotte, Tanja, Neuffer, Barbara, Wright, Stephen I, Weigel, Detlef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426441/
https://www.ncbi.nlm.nih.gov/pubmed/30806624
http://dx.doi.org/10.7554/eLife.43606
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author Koenig, Daniel
Hagmann, Jörg
Li, Rachel
Bemm, Felix
Slotte, Tanja
Neuffer, Barbara
Wright, Stephen I
Weigel, Detlef
author_facet Koenig, Daniel
Hagmann, Jörg
Li, Rachel
Bemm, Felix
Slotte, Tanja
Neuffer, Barbara
Wright, Stephen I
Weigel, Detlef
author_sort Koenig, Daniel
collection PubMed
description Genetic drift is expected to remove polymorphism from populations over long periods of time, with the rate of polymorphism loss being accelerated when species experience strong reductions in population size. Adaptive forces that maintain genetic variation in populations, or balancing selection, might counteract this process. To understand the extent to which natural selection can drive the retention of genetic diversity, we document genomic variability after two parallel species-wide bottlenecks in the genus Capsella. We find that ancestral variation preferentially persists at immunity related loci, and that the same collection of alleles has been maintained in different lineages that have been separated for several million years. By reconstructing the evolution of the disease-related locus MLO2b, we find that divergence between ancient haplotypes can be obscured by referenced based re-sequencing methods, and that trans-specific alleles can encode substantially diverged protein sequences. Our data point to long-term balancing selection as an important factor shaping the genetics of immune systems in plants and as the predominant driver of genomic variability after a population bottleneck.
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spelling pubmed-64264412019-03-21 Long-term balancing selection drives evolution of immunity genes in Capsella Koenig, Daniel Hagmann, Jörg Li, Rachel Bemm, Felix Slotte, Tanja Neuffer, Barbara Wright, Stephen I Weigel, Detlef eLife Evolutionary Biology Genetic drift is expected to remove polymorphism from populations over long periods of time, with the rate of polymorphism loss being accelerated when species experience strong reductions in population size. Adaptive forces that maintain genetic variation in populations, or balancing selection, might counteract this process. To understand the extent to which natural selection can drive the retention of genetic diversity, we document genomic variability after two parallel species-wide bottlenecks in the genus Capsella. We find that ancestral variation preferentially persists at immunity related loci, and that the same collection of alleles has been maintained in different lineages that have been separated for several million years. By reconstructing the evolution of the disease-related locus MLO2b, we find that divergence between ancient haplotypes can be obscured by referenced based re-sequencing methods, and that trans-specific alleles can encode substantially diverged protein sequences. Our data point to long-term balancing selection as an important factor shaping the genetics of immune systems in plants and as the predominant driver of genomic variability after a population bottleneck. eLife Sciences Publications, Ltd 2019-02-26 /pmc/articles/PMC6426441/ /pubmed/30806624 http://dx.doi.org/10.7554/eLife.43606 Text en © 2019, Koenig et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Evolutionary Biology
Koenig, Daniel
Hagmann, Jörg
Li, Rachel
Bemm, Felix
Slotte, Tanja
Neuffer, Barbara
Wright, Stephen I
Weigel, Detlef
Long-term balancing selection drives evolution of immunity genes in Capsella
title Long-term balancing selection drives evolution of immunity genes in Capsella
title_full Long-term balancing selection drives evolution of immunity genes in Capsella
title_fullStr Long-term balancing selection drives evolution of immunity genes in Capsella
title_full_unstemmed Long-term balancing selection drives evolution of immunity genes in Capsella
title_short Long-term balancing selection drives evolution of immunity genes in Capsella
title_sort long-term balancing selection drives evolution of immunity genes in capsella
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426441/
https://www.ncbi.nlm.nih.gov/pubmed/30806624
http://dx.doi.org/10.7554/eLife.43606
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