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Cross‐kingdom transcriptomic trends in the evolution of hybrid gene expression

Hybridization is a route to speciation that occurs widely across the eukaryote tree of life. The success of allopolyploids (hybrid species with increased ploidy) and homoploid hybrids (with unchanged ploidy) is well documented. However, their formation and establishment is not straightforward, with...

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Autores principales: Behling, Anna H., Winter, David J., Ganley, Austen R. D., Cox, Murray P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546207/
https://www.ncbi.nlm.nih.gov/pubmed/35830478
http://dx.doi.org/10.1111/jeb.14059
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author Behling, Anna H.
Winter, David J.
Ganley, Austen R. D.
Cox, Murray P.
author_facet Behling, Anna H.
Winter, David J.
Ganley, Austen R. D.
Cox, Murray P.
author_sort Behling, Anna H.
collection PubMed
description Hybridization is a route to speciation that occurs widely across the eukaryote tree of life. The success of allopolyploids (hybrid species with increased ploidy) and homoploid hybrids (with unchanged ploidy) is well documented. However, their formation and establishment is not straightforward, with a suite of near‐instantaneous and longer term biological repercussions faced by the new species. Central to these challenges is the rewiring of gene regulatory networks following the merger of distinct genomes inherited from both parental species. Research on the evolution of hybrid gene expression has largely involved studies on a single hybrid species or a few gene families. Here, we present the first standardized transcriptome‐wide study exploring the fates of genes following hybridization across three kingdoms: animals, plants and fungi. Within each kingdom, we pair an allopolyploid system with a closely related homoploid hybrid to decouple the influence of increased ploidy from genome merger. Genome merger, not changes in ploidy, has the greatest effect on posthybridization expression patterns across all study systems. Strikingly, we find that differentially expressed genes in parent species preferentially switch to more similar expression in hybrids across all kingdoms, likely as a consequence of regulatory trans‐acting cross‐talk within the hybrid nucleus. We also highlight the prevalence of gene loss or silencing among extremely differentially expressed genes in hybrid species across all kingdoms. These shared patterns suggest that the evolutionary process of hybridization leads to common high‐level expression outcomes, regardless of the particular species or kingdom.
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spelling pubmed-95462072022-10-14 Cross‐kingdom transcriptomic trends in the evolution of hybrid gene expression Behling, Anna H. Winter, David J. Ganley, Austen R. D. Cox, Murray P. J Evol Biol Research Articles Hybridization is a route to speciation that occurs widely across the eukaryote tree of life. The success of allopolyploids (hybrid species with increased ploidy) and homoploid hybrids (with unchanged ploidy) is well documented. However, their formation and establishment is not straightforward, with a suite of near‐instantaneous and longer term biological repercussions faced by the new species. Central to these challenges is the rewiring of gene regulatory networks following the merger of distinct genomes inherited from both parental species. Research on the evolution of hybrid gene expression has largely involved studies on a single hybrid species or a few gene families. Here, we present the first standardized transcriptome‐wide study exploring the fates of genes following hybridization across three kingdoms: animals, plants and fungi. Within each kingdom, we pair an allopolyploid system with a closely related homoploid hybrid to decouple the influence of increased ploidy from genome merger. Genome merger, not changes in ploidy, has the greatest effect on posthybridization expression patterns across all study systems. Strikingly, we find that differentially expressed genes in parent species preferentially switch to more similar expression in hybrids across all kingdoms, likely as a consequence of regulatory trans‐acting cross‐talk within the hybrid nucleus. We also highlight the prevalence of gene loss or silencing among extremely differentially expressed genes in hybrid species across all kingdoms. These shared patterns suggest that the evolutionary process of hybridization leads to common high‐level expression outcomes, regardless of the particular species or kingdom. John Wiley and Sons Inc. 2022-07-13 2022-08 /pmc/articles/PMC9546207/ /pubmed/35830478 http://dx.doi.org/10.1111/jeb.14059 Text en © 2022 The Authors. Journal of Evolutionary Biology published by John Wiley & Sons Ltd on behalf of European Society for Evolutionary Biology. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Behling, Anna H.
Winter, David J.
Ganley, Austen R. D.
Cox, Murray P.
Cross‐kingdom transcriptomic trends in the evolution of hybrid gene expression
title Cross‐kingdom transcriptomic trends in the evolution of hybrid gene expression
title_full Cross‐kingdom transcriptomic trends in the evolution of hybrid gene expression
title_fullStr Cross‐kingdom transcriptomic trends in the evolution of hybrid gene expression
title_full_unstemmed Cross‐kingdom transcriptomic trends in the evolution of hybrid gene expression
title_short Cross‐kingdom transcriptomic trends in the evolution of hybrid gene expression
title_sort cross‐kingdom transcriptomic trends in the evolution of hybrid gene expression
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546207/
https://www.ncbi.nlm.nih.gov/pubmed/35830478
http://dx.doi.org/10.1111/jeb.14059
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