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Structure and contingency determine mutational hotspots for flower color evolution

Evolutionary genetic studies have uncovered abundant evidence for genomic hotspots of phenotypic evolution, as well as biased patterns of mutations at those loci. However, the theoretical basis for this concentration of particular types of mutations at particular loci remains largely unexplored. In...

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Autores principales: Wheeler, Lucas C., Wing, Boswell A., Smith, Stacey D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857289/
https://www.ncbi.nlm.nih.gov/pubmed/33552536
http://dx.doi.org/10.1002/evl3.212
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author Wheeler, Lucas C.
Wing, Boswell A.
Smith, Stacey D.
author_facet Wheeler, Lucas C.
Wing, Boswell A.
Smith, Stacey D.
author_sort Wheeler, Lucas C.
collection PubMed
description Evolutionary genetic studies have uncovered abundant evidence for genomic hotspots of phenotypic evolution, as well as biased patterns of mutations at those loci. However, the theoretical basis for this concentration of particular types of mutations at particular loci remains largely unexplored. In addition, historical contingency is known to play a major role in evolutionary trajectories, but has not been reconciled with the existence of such hotspots. For example, do the appearance of hotspots and the fixation of different types of mutations at those loci depend on the starting state and/or on the nature and direction of selection? Here, we use a computational approach to examine these questions, focusing the anthocyanin pigmentation pathway, which has been extensively studied in the context of flower color transitions. We investigate two transitions that are common in nature, the transition from blue to purple pigmentation and from purple to red pigmentation. Both sets of simulated transitions occur with a small number of mutations at just four loci and show strikingly similar peaked shapes of evolutionary trajectories, with the mutations of the largest effect occurring early but not first. Nevertheless, the types of mutations (biochemical vs. regulatory) as well as their direction and magnitude are contingent on the particular transition. These simulated color transitions largely mirror findings from natural flower color transitions, which are known to occur via repeated changes at a few hotspot loci. Still, some types of mutations observed in our simulated color evolution are rarely observed in nature, suggesting that pleiotropic effects further limit the trajectories between color phenotypes. Overall, our results indicate that the branching structure of the pathway leads to a predictable concentration of evolutionary change at the hotspot loci, but the types of mutations at these loci and their order is contingent on the evolutionary context.
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spelling pubmed-78572892021-02-05 Structure and contingency determine mutational hotspots for flower color evolution Wheeler, Lucas C. Wing, Boswell A. Smith, Stacey D. Evol Lett Letters Evolutionary genetic studies have uncovered abundant evidence for genomic hotspots of phenotypic evolution, as well as biased patterns of mutations at those loci. However, the theoretical basis for this concentration of particular types of mutations at particular loci remains largely unexplored. In addition, historical contingency is known to play a major role in evolutionary trajectories, but has not been reconciled with the existence of such hotspots. For example, do the appearance of hotspots and the fixation of different types of mutations at those loci depend on the starting state and/or on the nature and direction of selection? Here, we use a computational approach to examine these questions, focusing the anthocyanin pigmentation pathway, which has been extensively studied in the context of flower color transitions. We investigate two transitions that are common in nature, the transition from blue to purple pigmentation and from purple to red pigmentation. Both sets of simulated transitions occur with a small number of mutations at just four loci and show strikingly similar peaked shapes of evolutionary trajectories, with the mutations of the largest effect occurring early but not first. Nevertheless, the types of mutations (biochemical vs. regulatory) as well as their direction and magnitude are contingent on the particular transition. These simulated color transitions largely mirror findings from natural flower color transitions, which are known to occur via repeated changes at a few hotspot loci. Still, some types of mutations observed in our simulated color evolution are rarely observed in nature, suggesting that pleiotropic effects further limit the trajectories between color phenotypes. Overall, our results indicate that the branching structure of the pathway leads to a predictable concentration of evolutionary change at the hotspot loci, but the types of mutations at these loci and their order is contingent on the evolutionary context. John Wiley and Sons Inc. 2020-12-26 /pmc/articles/PMC7857289/ /pubmed/33552536 http://dx.doi.org/10.1002/evl3.212 Text en © 2020 The Authors. Evolution Letters published by Wiley Periodicals, LLC on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB). This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters
Wheeler, Lucas C.
Wing, Boswell A.
Smith, Stacey D.
Structure and contingency determine mutational hotspots for flower color evolution
title Structure and contingency determine mutational hotspots for flower color evolution
title_full Structure and contingency determine mutational hotspots for flower color evolution
title_fullStr Structure and contingency determine mutational hotspots for flower color evolution
title_full_unstemmed Structure and contingency determine mutational hotspots for flower color evolution
title_short Structure and contingency determine mutational hotspots for flower color evolution
title_sort structure and contingency determine mutational hotspots for flower color evolution
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857289/
https://www.ncbi.nlm.nih.gov/pubmed/33552536
http://dx.doi.org/10.1002/evl3.212
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