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Evolutionary walks through flower colour space driven by gene expression in Petunia and allies (Petunieae)

The structure and function of biochemical and developmental pathways determine the range of accessible phenotypes, which are the substrate for evolutionary change. Accordingly, we expect that observed phenotypic variation across species is strongly influenced by pathway structure, with different phe...

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Autores principales: Wheeler, Lucas C., Dunbar-Wallis, Amy, Schutz, Kyle, Smith, Stacey D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320354/
https://www.ncbi.nlm.nih.gov/pubmed/37403504
http://dx.doi.org/10.1098/rspb.2023.0275
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author Wheeler, Lucas C.
Dunbar-Wallis, Amy
Schutz, Kyle
Smith, Stacey D.
author_facet Wheeler, Lucas C.
Dunbar-Wallis, Amy
Schutz, Kyle
Smith, Stacey D.
author_sort Wheeler, Lucas C.
collection PubMed
description The structure and function of biochemical and developmental pathways determine the range of accessible phenotypes, which are the substrate for evolutionary change. Accordingly, we expect that observed phenotypic variation across species is strongly influenced by pathway structure, with different phenotypes arising due to changes in activity along pathway branches. Here, we use flower colour as a model to investigate how the structure of pigment pathways shapes the evolution of phenotypic diversity. We focus on the phenotypically diverse Petunieae clade in the nightshade family, which contains ca 180 species of Petunia and related genera, as a model to understand how flavonoid pathway gene expression maps onto pigment production. We use multivariate comparative methods to estimate co-expression relationships between pathway enzymes and transcriptional regulators, and then assess how expression of these genes relates to the major axes of variation in floral pigmentation. Our results indicate that coordinated shifts in gene expression predict transitions in both total anthocyanin levels and pigment type, which, in turn, incur trade-offs with the production of UV-absorbing flavonol compounds. These findings demonstrate that the intrinsic structure of the flavonoid pathway and its regulatory architecture underlies the accessibility of pigment phenotypes and shapes evolutionary outcomes for floral pigment production.
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spelling pubmed-103203542023-07-06 Evolutionary walks through flower colour space driven by gene expression in Petunia and allies (Petunieae) Wheeler, Lucas C. Dunbar-Wallis, Amy Schutz, Kyle Smith, Stacey D. Proc Biol Sci Evolution The structure and function of biochemical and developmental pathways determine the range of accessible phenotypes, which are the substrate for evolutionary change. Accordingly, we expect that observed phenotypic variation across species is strongly influenced by pathway structure, with different phenotypes arising due to changes in activity along pathway branches. Here, we use flower colour as a model to investigate how the structure of pigment pathways shapes the evolution of phenotypic diversity. We focus on the phenotypically diverse Petunieae clade in the nightshade family, which contains ca 180 species of Petunia and related genera, as a model to understand how flavonoid pathway gene expression maps onto pigment production. We use multivariate comparative methods to estimate co-expression relationships between pathway enzymes and transcriptional regulators, and then assess how expression of these genes relates to the major axes of variation in floral pigmentation. Our results indicate that coordinated shifts in gene expression predict transitions in both total anthocyanin levels and pigment type, which, in turn, incur trade-offs with the production of UV-absorbing flavonol compounds. These findings demonstrate that the intrinsic structure of the flavonoid pathway and its regulatory architecture underlies the accessibility of pigment phenotypes and shapes evolutionary outcomes for floral pigment production. The Royal Society 2023-07-12 2023-07-05 /pmc/articles/PMC10320354/ /pubmed/37403504 http://dx.doi.org/10.1098/rspb.2023.0275 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Wheeler, Lucas C.
Dunbar-Wallis, Amy
Schutz, Kyle
Smith, Stacey D.
Evolutionary walks through flower colour space driven by gene expression in Petunia and allies (Petunieae)
title Evolutionary walks through flower colour space driven by gene expression in Petunia and allies (Petunieae)
title_full Evolutionary walks through flower colour space driven by gene expression in Petunia and allies (Petunieae)
title_fullStr Evolutionary walks through flower colour space driven by gene expression in Petunia and allies (Petunieae)
title_full_unstemmed Evolutionary walks through flower colour space driven by gene expression in Petunia and allies (Petunieae)
title_short Evolutionary walks through flower colour space driven by gene expression in Petunia and allies (Petunieae)
title_sort evolutionary walks through flower colour space driven by gene expression in petunia and allies (petunieae)
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320354/
https://www.ncbi.nlm.nih.gov/pubmed/37403504
http://dx.doi.org/10.1098/rspb.2023.0275
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