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A polygenic architecture with habitat‐dependent effects underlies ecological differentiation in Silene

Ecological differentiation can drive speciation but it is unclear how the genetic architecture of habitat‐dependent fitness contributes to lineage divergence. We investigated the genetic architecture of cumulative flowering, a fitness component, in second‐generation hybrids between Silene dioica and...

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Autores principales: Gramlich, Susanne, Liu, Xiaodong, Favre, Adrien, Buerkle, C. Alex, Karrenberg, Sophie
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/PMC9544174/
https://www.ncbi.nlm.nih.gov/pubmed/35586969
http://dx.doi.org/10.1111/nph.18260
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author Gramlich, Susanne
Liu, Xiaodong
Favre, Adrien
Buerkle, C. Alex
Karrenberg, Sophie
author_facet Gramlich, Susanne
Liu, Xiaodong
Favre, Adrien
Buerkle, C. Alex
Karrenberg, Sophie
author_sort Gramlich, Susanne
collection PubMed
description Ecological differentiation can drive speciation but it is unclear how the genetic architecture of habitat‐dependent fitness contributes to lineage divergence. We investigated the genetic architecture of cumulative flowering, a fitness component, in second‐generation hybrids between Silene dioica and Silene latifolia transplanted into the natural habitat of each species. We used reduced‐representation sequencing and Bayesian sparse linear mixed models (BSLMMs) to analyze the genetic control of cumulative flowering in each habitat. Our results point to a polygenic architecture of cumulative flowering. Allelic effects were mostly beneficial or deleterious in one habitat and neutral in the other. Positive‐effect alleles often were derived from the native species, whereas negative‐effect alleles, at other loci, tended to originate from the non‐native species. We conclude that ecological differentiation is governed and maintained by many loci with small, habitat‐dependent effects consistent with conditional neutrality. This pattern may result from differences in selection targets in the two habitats and from environmentally dependent deleterious load. Our results further suggest that selection for native alleles and against non‐native alleles acts as a barrier to gene flow between species.
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spelling pubmed-95441742022-10-14 A polygenic architecture with habitat‐dependent effects underlies ecological differentiation in Silene Gramlich, Susanne Liu, Xiaodong Favre, Adrien Buerkle, C. Alex Karrenberg, Sophie New Phytol Research Ecological differentiation can drive speciation but it is unclear how the genetic architecture of habitat‐dependent fitness contributes to lineage divergence. We investigated the genetic architecture of cumulative flowering, a fitness component, in second‐generation hybrids between Silene dioica and Silene latifolia transplanted into the natural habitat of each species. We used reduced‐representation sequencing and Bayesian sparse linear mixed models (BSLMMs) to analyze the genetic control of cumulative flowering in each habitat. Our results point to a polygenic architecture of cumulative flowering. Allelic effects were mostly beneficial or deleterious in one habitat and neutral in the other. Positive‐effect alleles often were derived from the native species, whereas negative‐effect alleles, at other loci, tended to originate from the non‐native species. We conclude that ecological differentiation is governed and maintained by many loci with small, habitat‐dependent effects consistent with conditional neutrality. This pattern may result from differences in selection targets in the two habitats and from environmentally dependent deleterious load. Our results further suggest that selection for native alleles and against non‐native alleles acts as a barrier to gene flow between species. John Wiley and Sons Inc. 2022-06-23 2022-08 /pmc/articles/PMC9544174/ /pubmed/35586969 http://dx.doi.org/10.1111/nph.18260 Text en © 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research
Gramlich, Susanne
Liu, Xiaodong
Favre, Adrien
Buerkle, C. Alex
Karrenberg, Sophie
A polygenic architecture with habitat‐dependent effects underlies ecological differentiation in Silene
title A polygenic architecture with habitat‐dependent effects underlies ecological differentiation in Silene
title_full A polygenic architecture with habitat‐dependent effects underlies ecological differentiation in Silene
title_fullStr A polygenic architecture with habitat‐dependent effects underlies ecological differentiation in Silene
title_full_unstemmed A polygenic architecture with habitat‐dependent effects underlies ecological differentiation in Silene
title_short A polygenic architecture with habitat‐dependent effects underlies ecological differentiation in Silene
title_sort polygenic architecture with habitat‐dependent effects underlies ecological differentiation in silene
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544174/
https://www.ncbi.nlm.nih.gov/pubmed/35586969
http://dx.doi.org/10.1111/nph.18260
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