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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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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. |
format | Online Article Text |
id | pubmed-9544174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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
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title_full | A polygenic architecture with habitat‐dependent effects underlies ecological differentiation in Silene
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title_fullStr | A polygenic architecture with habitat‐dependent effects underlies ecological differentiation in Silene
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title_full_unstemmed | A polygenic architecture with habitat‐dependent effects underlies ecological differentiation in Silene
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title_short | A polygenic architecture with habitat‐dependent effects underlies ecological differentiation in Silene
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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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