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Genetic architecture of adaptive radiation across two trophic levels
Evolution of trophic diversity is a hallmark of adaptive radiation. Yet, transitions between carnivory and herbivory are rare in young adaptive radiations. Haplochromine cichlid fish of the African Great Lakes are exceptional in this regard. Lake Victoria was colonized by an insectivorous generalist...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065965/ https://www.ncbi.nlm.nih.gov/pubmed/35506225 http://dx.doi.org/10.1098/rspb.2022.0377 |
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author | Feller, Anna F. Seehausen, Ole |
author_facet | Feller, Anna F. Seehausen, Ole |
author_sort | Feller, Anna F. |
collection | PubMed |
description | Evolution of trophic diversity is a hallmark of adaptive radiation. Yet, transitions between carnivory and herbivory are rare in young adaptive radiations. Haplochromine cichlid fish of the African Great Lakes are exceptional in this regard. Lake Victoria was colonized by an insectivorous generalist and in less than 20 000 years, several clades of specialized herbivores evolved. Carnivorous versus herbivorous lifestyles in cichlids require many different adaptations in functional morphology, physiology and behaviour. Ecological transitions in either direction thus require many traits to change in a concerted fashion, which could be facilitated if genomic regions underlying these traits were physically linked or pleiotropic. However, linkage/pleiotropy could also constrain evolvability. To investigate components of the genetic architecture of a suite of traits that distinguish invertivores from algae scrapers, we performed quantitative trait locus (QTL) mapping using a second-generation hybrid cross. While we found indications of linkage/pleiotropy within trait complexes, QTLs for distinct traits were distributed across several unlinked genomic regions. Thus, a mixture of independently segregating variation and some pleiotropy may underpin the rapid trophic transitions. We argue that the emergence and maintenance of associations between the different genomic regions underpinning co-adapted traits that evolved and persist against some gene flow required reproductive isolation. |
format | Online Article Text |
id | pubmed-9065965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90659652022-05-18 Genetic architecture of adaptive radiation across two trophic levels Feller, Anna F. Seehausen, Ole Proc Biol Sci Evolution Evolution of trophic diversity is a hallmark of adaptive radiation. Yet, transitions between carnivory and herbivory are rare in young adaptive radiations. Haplochromine cichlid fish of the African Great Lakes are exceptional in this regard. Lake Victoria was colonized by an insectivorous generalist and in less than 20 000 years, several clades of specialized herbivores evolved. Carnivorous versus herbivorous lifestyles in cichlids require many different adaptations in functional morphology, physiology and behaviour. Ecological transitions in either direction thus require many traits to change in a concerted fashion, which could be facilitated if genomic regions underlying these traits were physically linked or pleiotropic. However, linkage/pleiotropy could also constrain evolvability. To investigate components of the genetic architecture of a suite of traits that distinguish invertivores from algae scrapers, we performed quantitative trait locus (QTL) mapping using a second-generation hybrid cross. While we found indications of linkage/pleiotropy within trait complexes, QTLs for distinct traits were distributed across several unlinked genomic regions. Thus, a mixture of independently segregating variation and some pleiotropy may underpin the rapid trophic transitions. We argue that the emergence and maintenance of associations between the different genomic regions underpinning co-adapted traits that evolved and persist against some gene flow required reproductive isolation. The Royal Society 2022-05-11 2022-05-04 /pmc/articles/PMC9065965/ /pubmed/35506225 http://dx.doi.org/10.1098/rspb.2022.0377 Text en © 2022 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 Feller, Anna F. Seehausen, Ole Genetic architecture of adaptive radiation across two trophic levels |
title | Genetic architecture of adaptive radiation across two trophic levels |
title_full | Genetic architecture of adaptive radiation across two trophic levels |
title_fullStr | Genetic architecture of adaptive radiation across two trophic levels |
title_full_unstemmed | Genetic architecture of adaptive radiation across two trophic levels |
title_short | Genetic architecture of adaptive radiation across two trophic levels |
title_sort | genetic architecture of adaptive radiation across two trophic levels |
topic | Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065965/ https://www.ncbi.nlm.nih.gov/pubmed/35506225 http://dx.doi.org/10.1098/rspb.2022.0377 |
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