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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...

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Autores principales: Feller, Anna F., Seehausen, Ole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
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.
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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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