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Evolution of cichlid vision via trans-regulatory divergence

BACKGROUND: Phenotypic evolution may occur through mutations that affect either the structure or expression of protein-coding genes. Although the evolution of color vision has historically been attributed to structural mutations within the opsin genes, recent research has shown that opsin regulatory...

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Autores principales: O’Quin, Kelly E, Schulte, Jane E, Patel, Zil, Kahn, Nadia, Naseer, Zan, Wang, Helena, Conte, Matthew A, Carleton, Karen L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575402/
https://www.ncbi.nlm.nih.gov/pubmed/23267665
http://dx.doi.org/10.1186/1471-2148-12-251
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author O’Quin, Kelly E
Schulte, Jane E
Patel, Zil
Kahn, Nadia
Naseer, Zan
Wang, Helena
Conte, Matthew A
Carleton, Karen L
author_facet O’Quin, Kelly E
Schulte, Jane E
Patel, Zil
Kahn, Nadia
Naseer, Zan
Wang, Helena
Conte, Matthew A
Carleton, Karen L
author_sort O’Quin, Kelly E
collection PubMed
description BACKGROUND: Phenotypic evolution may occur through mutations that affect either the structure or expression of protein-coding genes. Although the evolution of color vision has historically been attributed to structural mutations within the opsin genes, recent research has shown that opsin regulatory mutations can also tune photoreceptor sensitivity and color vision. Visual sensitivity in African cichlid fishes varies as a result of the differential expression of seven opsin genes. We crossed cichlid species that express different opsin gene sets and scanned their genome for expression Quantitative Trait Loci (eQTL) responsible for these differences. Our results shed light on the role that different structural, cis-, and trans-regulatory mutations play in the evolution of color vision. RESULTS: We identified 11 eQTL that contribute to the divergent expression of five opsin genes. On three linkage groups, several eQTL formed regulatory “hotspots” associated with the expression of multiple opsins. Importantly, however, the majority of the eQTL we identified (8/11 or 73%) occur on linkage groups located trans to the opsin genes, suggesting that cichlid color vision has evolved primarily via trans-regulatory divergence. By modeling the impact of just two of these trans-regulatory eQTL, we show that opsin regulatory mutations can alter cichlid photoreceptor sensitivity and color vision at least as much as opsin structural mutations can. CONCLUSIONS: Combined with previous work, we demonstrate that the evolution of cichlid color vision results from the interplay of structural, cis-, and especially trans-regulatory loci. Although there are numerous examples of structural and cis-regulatory mutations that contribute to phenotypic evolution, our results suggest that trans-regulatory mutations could contribute to phenotypic divergence more commonly than previously expected, especially in systems like color vision, where compensatory changes in the expression of multiple genes are required in order to produce functional phenotypes.
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spelling pubmed-35754022013-02-19 Evolution of cichlid vision via trans-regulatory divergence O’Quin, Kelly E Schulte, Jane E Patel, Zil Kahn, Nadia Naseer, Zan Wang, Helena Conte, Matthew A Carleton, Karen L BMC Evol Biol Research Article BACKGROUND: Phenotypic evolution may occur through mutations that affect either the structure or expression of protein-coding genes. Although the evolution of color vision has historically been attributed to structural mutations within the opsin genes, recent research has shown that opsin regulatory mutations can also tune photoreceptor sensitivity and color vision. Visual sensitivity in African cichlid fishes varies as a result of the differential expression of seven opsin genes. We crossed cichlid species that express different opsin gene sets and scanned their genome for expression Quantitative Trait Loci (eQTL) responsible for these differences. Our results shed light on the role that different structural, cis-, and trans-regulatory mutations play in the evolution of color vision. RESULTS: We identified 11 eQTL that contribute to the divergent expression of five opsin genes. On three linkage groups, several eQTL formed regulatory “hotspots” associated with the expression of multiple opsins. Importantly, however, the majority of the eQTL we identified (8/11 or 73%) occur on linkage groups located trans to the opsin genes, suggesting that cichlid color vision has evolved primarily via trans-regulatory divergence. By modeling the impact of just two of these trans-regulatory eQTL, we show that opsin regulatory mutations can alter cichlid photoreceptor sensitivity and color vision at least as much as opsin structural mutations can. CONCLUSIONS: Combined with previous work, we demonstrate that the evolution of cichlid color vision results from the interplay of structural, cis-, and especially trans-regulatory loci. Although there are numerous examples of structural and cis-regulatory mutations that contribute to phenotypic evolution, our results suggest that trans-regulatory mutations could contribute to phenotypic divergence more commonly than previously expected, especially in systems like color vision, where compensatory changes in the expression of multiple genes are required in order to produce functional phenotypes. BioMed Central 2012-12-26 /pmc/articles/PMC3575402/ /pubmed/23267665 http://dx.doi.org/10.1186/1471-2148-12-251 Text en Copyright ©2012 O'Quin et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
O’Quin, Kelly E
Schulte, Jane E
Patel, Zil
Kahn, Nadia
Naseer, Zan
Wang, Helena
Conte, Matthew A
Carleton, Karen L
Evolution of cichlid vision via trans-regulatory divergence
title Evolution of cichlid vision via trans-regulatory divergence
title_full Evolution of cichlid vision via trans-regulatory divergence
title_fullStr Evolution of cichlid vision via trans-regulatory divergence
title_full_unstemmed Evolution of cichlid vision via trans-regulatory divergence
title_short Evolution of cichlid vision via trans-regulatory divergence
title_sort evolution of cichlid vision via trans-regulatory divergence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575402/
https://www.ncbi.nlm.nih.gov/pubmed/23267665
http://dx.doi.org/10.1186/1471-2148-12-251
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