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Evolution of regulatory networks associated with traits under selection in cichlids

BACKGROUND: Seminal studies of vertebrate protein evolution speculated that gene regulatory changes can drive anatomical innovations. However, very little is known about gene regulatory network (GRN) evolution associated with phenotypic effect across ecologically diverse species. Here we use a novel...

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Autores principales: Mehta, Tarang K., Koch, Christopher, Nash, Will, Knaack, Sara A., Sudhakar, Padhmanand, Olbei, Marton, Bastkowski, Sarah, Penso-Dolfin, Luca, Korcsmaros, Tamas, Haerty, Wilfried, Roy, Sushmita, Di-Palma, Federica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791837/
https://www.ncbi.nlm.nih.gov/pubmed/33419455
http://dx.doi.org/10.1186/s13059-020-02208-8
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author Mehta, Tarang K.
Koch, Christopher
Nash, Will
Knaack, Sara A.
Sudhakar, Padhmanand
Olbei, Marton
Bastkowski, Sarah
Penso-Dolfin, Luca
Korcsmaros, Tamas
Haerty, Wilfried
Roy, Sushmita
Di-Palma, Federica
author_facet Mehta, Tarang K.
Koch, Christopher
Nash, Will
Knaack, Sara A.
Sudhakar, Padhmanand
Olbei, Marton
Bastkowski, Sarah
Penso-Dolfin, Luca
Korcsmaros, Tamas
Haerty, Wilfried
Roy, Sushmita
Di-Palma, Federica
author_sort Mehta, Tarang K.
collection PubMed
description BACKGROUND: Seminal studies of vertebrate protein evolution speculated that gene regulatory changes can drive anatomical innovations. However, very little is known about gene regulatory network (GRN) evolution associated with phenotypic effect across ecologically diverse species. Here we use a novel approach for comparative GRN analysis in vertebrate species to study GRN evolution in representative species of the most striking examples of adaptive radiations, the East African cichlids. We previously demonstrated how the explosive phenotypic diversification of East African cichlids can be attributed to diverse molecular mechanisms, including accelerated regulatory sequence evolution and gene expression divergence. RESULTS: To investigate these mechanisms across species at a genome-wide scale, we develop a novel computational pipeline that predicts regulators for co-extant and ancestral co-expression modules along a phylogeny, and candidate regulatory regions associated with traits under selection in cichlids. As a case study, we apply our approach to a well-studied adaptive trait—the visual system—for which we report striking cases of network rewiring for visual opsin genes, identify discrete regulatory variants, and investigate their association with cichlid visual system evolution. In regulatory regions of visual opsin genes, in vitro assays confirm that transcription factor binding site mutations disrupt regulatory edges across species and segregate according to lake species phylogeny and ecology, suggesting GRN rewiring in radiating cichlids. CONCLUSIONS: Our approach reveals numerous novel potential candidate regulators and regulatory regions across cichlid genomes, including some novel and some previously reported associations to known adaptive evolutionary traits.
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spelling pubmed-77918372021-01-11 Evolution of regulatory networks associated with traits under selection in cichlids Mehta, Tarang K. Koch, Christopher Nash, Will Knaack, Sara A. Sudhakar, Padhmanand Olbei, Marton Bastkowski, Sarah Penso-Dolfin, Luca Korcsmaros, Tamas Haerty, Wilfried Roy, Sushmita Di-Palma, Federica Genome Biol Research BACKGROUND: Seminal studies of vertebrate protein evolution speculated that gene regulatory changes can drive anatomical innovations. However, very little is known about gene regulatory network (GRN) evolution associated with phenotypic effect across ecologically diverse species. Here we use a novel approach for comparative GRN analysis in vertebrate species to study GRN evolution in representative species of the most striking examples of adaptive radiations, the East African cichlids. We previously demonstrated how the explosive phenotypic diversification of East African cichlids can be attributed to diverse molecular mechanisms, including accelerated regulatory sequence evolution and gene expression divergence. RESULTS: To investigate these mechanisms across species at a genome-wide scale, we develop a novel computational pipeline that predicts regulators for co-extant and ancestral co-expression modules along a phylogeny, and candidate regulatory regions associated with traits under selection in cichlids. As a case study, we apply our approach to a well-studied adaptive trait—the visual system—for which we report striking cases of network rewiring for visual opsin genes, identify discrete regulatory variants, and investigate their association with cichlid visual system evolution. In regulatory regions of visual opsin genes, in vitro assays confirm that transcription factor binding site mutations disrupt regulatory edges across species and segregate according to lake species phylogeny and ecology, suggesting GRN rewiring in radiating cichlids. CONCLUSIONS: Our approach reveals numerous novel potential candidate regulators and regulatory regions across cichlid genomes, including some novel and some previously reported associations to known adaptive evolutionary traits. BioMed Central 2021-01-08 /pmc/articles/PMC7791837/ /pubmed/33419455 http://dx.doi.org/10.1186/s13059-020-02208-8 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Mehta, Tarang K.
Koch, Christopher
Nash, Will
Knaack, Sara A.
Sudhakar, Padhmanand
Olbei, Marton
Bastkowski, Sarah
Penso-Dolfin, Luca
Korcsmaros, Tamas
Haerty, Wilfried
Roy, Sushmita
Di-Palma, Federica
Evolution of regulatory networks associated with traits under selection in cichlids
title Evolution of regulatory networks associated with traits under selection in cichlids
title_full Evolution of regulatory networks associated with traits under selection in cichlids
title_fullStr Evolution of regulatory networks associated with traits under selection in cichlids
title_full_unstemmed Evolution of regulatory networks associated with traits under selection in cichlids
title_short Evolution of regulatory networks associated with traits under selection in cichlids
title_sort evolution of regulatory networks associated with traits under selection in cichlids
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791837/
https://www.ncbi.nlm.nih.gov/pubmed/33419455
http://dx.doi.org/10.1186/s13059-020-02208-8
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