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Pigmentation Pathway Evolution after Whole-Genome Duplication in Fish
Whole-genome duplications (WGDs) have occurred repeatedly in the vertebrate lineage, but their evolutionary significance for phenotypic evolution remains elusive. Here, we have investigated the impact of the fish-specific genome duplication (FSGD) on the evolution of pigmentation pathways in teleost...
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839281/ https://www.ncbi.nlm.nih.gov/pubmed/20333216 http://dx.doi.org/10.1093/gbe/evp050 |
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author | Braasch, Ingo Brunet, Frédéric Volff, Jean-Nicolas Schartl, Manfred |
author_facet | Braasch, Ingo Brunet, Frédéric Volff, Jean-Nicolas Schartl, Manfred |
author_sort | Braasch, Ingo |
collection | PubMed |
description | Whole-genome duplications (WGDs) have occurred repeatedly in the vertebrate lineage, but their evolutionary significance for phenotypic evolution remains elusive. Here, we have investigated the impact of the fish-specific genome duplication (FSGD) on the evolution of pigmentation pathways in teleost fishes. Pigmentation and color patterning are among the most diverse traits in teleosts, and their pigmentary system is the most complex of all vertebrate groups. Using a comparative genomic approach including phylogenetic and synteny analyses, the evolution of 128 vertebrate pigmentation genes in five teleost genomes following the FSGD has been reconstructed. We show that pigmentation genes have been preferentially retained in duplicate after the FSGD, so that teleosts have 30% more pigmentation genes compared with tetrapods. This is significantly higher than genome-wide estimates of FSGD gene duplicate retention in teleosts. Large parts of the melanocyte regulatory network have been retained in two copies after the FSGD. Duplicated pigmentation genes follow general evolutionary patterns such as the preservation of protein complex stoichiometries and the overrepresentation of developmental genes among retained duplicates. These results suggest that the FSGD has made an important contribution to the evolution of teleost-specific features of pigmentation, which include novel pigment cell types or the division of existing pigment cell types into distinct subtypes. Furthermore, we have observed species-specific differences in duplicate retention and evolution that might contribute to pigmentary diversity among teleosts. Our study therefore strongly supports the hypothesis that WGDs have promoted the increase of complexity and diversity during vertebrate phenotypic evolution. |
format | Text |
id | pubmed-2839281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28392812010-03-22 Pigmentation Pathway Evolution after Whole-Genome Duplication in Fish Braasch, Ingo Brunet, Frédéric Volff, Jean-Nicolas Schartl, Manfred Genome Biol Evol Research Articles Whole-genome duplications (WGDs) have occurred repeatedly in the vertebrate lineage, but their evolutionary significance for phenotypic evolution remains elusive. Here, we have investigated the impact of the fish-specific genome duplication (FSGD) on the evolution of pigmentation pathways in teleost fishes. Pigmentation and color patterning are among the most diverse traits in teleosts, and their pigmentary system is the most complex of all vertebrate groups. Using a comparative genomic approach including phylogenetic and synteny analyses, the evolution of 128 vertebrate pigmentation genes in five teleost genomes following the FSGD has been reconstructed. We show that pigmentation genes have been preferentially retained in duplicate after the FSGD, so that teleosts have 30% more pigmentation genes compared with tetrapods. This is significantly higher than genome-wide estimates of FSGD gene duplicate retention in teleosts. Large parts of the melanocyte regulatory network have been retained in two copies after the FSGD. Duplicated pigmentation genes follow general evolutionary patterns such as the preservation of protein complex stoichiometries and the overrepresentation of developmental genes among retained duplicates. These results suggest that the FSGD has made an important contribution to the evolution of teleost-specific features of pigmentation, which include novel pigment cell types or the division of existing pigment cell types into distinct subtypes. Furthermore, we have observed species-specific differences in duplicate retention and evolution that might contribute to pigmentary diversity among teleosts. Our study therefore strongly supports the hypothesis that WGDs have promoted the increase of complexity and diversity during vertebrate phenotypic evolution. Oxford University Press 2009 2009-11-25 /pmc/articles/PMC2839281/ /pubmed/20333216 http://dx.doi.org/10.1093/gbe/evp050 Text en © The Author(s) 2009. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Braasch, Ingo Brunet, Frédéric Volff, Jean-Nicolas Schartl, Manfred Pigmentation Pathway Evolution after Whole-Genome Duplication in Fish |
title | Pigmentation Pathway Evolution after Whole-Genome Duplication in
Fish |
title_full | Pigmentation Pathway Evolution after Whole-Genome Duplication in
Fish |
title_fullStr | Pigmentation Pathway Evolution after Whole-Genome Duplication in
Fish |
title_full_unstemmed | Pigmentation Pathway Evolution after Whole-Genome Duplication in
Fish |
title_short | Pigmentation Pathway Evolution after Whole-Genome Duplication in
Fish |
title_sort | pigmentation pathway evolution after whole-genome duplication in
fish |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839281/ https://www.ncbi.nlm.nih.gov/pubmed/20333216 http://dx.doi.org/10.1093/gbe/evp050 |
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