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Evolution of pigment synthesis pathways by gene and genome duplication in fish

BACKGROUND: Coloration and color patterning belong to the most diverse phenotypic traits in animals. Particularly, teleost fishes possess more pigment cell types than any other group of vertebrates. As the result of an ancient fish-specific genome duplication (FSGD), teleost genomes might contain mo...

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Autores principales: Braasch, Ingo, Schartl, Manfred, Volff, Jean-Nicolas
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1890551/
https://www.ncbi.nlm.nih.gov/pubmed/17498288
http://dx.doi.org/10.1186/1471-2148-7-74
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author Braasch, Ingo
Schartl, Manfred
Volff, Jean-Nicolas
author_facet Braasch, Ingo
Schartl, Manfred
Volff, Jean-Nicolas
author_sort Braasch, Ingo
collection PubMed
description BACKGROUND: Coloration and color patterning belong to the most diverse phenotypic traits in animals. Particularly, teleost fishes possess more pigment cell types than any other group of vertebrates. As the result of an ancient fish-specific genome duplication (FSGD), teleost genomes might contain more copies of genes involved in pigment cell development than tetrapods. No systematic genomic inventory allowing to test this hypothesis has been drawn up so far for pigmentation genes in fish, and almost nothing is known about the evolution of these genes in different fish lineages. RESULTS: Using a comparative genomic approach including phylogenetic reconstructions and synteny analyses, we have studied two major pigment synthesis pathways in teleost fish, the melanin and the pteridine pathways, with respect to different types of gene duplication. Genes encoding three of the four enzymes involved in the synthesis of melanin from tyrosine have been retained as duplicates after the FSGD. In the pteridine pathway, two cases of duplicated genes originating from the FSGD as well as several lineage-specific gene duplications were observed. In both pathways, genes encoding the rate-limiting enzymes, tyrosinase and GTP-cyclohydrolase I (GchI), have additional paralogs in teleosts compared to tetrapods, which have been generated by different modes of duplication. We have also observed a previously unrecognized diversity of gchI genes in vertebrates. In addition, we have found evidence for divergent resolution of duplicated pigmentation genes, i.e., differential gene loss in divergent teleost lineages, particularly in the tyrosinase gene family. CONCLUSION: Mainly due to the FSGD, teleost fishes apparently have a greater repertoire of pigment synthesis genes than any other vertebrate group. Our results support an important role of the FSGD and other types of duplication in the evolution of pigmentation in fish.
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spelling pubmed-18905512007-06-11 Evolution of pigment synthesis pathways by gene and genome duplication in fish Braasch, Ingo Schartl, Manfred Volff, Jean-Nicolas BMC Evol Biol Research Article BACKGROUND: Coloration and color patterning belong to the most diverse phenotypic traits in animals. Particularly, teleost fishes possess more pigment cell types than any other group of vertebrates. As the result of an ancient fish-specific genome duplication (FSGD), teleost genomes might contain more copies of genes involved in pigment cell development than tetrapods. No systematic genomic inventory allowing to test this hypothesis has been drawn up so far for pigmentation genes in fish, and almost nothing is known about the evolution of these genes in different fish lineages. RESULTS: Using a comparative genomic approach including phylogenetic reconstructions and synteny analyses, we have studied two major pigment synthesis pathways in teleost fish, the melanin and the pteridine pathways, with respect to different types of gene duplication. Genes encoding three of the four enzymes involved in the synthesis of melanin from tyrosine have been retained as duplicates after the FSGD. In the pteridine pathway, two cases of duplicated genes originating from the FSGD as well as several lineage-specific gene duplications were observed. In both pathways, genes encoding the rate-limiting enzymes, tyrosinase and GTP-cyclohydrolase I (GchI), have additional paralogs in teleosts compared to tetrapods, which have been generated by different modes of duplication. We have also observed a previously unrecognized diversity of gchI genes in vertebrates. In addition, we have found evidence for divergent resolution of duplicated pigmentation genes, i.e., differential gene loss in divergent teleost lineages, particularly in the tyrosinase gene family. CONCLUSION: Mainly due to the FSGD, teleost fishes apparently have a greater repertoire of pigment synthesis genes than any other vertebrate group. Our results support an important role of the FSGD and other types of duplication in the evolution of pigmentation in fish. BioMed Central 2007-05-11 /pmc/articles/PMC1890551/ /pubmed/17498288 http://dx.doi.org/10.1186/1471-2148-7-74 Text en Copyright © 2007 Braasch 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
Braasch, Ingo
Schartl, Manfred
Volff, Jean-Nicolas
Evolution of pigment synthesis pathways by gene and genome duplication in fish
title Evolution of pigment synthesis pathways by gene and genome duplication in fish
title_full Evolution of pigment synthesis pathways by gene and genome duplication in fish
title_fullStr Evolution of pigment synthesis pathways by gene and genome duplication in fish
title_full_unstemmed Evolution of pigment synthesis pathways by gene and genome duplication in fish
title_short Evolution of pigment synthesis pathways by gene and genome duplication in fish
title_sort evolution of pigment synthesis pathways by gene and genome duplication in fish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1890551/
https://www.ncbi.nlm.nih.gov/pubmed/17498288
http://dx.doi.org/10.1186/1471-2148-7-74
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