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Did genome duplication drive the origin of teleosts? A comparative study of diversification in ray-finned fishes

BACKGROUND: One of the main explanations for the stunning diversity of teleost fishes (~29,000 species, nearly half of all vertebrates) is that a fish-specific whole-genome duplication event (FSGD) in the ancestor to teleosts triggered their subsequent radiation. However, one critical assumption of...

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Autores principales: Santini, Francesco, Harmon, Luke J, Carnevale, Giorgio, Alfaro, Michael E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743667/
https://www.ncbi.nlm.nih.gov/pubmed/19664233
http://dx.doi.org/10.1186/1471-2148-9-194
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author Santini, Francesco
Harmon, Luke J
Carnevale, Giorgio
Alfaro, Michael E
author_facet Santini, Francesco
Harmon, Luke J
Carnevale, Giorgio
Alfaro, Michael E
author_sort Santini, Francesco
collection PubMed
description BACKGROUND: One of the main explanations for the stunning diversity of teleost fishes (~29,000 species, nearly half of all vertebrates) is that a fish-specific whole-genome duplication event (FSGD) in the ancestor to teleosts triggered their subsequent radiation. However, one critical assumption of this hypothesis, that diversification rates in teleosts increased soon after the acquisition of a duplicated genome, has never been tested. RESULTS: Here we show that one of three major diversification rate shifts within ray-finned fishes occurred at the base of the teleost radiation, as predicted by the FSGD hypothesis. We also find evidence for two rate increases that are much younger than the inferred age of the FSGD: one in the common ancestor of most ostariophysan fishes, and a second one in the common ancestor of percomorphs. The biodiversity contained within these two clades accounts for more than 88% of living fish species. CONCLUSION: Teleosts diversified explosively in their early history and this burst of diversification may have been caused by genome duplication. However, the FSGD itself may be responsible for a little over 10% of living teleost biodiversity. ~88% of species diversity is derived from two relatively recent radiations of freshwater and marine fishes where genome duplication is not suspected. Genome duplications are a common event on the tree of life and have been implicated in the diversification of major clades like flowering plants, vertebrates, and gnathostomes. However our results suggest that the causes of diversification in large clades are likely to be complex and not easily ascribed to a single event, even a dramatic one such as a whole genome duplication.
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spelling pubmed-27436672009-09-15 Did genome duplication drive the origin of teleosts? A comparative study of diversification in ray-finned fishes Santini, Francesco Harmon, Luke J Carnevale, Giorgio Alfaro, Michael E BMC Evol Biol Research Article BACKGROUND: One of the main explanations for the stunning diversity of teleost fishes (~29,000 species, nearly half of all vertebrates) is that a fish-specific whole-genome duplication event (FSGD) in the ancestor to teleosts triggered their subsequent radiation. However, one critical assumption of this hypothesis, that diversification rates in teleosts increased soon after the acquisition of a duplicated genome, has never been tested. RESULTS: Here we show that one of three major diversification rate shifts within ray-finned fishes occurred at the base of the teleost radiation, as predicted by the FSGD hypothesis. We also find evidence for two rate increases that are much younger than the inferred age of the FSGD: one in the common ancestor of most ostariophysan fishes, and a second one in the common ancestor of percomorphs. The biodiversity contained within these two clades accounts for more than 88% of living fish species. CONCLUSION: Teleosts diversified explosively in their early history and this burst of diversification may have been caused by genome duplication. However, the FSGD itself may be responsible for a little over 10% of living teleost biodiversity. ~88% of species diversity is derived from two relatively recent radiations of freshwater and marine fishes where genome duplication is not suspected. Genome duplications are a common event on the tree of life and have been implicated in the diversification of major clades like flowering plants, vertebrates, and gnathostomes. However our results suggest that the causes of diversification in large clades are likely to be complex and not easily ascribed to a single event, even a dramatic one such as a whole genome duplication. BioMed Central 2009-08-08 /pmc/articles/PMC2743667/ /pubmed/19664233 http://dx.doi.org/10.1186/1471-2148-9-194 Text en Copyright © 2009 Santini 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
Santini, Francesco
Harmon, Luke J
Carnevale, Giorgio
Alfaro, Michael E
Did genome duplication drive the origin of teleosts? A comparative study of diversification in ray-finned fishes
title Did genome duplication drive the origin of teleosts? A comparative study of diversification in ray-finned fishes
title_full Did genome duplication drive the origin of teleosts? A comparative study of diversification in ray-finned fishes
title_fullStr Did genome duplication drive the origin of teleosts? A comparative study of diversification in ray-finned fishes
title_full_unstemmed Did genome duplication drive the origin of teleosts? A comparative study of diversification in ray-finned fishes
title_short Did genome duplication drive the origin of teleosts? A comparative study of diversification in ray-finned fishes
title_sort did genome duplication drive the origin of teleosts? a comparative study of diversification in ray-finned fishes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743667/
https://www.ncbi.nlm.nih.gov/pubmed/19664233
http://dx.doi.org/10.1186/1471-2148-9-194
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