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Extensive Local Gene Duplication and Functional Divergence among Paralogs in Atlantic Salmon

Many organisms can generate alternative phenotypes from the same genome, enabling individuals to exploit diverse and variable environments. A prevailing hypothesis is that such adaptation has been favored by gene duplication events, which generate redundant genomic material that may evolve divergent...

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Autores principales: Warren, Ian A., Ciborowski, Kate L., Casadei, Elisa, Hazlerigg, David G., Martin, Sam, Jordan, William C., Sumner, Seirian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122929/
https://www.ncbi.nlm.nih.gov/pubmed/24951567
http://dx.doi.org/10.1093/gbe/evu131
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author Warren, Ian A.
Ciborowski, Kate L.
Casadei, Elisa
Hazlerigg, David G.
Martin, Sam
Jordan, William C.
Sumner, Seirian
author_facet Warren, Ian A.
Ciborowski, Kate L.
Casadei, Elisa
Hazlerigg, David G.
Martin, Sam
Jordan, William C.
Sumner, Seirian
author_sort Warren, Ian A.
collection PubMed
description Many organisms can generate alternative phenotypes from the same genome, enabling individuals to exploit diverse and variable environments. A prevailing hypothesis is that such adaptation has been favored by gene duplication events, which generate redundant genomic material that may evolve divergent functions. Vertebrate examples of recent whole-genome duplications are sparse although one example is the salmonids, which have undergone a whole-genome duplication event within the last 100 Myr. The life-cycle of the Atlantic salmon, Salmo salar, depends on the ability to produce alternating phenotypes from the same genome, to facilitate migration and maintain its anadromous life history. Here, we investigate the hypothesis that genome-wide and local gene duplication events have contributed to the salmonid adaptation. We used high-throughput sequencing to characterize the transcriptomes of three key organs involved in regulating migration in S. salar: Brain, pituitary, and olfactory epithelium. We identified over 10,000 undescribed S. salar sequences and designed an analytic workflow to distinguish between paralogs originating from local gene duplication events or from whole-genome duplication events. These data reveal that substantial local gene duplications took place shortly after the whole-genome duplication event. Many of the identified paralog pairs have either diverged in function or become noncoding. Future functional genomics studies will reveal to what extent this rich source of divergence in genetic sequence is likely to have facilitated the evolution of extreme phenotypic plasticity required for an anadromous life-cycle.
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spelling pubmed-41229292014-08-12 Extensive Local Gene Duplication and Functional Divergence among Paralogs in Atlantic Salmon Warren, Ian A. Ciborowski, Kate L. Casadei, Elisa Hazlerigg, David G. Martin, Sam Jordan, William C. Sumner, Seirian Genome Biol Evol Research Article Many organisms can generate alternative phenotypes from the same genome, enabling individuals to exploit diverse and variable environments. A prevailing hypothesis is that such adaptation has been favored by gene duplication events, which generate redundant genomic material that may evolve divergent functions. Vertebrate examples of recent whole-genome duplications are sparse although one example is the salmonids, which have undergone a whole-genome duplication event within the last 100 Myr. The life-cycle of the Atlantic salmon, Salmo salar, depends on the ability to produce alternating phenotypes from the same genome, to facilitate migration and maintain its anadromous life history. Here, we investigate the hypothesis that genome-wide and local gene duplication events have contributed to the salmonid adaptation. We used high-throughput sequencing to characterize the transcriptomes of three key organs involved in regulating migration in S. salar: Brain, pituitary, and olfactory epithelium. We identified over 10,000 undescribed S. salar sequences and designed an analytic workflow to distinguish between paralogs originating from local gene duplication events or from whole-genome duplication events. These data reveal that substantial local gene duplications took place shortly after the whole-genome duplication event. Many of the identified paralog pairs have either diverged in function or become noncoding. Future functional genomics studies will reveal to what extent this rich source of divergence in genetic sequence is likely to have facilitated the evolution of extreme phenotypic plasticity required for an anadromous life-cycle. Oxford University Press 2014-06-19 /pmc/articles/PMC4122929/ /pubmed/24951567 http://dx.doi.org/10.1093/gbe/evu131 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Warren, Ian A.
Ciborowski, Kate L.
Casadei, Elisa
Hazlerigg, David G.
Martin, Sam
Jordan, William C.
Sumner, Seirian
Extensive Local Gene Duplication and Functional Divergence among Paralogs in Atlantic Salmon
title Extensive Local Gene Duplication and Functional Divergence among Paralogs in Atlantic Salmon
title_full Extensive Local Gene Duplication and Functional Divergence among Paralogs in Atlantic Salmon
title_fullStr Extensive Local Gene Duplication and Functional Divergence among Paralogs in Atlantic Salmon
title_full_unstemmed Extensive Local Gene Duplication and Functional Divergence among Paralogs in Atlantic Salmon
title_short Extensive Local Gene Duplication and Functional Divergence among Paralogs in Atlantic Salmon
title_sort extensive local gene duplication and functional divergence among paralogs in atlantic salmon
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122929/
https://www.ncbi.nlm.nih.gov/pubmed/24951567
http://dx.doi.org/10.1093/gbe/evu131
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