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Positive selection in the adhesion domain of Mus sperm Adam genes through gene duplications and function-driven gene complex formations

BACKGROUND: Sperm and testes-expressed Adam genes have been shown to undergo bouts of positive selection in mammals. Despite the pervasiveness of positive selection signals, it is unclear what has driven such selective bouts. The fact that only sperm surface Adam genes show signals of positive selec...

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Autores principales: Grayson, Phil, Civetta, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3849967/
https://www.ncbi.nlm.nih.gov/pubmed/24079728
http://dx.doi.org/10.1186/1471-2148-13-217
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author Grayson, Phil
Civetta, Alberto
author_facet Grayson, Phil
Civetta, Alberto
author_sort Grayson, Phil
collection PubMed
description BACKGROUND: Sperm and testes-expressed Adam genes have been shown to undergo bouts of positive selection in mammals. Despite the pervasiveness of positive selection signals, it is unclear what has driven such selective bouts. The fact that only sperm surface Adam genes show signals of positive selection within their adhesion domain has led to speculation that selection might be driven by species-specific adaptations to fertilization or sperm competition. Alternatively, duplications and neofunctionalization of Adam sperm surface genes, particularly as it is now understood in rodents, might have contributed to an acceleration of evolutionary rates and possibly adaptive diversification. RESULTS: Here we sequenced and conducted tests of selection within the adhesion domain of sixteen known sperm-surface Adam genes among five species of the Mus genus. We find evidence of positive selection associated with all six Adam genes known to interact to form functional complexes on Mus sperm. A subset of these complex-forming sperm genes also displayed accelerated branch evolution with Adam5 evolving under positive selection. In contrast to our previous findings in primates, selective bouts within Mus sperm Adams showed no associations to proxies of sperm competition. Expanded phylogenetic analysis including sequence data from other placental mammals allowed us to uncover ancient and recent episodes of adaptive evolution. CONCLUSIONS: The prevailing signals of rapid divergence and positive selection detected within the adhesion domain of interacting sperm Adams is driven by duplications and potential neofunctionalizations that are in some cases ancient (Adams 2, 3 and 5) or more recent (Adams 1b, 4b and 6).
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spelling pubmed-38499672013-12-05 Positive selection in the adhesion domain of Mus sperm Adam genes through gene duplications and function-driven gene complex formations Grayson, Phil Civetta, Alberto BMC Evol Biol Research Article BACKGROUND: Sperm and testes-expressed Adam genes have been shown to undergo bouts of positive selection in mammals. Despite the pervasiveness of positive selection signals, it is unclear what has driven such selective bouts. The fact that only sperm surface Adam genes show signals of positive selection within their adhesion domain has led to speculation that selection might be driven by species-specific adaptations to fertilization or sperm competition. Alternatively, duplications and neofunctionalization of Adam sperm surface genes, particularly as it is now understood in rodents, might have contributed to an acceleration of evolutionary rates and possibly adaptive diversification. RESULTS: Here we sequenced and conducted tests of selection within the adhesion domain of sixteen known sperm-surface Adam genes among five species of the Mus genus. We find evidence of positive selection associated with all six Adam genes known to interact to form functional complexes on Mus sperm. A subset of these complex-forming sperm genes also displayed accelerated branch evolution with Adam5 evolving under positive selection. In contrast to our previous findings in primates, selective bouts within Mus sperm Adams showed no associations to proxies of sperm competition. Expanded phylogenetic analysis including sequence data from other placental mammals allowed us to uncover ancient and recent episodes of adaptive evolution. CONCLUSIONS: The prevailing signals of rapid divergence and positive selection detected within the adhesion domain of interacting sperm Adams is driven by duplications and potential neofunctionalizations that are in some cases ancient (Adams 2, 3 and 5) or more recent (Adams 1b, 4b and 6). BioMed Central 2013-09-30 /pmc/articles/PMC3849967/ /pubmed/24079728 http://dx.doi.org/10.1186/1471-2148-13-217 Text en Copyright © 2013 Grayson and Civetta; 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
Grayson, Phil
Civetta, Alberto
Positive selection in the adhesion domain of Mus sperm Adam genes through gene duplications and function-driven gene complex formations
title Positive selection in the adhesion domain of Mus sperm Adam genes through gene duplications and function-driven gene complex formations
title_full Positive selection in the adhesion domain of Mus sperm Adam genes through gene duplications and function-driven gene complex formations
title_fullStr Positive selection in the adhesion domain of Mus sperm Adam genes through gene duplications and function-driven gene complex formations
title_full_unstemmed Positive selection in the adhesion domain of Mus sperm Adam genes through gene duplications and function-driven gene complex formations
title_short Positive selection in the adhesion domain of Mus sperm Adam genes through gene duplications and function-driven gene complex formations
title_sort positive selection in the adhesion domain of mus sperm adam genes through gene duplications and function-driven gene complex formations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3849967/
https://www.ncbi.nlm.nih.gov/pubmed/24079728
http://dx.doi.org/10.1186/1471-2148-13-217
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