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Mating systems and protein–protein interactions determine evolutionary rates of primate sperm proteins

To assess the relative impact of functional constraint and post-mating sexual selection on sequence evolution of reproductive proteins, we examined 169 primate sperm proteins. In order to recognize potential genome-wide trends, we additionally analysed a sample of altogether 318 non-reproductive (br...

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Detalles Bibliográficos
Autores principales: Schumacher, Julia, Rosenkranz, David, Herlyn, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866406/
https://www.ncbi.nlm.nih.gov/pubmed/24307672
http://dx.doi.org/10.1098/rspb.2013.2607
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author Schumacher, Julia
Rosenkranz, David
Herlyn, Holger
author_facet Schumacher, Julia
Rosenkranz, David
Herlyn, Holger
author_sort Schumacher, Julia
collection PubMed
description To assess the relative impact of functional constraint and post-mating sexual selection on sequence evolution of reproductive proteins, we examined 169 primate sperm proteins. In order to recognize potential genome-wide trends, we additionally analysed a sample of altogether 318 non-reproductive (brain and postsynaptic) proteins. Based on cDNAs of eight primate species (Anthropoidea), we observed that pre-mating sperm proteins engaged in sperm composition and assembly show significantly lower incidence of site-specific positive selection and overall lower non-synonymous to synonymous substitution rates (d(N)/d(S)) across sites as compared with post-mating sperm proteins involved in capacitation, hyperactivation, acrosome reaction and fertilization. Moreover, database screening revealed overall more intracellular protein interaction partners in pre-mating than in post-mating sperm proteins. Finally, post-mating sperm proteins evolved at significantly higher evolutionary rates than pre-mating sperm and non-reproductive proteins on the branches to multi-male breeding species, while no such increase was observed on the branches to unimale and monogamous species. We conclude that less protein–protein interactions of post-mating sperm proteins account for lowered functional constraint, allowing for stronger impact of post-mating sexual selection, while the opposite holds true for pre-mating sperm proteins. This pattern is particularly strong in multi-male breeding species showing high female promiscuity.
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spelling pubmed-38664062014-01-22 Mating systems and protein–protein interactions determine evolutionary rates of primate sperm proteins Schumacher, Julia Rosenkranz, David Herlyn, Holger Proc Biol Sci Research Articles To assess the relative impact of functional constraint and post-mating sexual selection on sequence evolution of reproductive proteins, we examined 169 primate sperm proteins. In order to recognize potential genome-wide trends, we additionally analysed a sample of altogether 318 non-reproductive (brain and postsynaptic) proteins. Based on cDNAs of eight primate species (Anthropoidea), we observed that pre-mating sperm proteins engaged in sperm composition and assembly show significantly lower incidence of site-specific positive selection and overall lower non-synonymous to synonymous substitution rates (d(N)/d(S)) across sites as compared with post-mating sperm proteins involved in capacitation, hyperactivation, acrosome reaction and fertilization. Moreover, database screening revealed overall more intracellular protein interaction partners in pre-mating than in post-mating sperm proteins. Finally, post-mating sperm proteins evolved at significantly higher evolutionary rates than pre-mating sperm and non-reproductive proteins on the branches to multi-male breeding species, while no such increase was observed on the branches to unimale and monogamous species. We conclude that less protein–protein interactions of post-mating sperm proteins account for lowered functional constraint, allowing for stronger impact of post-mating sexual selection, while the opposite holds true for pre-mating sperm proteins. This pattern is particularly strong in multi-male breeding species showing high female promiscuity. The Royal Society 2014-01-22 /pmc/articles/PMC3866406/ /pubmed/24307672 http://dx.doi.org/10.1098/rspb.2013.2607 Text en http://creativecommons.org/licenses/by/3.0/ © 2013 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research Articles
Schumacher, Julia
Rosenkranz, David
Herlyn, Holger
Mating systems and protein–protein interactions determine evolutionary rates of primate sperm proteins
title Mating systems and protein–protein interactions determine evolutionary rates of primate sperm proteins
title_full Mating systems and protein–protein interactions determine evolutionary rates of primate sperm proteins
title_fullStr Mating systems and protein–protein interactions determine evolutionary rates of primate sperm proteins
title_full_unstemmed Mating systems and protein–protein interactions determine evolutionary rates of primate sperm proteins
title_short Mating systems and protein–protein interactions determine evolutionary rates of primate sperm proteins
title_sort mating systems and protein–protein interactions determine evolutionary rates of primate sperm proteins
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866406/
https://www.ncbi.nlm.nih.gov/pubmed/24307672
http://dx.doi.org/10.1098/rspb.2013.2607
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