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Positive selection on human gamete-recognition genes
Coevolution of genes that encode interacting proteins expressed on the surfaces of sperm and eggs can lead to variation in reproductive compatibility between mates and reproductive isolation between members of different species. Previous studies in mice and other mammals have focused in particular o...
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Published in: | PeerJ (San Francisco, CA) CA), 2018-01, Vol.6, p.e4259-e4259, Article e4259 |
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description | Coevolution of genes that encode interacting proteins expressed on the surfaces of sperm and eggs can lead to variation in reproductive compatibility between mates and reproductive isolation between members of different species. Previous studies in mice and other mammals have focused in particular on evidence for positive or diversifying selection that shapes the evolution of genes that encode sperm-binding proteins expressed in the egg coat or zona pellucida (ZP). By fitting phylogenetic models of codon evolution to data from the 1000 Genomes Project, we identified candidate sites evolving under diversifying selection in the human genes
and
. We also identified one candidate site under positive selection in
, which encodes a repetitive protein similar to the mouse protein ZP3R that is expressed in the sperm head and binds to the ZP at fertilization. Results from several additional analyses that applied population genetic models to the same data were consistent with the hypothesis of selection on those candidate sites leading to coevolution of sperm- and egg-expressed genes. By contrast, we found no candidate sites under selection in a fourth gene (
) that encodes an egg coat structural protein not directly involved in sperm binding. Finally, we found that two of the candidate sites (in
and
) were correlated with variation in family size and birth rate among Hutterite couples, and those two candidate sites were also in linkage disequilibrium in the same Hutterite study population. All of these lines of evidence are consistent with predictions from a previously proposed hypothesis of balancing selection on epistatic interactions between
and
at fertilization that lead to the evolution of co-adapted allele pairs. Such patterns also suggest specific molecular traits that may be associated with both natural reproductive variation and clinical infertility. |
doi_str_mv | 10.7717/peerj.4259 |
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and
. We also identified one candidate site under positive selection in
, which encodes a repetitive protein similar to the mouse protein ZP3R that is expressed in the sperm head and binds to the ZP at fertilization. Results from several additional analyses that applied population genetic models to the same data were consistent with the hypothesis of selection on those candidate sites leading to coevolution of sperm- and egg-expressed genes. By contrast, we found no candidate sites under selection in a fourth gene (
) that encodes an egg coat structural protein not directly involved in sperm binding. Finally, we found that two of the candidate sites (in
and
) were correlated with variation in family size and birth rate among Hutterite couples, and those two candidate sites were also in linkage disequilibrium in the same Hutterite study population. All of these lines of evidence are consistent with predictions from a previously proposed hypothesis of balancing selection on epistatic interactions between
and
at fertilization that lead to the evolution of co-adapted allele pairs. Such patterns also suggest specific molecular traits that may be associated with both natural reproductive variation and clinical infertility.</description><identifier>ISSN: 2167-8359</identifier><identifier>EISSN: 2167-8359</identifier><identifier>DOI: 10.7717/peerj.4259</identifier><identifier>PMID: 29340252</identifier><language>eng</language><publisher>United States: PeerJ. Ltd</publisher><subject>Analysis ; Animal models ; Balancing selection ; Coevolution ; Consortia ; Developmental biology ; Eggs ; Epistasis ; Evolution ; Evolutionary genetics ; Evolutionary Studies ; Females ; Fertilization ; Genes ; Genetic aspects ; Genetics ; Genomes ; Germ cells ; Human reproduction ; Infertility ; Life Sciences ; Linkage disequilibrium ; Natural selection ; Phylogeny ; Population ; Population genetics ; Population studies ; Positive selection ; Proteins ; Reproductive isolation ; Sperm ; Studies ; Zona pellucida</subject><ispartof>PeerJ (San Francisco, CA), 2018-01, Vol.6, p.e4259-e4259, Article e4259</ispartof><rights>COPYRIGHT 2018 PeerJ. Ltd.</rights><rights>2018 Hart et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2018 Hart et al. 2018 Hart et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c641t-324836fd32aacdff020d6a2983cb73138c3c4a4a56add30d990ce406cbd8ddcf3</citedby><cites>FETCH-LOGICAL-c641t-324836fd32aacdff020d6a2983cb73138c3c4a4a56add30d990ce406cbd8ddcf3</cites><orcidid>0000-0003-4220-4928</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1986577234/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1986577234?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53770,53772,74873</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29340252$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04256661$$DView record in HAL$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-338674$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Hart, Michael W</creatorcontrib><creatorcontrib>Stover, Daryn A</creatorcontrib><creatorcontrib>Guerra, Vanessa</creatorcontrib><creatorcontrib>Mozaffari, Sahar V</creatorcontrib><creatorcontrib>Ober, Carole</creatorcontrib><creatorcontrib>Mugal, Carina F</creatorcontrib><creatorcontrib>Kaj, Ingemar</creatorcontrib><title>Positive selection on human gamete-recognition genes</title><title>PeerJ (San Francisco, CA)</title><addtitle>PeerJ</addtitle><description>Coevolution of genes that encode interacting proteins expressed on the surfaces of sperm and eggs can lead to variation in reproductive compatibility between mates and reproductive isolation between members of different species. Previous studies in mice and other mammals have focused in particular on evidence for positive or diversifying selection that shapes the evolution of genes that encode sperm-binding proteins expressed in the egg coat or zona pellucida (ZP). By fitting phylogenetic models of codon evolution to data from the 1000 Genomes Project, we identified candidate sites evolving under diversifying selection in the human genes
and
. We also identified one candidate site under positive selection in
, which encodes a repetitive protein similar to the mouse protein ZP3R that is expressed in the sperm head and binds to the ZP at fertilization. Results from several additional analyses that applied population genetic models to the same data were consistent with the hypothesis of selection on those candidate sites leading to coevolution of sperm- and egg-expressed genes. By contrast, we found no candidate sites under selection in a fourth gene (
) that encodes an egg coat structural protein not directly involved in sperm binding. Finally, we found that two of the candidate sites (in
and
) were correlated with variation in family size and birth rate among Hutterite couples, and those two candidate sites were also in linkage disequilibrium in the same Hutterite study population. All of these lines of evidence are consistent with predictions from a previously proposed hypothesis of balancing selection on epistatic interactions between
and
at fertilization that lead to the evolution of co-adapted allele pairs. 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Stover, Daryn A ; Guerra, Vanessa ; Mozaffari, Sahar V ; Ober, Carole ; Mugal, Carina F ; Kaj, Ingemar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c641t-324836fd32aacdff020d6a2983cb73138c3c4a4a56add30d990ce406cbd8ddcf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Analysis</topic><topic>Animal models</topic><topic>Balancing selection</topic><topic>Coevolution</topic><topic>Consortia</topic><topic>Developmental biology</topic><topic>Eggs</topic><topic>Epistasis</topic><topic>Evolution</topic><topic>Evolutionary genetics</topic><topic>Evolutionary Studies</topic><topic>Females</topic><topic>Fertilization</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetics</topic><topic>Genomes</topic><topic>Germ cells</topic><topic>Human reproduction</topic><topic>Infertility</topic><topic>Life Sciences</topic><topic>Linkage disequilibrium</topic><topic>Natural selection</topic><topic>Phylogeny</topic><topic>Population</topic><topic>Population genetics</topic><topic>Population studies</topic><topic>Positive selection</topic><topic>Proteins</topic><topic>Reproductive isolation</topic><topic>Sperm</topic><topic>Studies</topic><topic>Zona pellucida</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hart, Michael W</creatorcontrib><creatorcontrib>Stover, Daryn A</creatorcontrib><creatorcontrib>Guerra, Vanessa</creatorcontrib><creatorcontrib>Mozaffari, Sahar V</creatorcontrib><creatorcontrib>Ober, Carole</creatorcontrib><creatorcontrib>Mugal, Carina F</creatorcontrib><creatorcontrib>Kaj, Ingemar</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SWEPUB Uppsala universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Uppsala universitet</collection><collection>SwePub Articles full text</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PeerJ (San Francisco, CA)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hart, Michael W</au><au>Stover, Daryn A</au><au>Guerra, Vanessa</au><au>Mozaffari, Sahar V</au><au>Ober, Carole</au><au>Mugal, Carina F</au><au>Kaj, Ingemar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Positive selection on human gamete-recognition genes</atitle><jtitle>PeerJ (San Francisco, CA)</jtitle><addtitle>PeerJ</addtitle><date>2018-01-11</date><risdate>2018</risdate><volume>6</volume><spage>e4259</spage><epage>e4259</epage><pages>e4259-e4259</pages><artnum>e4259</artnum><issn>2167-8359</issn><eissn>2167-8359</eissn><abstract>Coevolution of genes that encode interacting proteins expressed on the surfaces of sperm and eggs can lead to variation in reproductive compatibility between mates and reproductive isolation between members of different species. Previous studies in mice and other mammals have focused in particular on evidence for positive or diversifying selection that shapes the evolution of genes that encode sperm-binding proteins expressed in the egg coat or zona pellucida (ZP). By fitting phylogenetic models of codon evolution to data from the 1000 Genomes Project, we identified candidate sites evolving under diversifying selection in the human genes
and
. We also identified one candidate site under positive selection in
, which encodes a repetitive protein similar to the mouse protein ZP3R that is expressed in the sperm head and binds to the ZP at fertilization. Results from several additional analyses that applied population genetic models to the same data were consistent with the hypothesis of selection on those candidate sites leading to coevolution of sperm- and egg-expressed genes. By contrast, we found no candidate sites under selection in a fourth gene (
) that encodes an egg coat structural protein not directly involved in sperm binding. Finally, we found that two of the candidate sites (in
and
) were correlated with variation in family size and birth rate among Hutterite couples, and those two candidate sites were also in linkage disequilibrium in the same Hutterite study population. All of these lines of evidence are consistent with predictions from a previously proposed hypothesis of balancing selection on epistatic interactions between
and
at fertilization that lead to the evolution of co-adapted allele pairs. Such patterns also suggest specific molecular traits that may be associated with both natural reproductive variation and clinical infertility.</abstract><cop>United States</cop><pub>PeerJ. Ltd</pub><pmid>29340252</pmid><doi>10.7717/peerj.4259</doi><orcidid>https://orcid.org/0000-0003-4220-4928</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animal models Balancing selection Coevolution Consortia Developmental biology Eggs Epistasis Evolution Evolutionary genetics Evolutionary Studies Females Fertilization Genes Genetic aspects Genetics Genomes Germ cells Human reproduction Infertility Life Sciences Linkage disequilibrium Natural selection Phylogeny Population Population genetics Population studies Positive selection Proteins Reproductive isolation Sperm Studies Zona pellucida |
title | Positive selection on human gamete-recognition genes |
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