Meiosis reveals the early steps in the evolution of a neo-XY sex chromosome pair in the African pygmy mouse Mus minutoides

Author summary Sex chromosomes seem to evolve and differentiate at different rates in different taxa. The reasons for this variability are still debated. It is well established that recombination suppression around the sex-determining region triggers differentiation, and several studies have investi...

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Veröffentlicht in:PLoS genetics 2020-11, Vol.16 (11), p.e1008959, Article 1008959
Hauptverfasser: Gil-Fernandez, Ana, Saunders, Paul A., Martin-Ruiz, Marta, Ribagorda, Marta, Lopez-Jimenez, Pablo, Jeffries, Daniel L., Parra, Maria Teresa, Viera, Alberto, Rufas, Julio S., Perrin, Nicolas, Veyrunes, Frederic, Page, Jesus
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container_issue 11
container_start_page e1008959
container_title PLoS genetics
container_volume 16
creator Gil-Fernandez, Ana
Saunders, Paul A.
Martin-Ruiz, Marta
Ribagorda, Marta
Lopez-Jimenez, Pablo
Jeffries, Daniel L.
Parra, Maria Teresa
Viera, Alberto
Rufas, Julio S.
Perrin, Nicolas
Veyrunes, Frederic
Page, Jesus
description Author summary Sex chromosomes seem to evolve and differentiate at different rates in different taxa. The reasons for this variability are still debated. It is well established that recombination suppression around the sex-determining region triggers differentiation, and several studies have investigated this process from a genetic point of view. However, the cellular context in which recombination arrest occurs has received little attention so far. In this report, we show that meiosis, the cellular division in which pairing and recombination between chromosomes takes place, can affect the incipient differentiation of X and Y chromosomes. Combining cytogenetic and genomic approaches, we found that in the African pygmy mouse Mus minutoides, which has recently undergone sex chromosome-autosome fusions, synapsis and DNA repair dynamics are disturbed along the newly added region of the sex chromosomes. We argue that these alterations are a by-product of the fusion itself, and cause recombination suppression across a large region of the neo-sex chromosome pair. Therefore, we propose that the meiotic context in which sex or neo-sex chromosomes arise is crucial to understand the very early stages of their differentiation, as it could promote or hinder recombination suppression, and therefore impact the rate at which these chromosomes differentiate. Sex chromosomes of eutherian mammals are highly different in size and gene content, and share only a small region of homology (pseudoautosomal region, PAR). They are thought to have evolved through an addition-attrition cycle involving the addition of autosomal segments to sex chromosomes and their subsequent differentiation. The events that drive this process are difficult to investigate because sex chromosomes in almost all mammals are at a very advanced stage of differentiation. Here, we have taken advantage of a recent translocation of an autosome to both sex chromosomes in the African pygmy mouse Mus minutoides, which has restored a large segment of homology (neo-PAR). By studying meiotic sex chromosome behavior and identifying fully sex-linked genetic markers in the neo-PAR, we demonstrate that this region shows unequivocal signs of early sex-differentiation. First, synapsis and resolution of DNA damage intermediates are delayed in the neo-PAR during meiosis. Second, recombination is suppressed or largely reduced in a large portion of the neo-PAR. However, the inactivation process that characterizes sex chromosom
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The reasons for this variability are still debated. It is well established that recombination suppression around the sex-determining region triggers differentiation, and several studies have investigated this process from a genetic point of view. However, the cellular context in which recombination arrest occurs has received little attention so far. In this report, we show that meiosis, the cellular division in which pairing and recombination between chromosomes takes place, can affect the incipient differentiation of X and Y chromosomes. Combining cytogenetic and genomic approaches, we found that in the African pygmy mouse Mus minutoides, which has recently undergone sex chromosome-autosome fusions, synapsis and DNA repair dynamics are disturbed along the newly added region of the sex chromosomes. We argue that these alterations are a by-product of the fusion itself, and cause recombination suppression across a large region of the neo-sex chromosome pair. Therefore, we propose that the meiotic context in which sex or neo-sex chromosomes arise is crucial to understand the very early stages of their differentiation, as it could promote or hinder recombination suppression, and therefore impact the rate at which these chromosomes differentiate. Sex chromosomes of eutherian mammals are highly different in size and gene content, and share only a small region of homology (pseudoautosomal region, PAR). They are thought to have evolved through an addition-attrition cycle involving the addition of autosomal segments to sex chromosomes and their subsequent differentiation. The events that drive this process are difficult to investigate because sex chromosomes in almost all mammals are at a very advanced stage of differentiation. Here, we have taken advantage of a recent translocation of an autosome to both sex chromosomes in the African pygmy mouse Mus minutoides, which has restored a large segment of homology (neo-PAR). By studying meiotic sex chromosome behavior and identifying fully sex-linked genetic markers in the neo-PAR, we demonstrate that this region shows unequivocal signs of early sex-differentiation. First, synapsis and resolution of DNA damage intermediates are delayed in the neo-PAR during meiosis. Second, recombination is suppressed or largely reduced in a large portion of the neo-PAR. However, the inactivation process that characterizes sex chromosomes during meiosis does not extend to this region. Finally, the sex chromosomes show a dual mechanism of association at metaphase-I that involves the formation of a chiasma in the neo-PAR and the preservation of an ancestral achiasmate mode of association in the non-homologous segments. We show that the study of meiosis is crucial to apprehend the onset of sex chromosome differentiation, as it introduces structural and functional constrains to sex chromosome evolution. Synapsis and DNA repair dynamics are the first processes affected in the incipient differentiation of X and Y chromosomes, and they may be involved in accelerating their evolution. This provides one of the very first reports of early steps in neo-sex chromosome differentiation in mammals, and for the first time a cellular framework for the addition-attrition model of sex chromosome evolution.</description><identifier>ISSN: 1553-7404</identifier><identifier>ISSN: 1553-7390</identifier><identifier>EISSN: 1553-7404</identifier><identifier>DOI: 10.1371/journal.pgen.1008959</identifier><identifier>PMID: 33180767</identifier><language>eng</language><publisher>SAN FRANCISCO: Public Library Science</publisher><subject>Animal behavior ; Animals ; Biology and Life Sciences ; Cell division ; Chiasma ; Deoxyribonucleic acid ; Divergence ; DNA ; DNA repair ; Epigenetics ; Eutheria - genetics ; Evolution ; Female ; Genetic aspects ; Genetics &amp; Heredity ; Homology ; Life Sciences ; Life Sciences &amp; Biomedicine ; Male ; Mammals ; Mammals - genetics ; Meiosis ; Meiosis - genetics ; Metaphase ; Mice - genetics ; Murinae ; Natural history ; Pseudoautosomal Regions ; Recombination ; Research and Analysis Methods ; Science &amp; Technology ; Sex chromosomes ; Sex Chromosomes - genetics ; Sex Differentiation - genetics ; Transcription ; Translocation, Genetic - genetics ; X Chromosome - genetics ; Y Chromosome - genetics ; Y chromosomes</subject><ispartof>PLoS genetics, 2020-11, Vol.16 (11), p.e1008959, Article 1008959</ispartof><rights>COPYRIGHT 2020 Public Library of Science</rights><rights>2020 Gil-Fernández 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, and reproduction in any medium, provided the original author and source are credited. 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>2020 Gil-Fernández et al 2020 Gil-Fernández et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>11</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000593890600001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c760t-c4393d16ee9973c79ff15b239d22d99950b5361d1aa0d994a11da71337303e553</citedby><cites>FETCH-LOGICAL-c760t-c4393d16ee9973c79ff15b239d22d99950b5361d1aa0d994a11da71337303e553</cites><orcidid>0000-0002-7516-809X ; 0000-0002-7756-6323 ; 0000-0002-1706-9915 ; 0000-0002-3602-4130 ; 0000-0001-9394-5625 ; 0000-0003-0711-8979 ; 0000-0002-9707-1635 ; 0000-0002-1158-6903 ; 0000-0003-1701-3978 ; 0000-0002-6673-5996 ; 0000-0002-6282-0472 ; 0000-0001-8381-324X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685469/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685469/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,866,887,2106,2118,2932,23875,27933,27934,28257,53800,53802</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33180767$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03043639$$DView record in HAL$$Hfree_for_read</backlink></links><search><contributor>Keeney, Scott</contributor><creatorcontrib>Gil-Fernandez, Ana</creatorcontrib><creatorcontrib>Saunders, Paul A.</creatorcontrib><creatorcontrib>Martin-Ruiz, Marta</creatorcontrib><creatorcontrib>Ribagorda, Marta</creatorcontrib><creatorcontrib>Lopez-Jimenez, Pablo</creatorcontrib><creatorcontrib>Jeffries, Daniel L.</creatorcontrib><creatorcontrib>Parra, Maria Teresa</creatorcontrib><creatorcontrib>Viera, Alberto</creatorcontrib><creatorcontrib>Rufas, Julio S.</creatorcontrib><creatorcontrib>Perrin, Nicolas</creatorcontrib><creatorcontrib>Veyrunes, Frederic</creatorcontrib><creatorcontrib>Page, Jesus</creatorcontrib><title>Meiosis reveals the early steps in the evolution of a neo-XY sex chromosome pair in the African pygmy mouse Mus minutoides</title><title>PLoS genetics</title><addtitle>PLOS GENET</addtitle><addtitle>PLoS Genet</addtitle><description>Author summary Sex chromosomes seem to evolve and differentiate at different rates in different taxa. The reasons for this variability are still debated. It is well established that recombination suppression around the sex-determining region triggers differentiation, and several studies have investigated this process from a genetic point of view. However, the cellular context in which recombination arrest occurs has received little attention so far. In this report, we show that meiosis, the cellular division in which pairing and recombination between chromosomes takes place, can affect the incipient differentiation of X and Y chromosomes. Combining cytogenetic and genomic approaches, we found that in the African pygmy mouse Mus minutoides, which has recently undergone sex chromosome-autosome fusions, synapsis and DNA repair dynamics are disturbed along the newly added region of the sex chromosomes. We argue that these alterations are a by-product of the fusion itself, and cause recombination suppression across a large region of the neo-sex chromosome pair. Therefore, we propose that the meiotic context in which sex or neo-sex chromosomes arise is crucial to understand the very early stages of their differentiation, as it could promote or hinder recombination suppression, and therefore impact the rate at which these chromosomes differentiate. Sex chromosomes of eutherian mammals are highly different in size and gene content, and share only a small region of homology (pseudoautosomal region, PAR). They are thought to have evolved through an addition-attrition cycle involving the addition of autosomal segments to sex chromosomes and their subsequent differentiation. The events that drive this process are difficult to investigate because sex chromosomes in almost all mammals are at a very advanced stage of differentiation. Here, we have taken advantage of a recent translocation of an autosome to both sex chromosomes in the African pygmy mouse Mus minutoides, which has restored a large segment of homology (neo-PAR). By studying meiotic sex chromosome behavior and identifying fully sex-linked genetic markers in the neo-PAR, we demonstrate that this region shows unequivocal signs of early sex-differentiation. First, synapsis and resolution of DNA damage intermediates are delayed in the neo-PAR during meiosis. Second, recombination is suppressed or largely reduced in a large portion of the neo-PAR. However, the inactivation process that characterizes sex chromosomes during meiosis does not extend to this region. Finally, the sex chromosomes show a dual mechanism of association at metaphase-I that involves the formation of a chiasma in the neo-PAR and the preservation of an ancestral achiasmate mode of association in the non-homologous segments. We show that the study of meiosis is crucial to apprehend the onset of sex chromosome differentiation, as it introduces structural and functional constrains to sex chromosome evolution. Synapsis and DNA repair dynamics are the first processes affected in the incipient differentiation of X and Y chromosomes, and they may be involved in accelerating their evolution. This provides one of the very first reports of early steps in neo-sex chromosome differentiation in mammals, and for the first time a cellular framework for the addition-attrition model of sex chromosome evolution.</description><subject>Animal behavior</subject><subject>Animals</subject><subject>Biology and Life Sciences</subject><subject>Cell division</subject><subject>Chiasma</subject><subject>Deoxyribonucleic acid</subject><subject>Divergence</subject><subject>DNA</subject><subject>DNA repair</subject><subject>Epigenetics</subject><subject>Eutheria - genetics</subject><subject>Evolution</subject><subject>Female</subject><subject>Genetic aspects</subject><subject>Genetics &amp; Heredity</subject><subject>Homology</subject><subject>Life Sciences</subject><subject>Life Sciences &amp; Biomedicine</subject><subject>Male</subject><subject>Mammals</subject><subject>Mammals - genetics</subject><subject>Meiosis</subject><subject>Meiosis - genetics</subject><subject>Metaphase</subject><subject>Mice - genetics</subject><subject>Murinae</subject><subject>Natural history</subject><subject>Pseudoautosomal Regions</subject><subject>Recombination</subject><subject>Research and Analysis Methods</subject><subject>Science &amp; 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Technology</topic><topic>Sex chromosomes</topic><topic>Sex Chromosomes - genetics</topic><topic>Sex Differentiation - genetics</topic><topic>Transcription</topic><topic>Translocation, Genetic - genetics</topic><topic>X Chromosome - genetics</topic><topic>Y Chromosome - genetics</topic><topic>Y chromosomes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gil-Fernandez, Ana</creatorcontrib><creatorcontrib>Saunders, Paul A.</creatorcontrib><creatorcontrib>Martin-Ruiz, Marta</creatorcontrib><creatorcontrib>Ribagorda, Marta</creatorcontrib><creatorcontrib>Lopez-Jimenez, Pablo</creatorcontrib><creatorcontrib>Jeffries, Daniel L.</creatorcontrib><creatorcontrib>Parra, Maria Teresa</creatorcontrib><creatorcontrib>Viera, Alberto</creatorcontrib><creatorcontrib>Rufas, Julio S.</creatorcontrib><creatorcontrib>Perrin, Nicolas</creatorcontrib><creatorcontrib>Veyrunes, Frederic</creatorcontrib><creatorcontrib>Page, Jesus</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; 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Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Access via ProQuest (Open Access)</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>Genetics Abstracts</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gil-Fernandez, Ana</au><au>Saunders, Paul A.</au><au>Martin-Ruiz, Marta</au><au>Ribagorda, Marta</au><au>Lopez-Jimenez, Pablo</au><au>Jeffries, Daniel L.</au><au>Parra, Maria Teresa</au><au>Viera, Alberto</au><au>Rufas, Julio S.</au><au>Perrin, Nicolas</au><au>Veyrunes, Frederic</au><au>Page, Jesus</au><au>Keeney, Scott</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Meiosis reveals the early steps in the evolution of a neo-XY sex chromosome pair in the African pygmy mouse Mus minutoides</atitle><jtitle>PLoS genetics</jtitle><stitle>PLOS GENET</stitle><addtitle>PLoS Genet</addtitle><date>2020-11-12</date><risdate>2020</risdate><volume>16</volume><issue>11</issue><spage>e1008959</spage><pages>e1008959-</pages><artnum>1008959</artnum><issn>1553-7404</issn><issn>1553-7390</issn><eissn>1553-7404</eissn><abstract>Author summary Sex chromosomes seem to evolve and differentiate at different rates in different taxa. The reasons for this variability are still debated. It is well established that recombination suppression around the sex-determining region triggers differentiation, and several studies have investigated this process from a genetic point of view. However, the cellular context in which recombination arrest occurs has received little attention so far. In this report, we show that meiosis, the cellular division in which pairing and recombination between chromosomes takes place, can affect the incipient differentiation of X and Y chromosomes. Combining cytogenetic and genomic approaches, we found that in the African pygmy mouse Mus minutoides, which has recently undergone sex chromosome-autosome fusions, synapsis and DNA repair dynamics are disturbed along the newly added region of the sex chromosomes. We argue that these alterations are a by-product of the fusion itself, and cause recombination suppression across a large region of the neo-sex chromosome pair. Therefore, we propose that the meiotic context in which sex or neo-sex chromosomes arise is crucial to understand the very early stages of their differentiation, as it could promote or hinder recombination suppression, and therefore impact the rate at which these chromosomes differentiate. Sex chromosomes of eutherian mammals are highly different in size and gene content, and share only a small region of homology (pseudoautosomal region, PAR). They are thought to have evolved through an addition-attrition cycle involving the addition of autosomal segments to sex chromosomes and their subsequent differentiation. The events that drive this process are difficult to investigate because sex chromosomes in almost all mammals are at a very advanced stage of differentiation. Here, we have taken advantage of a recent translocation of an autosome to both sex chromosomes in the African pygmy mouse Mus minutoides, which has restored a large segment of homology (neo-PAR). By studying meiotic sex chromosome behavior and identifying fully sex-linked genetic markers in the neo-PAR, we demonstrate that this region shows unequivocal signs of early sex-differentiation. First, synapsis and resolution of DNA damage intermediates are delayed in the neo-PAR during meiosis. Second, recombination is suppressed or largely reduced in a large portion of the neo-PAR. However, the inactivation process that characterizes sex chromosomes during meiosis does not extend to this region. Finally, the sex chromosomes show a dual mechanism of association at metaphase-I that involves the formation of a chiasma in the neo-PAR and the preservation of an ancestral achiasmate mode of association in the non-homologous segments. We show that the study of meiosis is crucial to apprehend the onset of sex chromosome differentiation, as it introduces structural and functional constrains to sex chromosome evolution. Synapsis and DNA repair dynamics are the first processes affected in the incipient differentiation of X and Y chromosomes, and they may be involved in accelerating their evolution. This provides one of the very first reports of early steps in neo-sex chromosome differentiation in mammals, and for the first time a cellular framework for the addition-attrition model of sex chromosome evolution.</abstract><cop>SAN FRANCISCO</cop><pub>Public Library Science</pub><pmid>33180767</pmid><doi>10.1371/journal.pgen.1008959</doi><tpages>27</tpages><orcidid>https://orcid.org/0000-0002-7516-809X</orcidid><orcidid>https://orcid.org/0000-0002-7756-6323</orcidid><orcidid>https://orcid.org/0000-0002-1706-9915</orcidid><orcidid>https://orcid.org/0000-0002-3602-4130</orcidid><orcidid>https://orcid.org/0000-0001-9394-5625</orcidid><orcidid>https://orcid.org/0000-0003-0711-8979</orcidid><orcidid>https://orcid.org/0000-0002-9707-1635</orcidid><orcidid>https://orcid.org/0000-0002-1158-6903</orcidid><orcidid>https://orcid.org/0000-0003-1701-3978</orcidid><orcidid>https://orcid.org/0000-0002-6673-5996</orcidid><orcidid>https://orcid.org/0000-0002-6282-0472</orcidid><orcidid>https://orcid.org/0000-0001-8381-324X</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1553-7404
ispartof PLoS genetics, 2020-11, Vol.16 (11), p.e1008959, Article 1008959
issn 1553-7404
1553-7390
1553-7404
language eng
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source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS) Journals Open Access; Web of Science - Science Citation Index Expanded - 2020<img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" />; PubMed Central
subjects Animal behavior
Animals
Biology and Life Sciences
Cell division
Chiasma
Deoxyribonucleic acid
Divergence
DNA
DNA repair
Epigenetics
Eutheria - genetics
Evolution
Female
Genetic aspects
Genetics & Heredity
Homology
Life Sciences
Life Sciences & Biomedicine
Male
Mammals
Mammals - genetics
Meiosis
Meiosis - genetics
Metaphase
Mice - genetics
Murinae
Natural history
Pseudoautosomal Regions
Recombination
Research and Analysis Methods
Science & Technology
Sex chromosomes
Sex Chromosomes - genetics
Sex Differentiation - genetics
Transcription
Translocation, Genetic - genetics
X Chromosome - genetics
Y Chromosome - genetics
Y chromosomes
title Meiosis reveals the early steps in the evolution of a neo-XY sex chromosome pair in the African pygmy mouse Mus minutoides
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