Mouse EWSR1 is crucial for spermatid post-meiotic transcription and spermiogenesis
Spermatogenesis is precisely controlled by complex gene-expression programs. During mammalian male germ-cell development, a crucial feature is the repression of transcription before spermatid elongation. Previously, we discovered that the RNA-binding protein EWSR1 plays an important role in meiotic...
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Veröffentlicht in: | Development (Cambridge) 2021-06, Vol.148 (11) |
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description | Spermatogenesis is precisely controlled by complex gene-expression programs. During mammalian male germ-cell development, a crucial feature is the repression of transcription before spermatid elongation. Previously, we discovered that the RNA-binding protein EWSR1 plays an important role in meiotic recombination in mouse, and showed that EWSR1 is highly expressed in late meiotic cells and post-meiotic cells. Here, we used an Ewsr1 pachytene stage-specific knockout mouse model to study the roles of Ewsr1 in late meiotic prophase I and in spermatozoa maturation. We show that loss of EWSR1 in late meiotic prophase I does not affect proper meiosis completion, but does result in defective spermatid elongation and chromocenter formation in the developing germ cells. As a result, male mice lacking EWSR1 after pachynema are sterile. We found that, in Ewsr1 CKO round spermatids, transition from a meiotic gene-expression program to a post-meiotic and spermatid gene expression program related to DNA condensation is impaired, suggesting that EWSR1 plays an important role in regulation of spermiogenesis-related mRNA synthesis necessary for spermatid differentiation into mature sperm. |
doi_str_mv | 10.1242/dev.199414 |
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During mammalian male germ-cell development, a crucial feature is the repression of transcription before spermatid elongation. Previously, we discovered that the RNA-binding protein EWSR1 plays an important role in meiotic recombination in mouse, and showed that EWSR1 is highly expressed in late meiotic cells and post-meiotic cells. Here, we used an Ewsr1 pachytene stage-specific knockout mouse model to study the roles of Ewsr1 in late meiotic prophase I and in spermatozoa maturation. We show that loss of EWSR1 in late meiotic prophase I does not affect proper meiosis completion, but does result in defective spermatid elongation and chromocenter formation in the developing germ cells. As a result, male mice lacking EWSR1 after pachynema are sterile. We found that, in Ewsr1 CKO round spermatids, transition from a meiotic gene-expression program to a post-meiotic and spermatid gene expression program related to DNA condensation is impaired, suggesting that EWSR1 plays an important role in regulation of spermiogenesis-related mRNA synthesis necessary for spermatid differentiation into mature sperm.</description><identifier>ISSN: 0950-1991</identifier><identifier>EISSN: 1477-9129</identifier><identifier>DOI: 10.1242/dev.199414</identifier><identifier>PMID: 34100066</identifier><language>eng</language><publisher>The Company of Biologists Ltd</publisher><subject>Reproductive Biology</subject><ispartof>Development (Cambridge), 2021-06, Vol.148 (11)</ispartof><rights>2021. 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During mammalian male germ-cell development, a crucial feature is the repression of transcription before spermatid elongation. Previously, we discovered that the RNA-binding protein EWSR1 plays an important role in meiotic recombination in mouse, and showed that EWSR1 is highly expressed in late meiotic cells and post-meiotic cells. Here, we used an Ewsr1 pachytene stage-specific knockout mouse model to study the roles of Ewsr1 in late meiotic prophase I and in spermatozoa maturation. We show that loss of EWSR1 in late meiotic prophase I does not affect proper meiosis completion, but does result in defective spermatid elongation and chromocenter formation in the developing germ cells. As a result, male mice lacking EWSR1 after pachynema are sterile. We found that, in Ewsr1 CKO round spermatids, transition from a meiotic gene-expression program to a post-meiotic and spermatid gene expression program related to DNA condensation is impaired, suggesting that EWSR1 plays an important role in regulation of spermiogenesis-related mRNA synthesis necessary for spermatid differentiation into mature sperm.</description><subject>Reproductive Biology</subject><issn>0950-1991</issn><issn>1477-9129</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpVkU9LxDAQxYMo7rp68RP0KEI1adKmuQiyrH9gRVgVjyFNJmukbWrSLvjtrXQRPA3D-_HmMQ-hc4KvSMayawO7KyIEI-wAzQnjPBUkE4dojkWO01EhM3QS4yfGmBacH6MZZWRcimKONk9-iJCs3l82JHEx0WHQTtWJ9SGJHYRG9c4knY992oDzvdNJH1QbdXBd73ybqNZMoPNbaCG6eIqOrKojnO3nAr3drV6XD-n6-f5xebtONc3zPgVtGc000eWYqjJYCeAkx5yUipGqJJQXxholeGUKg3nOwTDLMPCSWgsU6ALdTL7dUDVgNLRjslp2wTUqfEuvnPyvtO5Dbv1OlhnhHBejwcXeIPivAWIvGxc11LVqYfyKzHIqMpzzshzRywnVwccYwP6dIVj-liDHEuRUAv0B9bh60Q</recordid><startdate>20210601</startdate><enddate>20210601</enddate><creator>Tian, Hui</creator><creator>Petkov, Petko M.</creator><general>The Company of Biologists Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6694-9150</orcidid></search><sort><creationdate>20210601</creationdate><title>Mouse EWSR1 is crucial for spermatid post-meiotic transcription and spermiogenesis</title><author>Tian, Hui ; Petkov, Petko M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c355t-ecf432c1c8036bd0a9e7150718a41b81376dfda97bd6d0757ed4f40e783ffe3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Reproductive Biology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tian, Hui</creatorcontrib><creatorcontrib>Petkov, Petko M.</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Development (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tian, Hui</au><au>Petkov, Petko M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mouse EWSR1 is crucial for spermatid post-meiotic transcription and spermiogenesis</atitle><jtitle>Development (Cambridge)</jtitle><date>2021-06-01</date><risdate>2021</risdate><volume>148</volume><issue>11</issue><issn>0950-1991</issn><eissn>1477-9129</eissn><abstract>Spermatogenesis is precisely controlled by complex gene-expression programs. During mammalian male germ-cell development, a crucial feature is the repression of transcription before spermatid elongation. Previously, we discovered that the RNA-binding protein EWSR1 plays an important role in meiotic recombination in mouse, and showed that EWSR1 is highly expressed in late meiotic cells and post-meiotic cells. Here, we used an Ewsr1 pachytene stage-specific knockout mouse model to study the roles of Ewsr1 in late meiotic prophase I and in spermatozoa maturation. We show that loss of EWSR1 in late meiotic prophase I does not affect proper meiosis completion, but does result in defective spermatid elongation and chromocenter formation in the developing germ cells. As a result, male mice lacking EWSR1 after pachynema are sterile. We found that, in Ewsr1 CKO round spermatids, transition from a meiotic gene-expression program to a post-meiotic and spermatid gene expression program related to DNA condensation is impaired, suggesting that EWSR1 plays an important role in regulation of spermiogenesis-related mRNA synthesis necessary for spermatid differentiation into mature sperm.</abstract><pub>The Company of Biologists Ltd</pub><pmid>34100066</pmid><doi>10.1242/dev.199414</doi><orcidid>https://orcid.org/0000-0002-6694-9150</orcidid><oa>free_for_read</oa></addata></record> |
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source | Company of Biologists,COB,生物学家联盟; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Reproductive Biology |
title | Mouse EWSR1 is crucial for spermatid post-meiotic transcription and spermiogenesis |
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