Spata22, a Novel Vertebrate-Specific Gene, Is Required for Meiotic Progress in Mouse Germ Cells
The N-ethyl-N-nitrosourea-induced repro42 mutation, identified by a forward genetics strategy, causes both male and female infertility, with no other apparent phenotypes. Positional cloning led to the discovery of a nonsense mutation in Spata22, a hitherto uncharacterized gene conserved among bony v...
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Veröffentlicht in: | Biology of reproduction 2012-02, Vol.86 (2), p.45-45 |
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description | The N-ethyl-N-nitrosourea-induced repro42 mutation, identified by a forward genetics strategy, causes both male and female infertility, with no other apparent phenotypes. Positional cloning led to the discovery of a nonsense mutation in Spata22, a hitherto uncharacterized gene conserved among bony vertebrates. Expression of both transcript and protein is restricted predominantly to germ cells of both sexes. Germ cells of repro42 mutant mice express Spata22 transcript, but not SPATA22 protein. Gametogenesis is profoundly affected by the mutation, and germ cells in repro42 mutant mice do not progress beyond early meiotic prophase, with subsequent germ cell loss in both males and females. The Spata22 gene is essential for one or more key events of early meiotic prophase, as homologous chromosomes of mutant germ cells do not achieve normal synapsis or repair meiotic DNA double-strand breaks. The repro42 mutation thus identifies a novel mammalian germ cell-specific gene required for meiotic progression. |
doi_str_mv | 10.1095/biolreprod.111.095752 |
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Positional cloning led to the discovery of a nonsense mutation in Spata22, a hitherto uncharacterized gene conserved among bony vertebrates. Expression of both transcript and protein is restricted predominantly to germ cells of both sexes. Germ cells of repro42 mutant mice express Spata22 transcript, but not SPATA22 protein. Gametogenesis is profoundly affected by the mutation, and germ cells in repro42 mutant mice do not progress beyond early meiotic prophase, with subsequent germ cell loss in both males and females. The Spata22 gene is essential for one or more key events of early meiotic prophase, as homologous chromosomes of mutant germ cells do not achieve normal synapsis or repair meiotic DNA double-strand breaks. The repro42 mutation thus identifies a novel mammalian germ cell-specific gene required for meiotic progression.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1095/biolreprod.111.095752</identifier><identifier>PMID: 22011390</identifier><identifier>CODEN: BIREBV</identifier><language>eng</language><publisher>Madison, WI: Society for the Study of Reproduction</publisher><subject>Amino Acid Sequence ; Animals ; Biological and medical sciences ; Cell Cycle Proteins - analysis ; Cell Cycle Proteins - genetics ; Cell Cycle Proteins - physiology ; Chromosomes ; Cloning ; Codon, Nonsense - genetics ; DNA damage ; DNA repair ; Double-strand break repair ; Female ; Fundamental and applied biological sciences. Psychology ; Gametogenesis ; Germ cells ; Infertility ; Infertility, Female - genetics ; Infertility, Female - physiopathology ; Infertility, Male - genetics ; Infertility, Male - physiopathology ; Male ; Meiosis ; Meiosis - physiology ; Mice ; Mice, Inbred C3H ; Mice, Inbred C57BL ; Mice, Mutant Strains ; Molecular Sequence Data ; Nonsense mutation ; Oocytes - physiology ; Oogenesis - genetics ; Oogenesis - physiology ; Phenotype ; Prophase ; Proteins - analysis ; Proteins - genetics ; Proteins - physiology ; Sex ; Spermatocytes - physiology ; Spermatogenesis - genetics ; Spermatogenesis - physiology ; Transcription ; Vertebrates: reproduction</subject><ispartof>Biology of reproduction, 2012-02, Vol.86 (2), p.45-45</ispartof><rights>2015 INIST-CNRS</rights><rights>2012 by the Society for the Study of Reproduction, Inc. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25791028$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22011390$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LA SALLE, Sophie</creatorcontrib><creatorcontrib>PALMER, Kristina</creatorcontrib><creatorcontrib>O'BRIEN, Marilyn</creatorcontrib><creatorcontrib>SCHIMENTI, John C</creatorcontrib><creatorcontrib>EPPIG, John</creatorcontrib><creatorcontrib>HANDEL, Mary Ann</creatorcontrib><title>Spata22, a Novel Vertebrate-Specific Gene, Is Required for Meiotic Progress in Mouse Germ Cells</title><title>Biology of reproduction</title><addtitle>Biol Reprod</addtitle><description>The N-ethyl-N-nitrosourea-induced repro42 mutation, identified by a forward genetics strategy, causes both male and female infertility, with no other apparent phenotypes. Positional cloning led to the discovery of a nonsense mutation in Spata22, a hitherto uncharacterized gene conserved among bony vertebrates. Expression of both transcript and protein is restricted predominantly to germ cells of both sexes. Germ cells of repro42 mutant mice express Spata22 transcript, but not SPATA22 protein. Gametogenesis is profoundly affected by the mutation, and germ cells in repro42 mutant mice do not progress beyond early meiotic prophase, with subsequent germ cell loss in both males and females. The Spata22 gene is essential for one or more key events of early meiotic prophase, as homologous chromosomes of mutant germ cells do not achieve normal synapsis or repair meiotic DNA double-strand breaks. The repro42 mutation thus identifies a novel mammalian germ cell-specific gene required for meiotic progression.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Cycle Proteins - analysis</subject><subject>Cell Cycle Proteins - genetics</subject><subject>Cell Cycle Proteins - physiology</subject><subject>Chromosomes</subject><subject>Cloning</subject><subject>Codon, Nonsense - genetics</subject><subject>DNA damage</subject><subject>DNA repair</subject><subject>Double-strand break repair</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gametogenesis</subject><subject>Germ cells</subject><subject>Infertility</subject><subject>Infertility, Female - genetics</subject><subject>Infertility, Female - physiopathology</subject><subject>Infertility, Male - genetics</subject><subject>Infertility, Male - physiopathology</subject><subject>Male</subject><subject>Meiosis</subject><subject>Meiosis - physiology</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Mutant Strains</subject><subject>Molecular Sequence Data</subject><subject>Nonsense mutation</subject><subject>Oocytes - physiology</subject><subject>Oogenesis - genetics</subject><subject>Oogenesis - physiology</subject><subject>Phenotype</subject><subject>Prophase</subject><subject>Proteins - analysis</subject><subject>Proteins - genetics</subject><subject>Proteins - physiology</subject><subject>Sex</subject><subject>Spermatocytes - physiology</subject><subject>Spermatogenesis - genetics</subject><subject>Spermatogenesis - physiology</subject><subject>Transcription</subject><subject>Vertebrates: reproduction</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFv1DAQhS0EokvhJ4B8QXBolhk7duxLJbSCUqkFRIFr5DiTYpSNUztbqf8eI7aFXjiN9N6np_eGsecIawSr3nQhjonmFPs1Iq6L1CjxgK1QCVs1QpuHbAUAupJSywP2JOefAFhLIR-zAyEAUVpYsfZidosT4og7_jFe08i_U1qoS26h6mImH4bg-QlNdMRPM_9CV7uQqOdDTPycQlyK-znFy0Q58zDx87jLVPi05Rsax_yUPRrcmOnZ_h6yb-_ffd18qM4-nZxu3p5VsxRmqbC2ILDRtVe9V9o13WCtVHVnzGBqqdBbBSBdX2QU2CMOpvOgegu9s8LIQ3b8J3fedVvqPU1LcmM7p7B16aaNLrT3nSn8aC_jdSuFBa1tCXi1D0jxakd5abch-zLBTVQ2tVZoVKAFFvL1f0kEYQBNDaKgL_5tdVfn9v8FeLkHXPZuHJKbfMh_OdXY33HyF6iVlbU</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>LA SALLE, Sophie</creator><creator>PALMER, Kristina</creator><creator>O'BRIEN, Marilyn</creator><creator>SCHIMENTI, John C</creator><creator>EPPIG, John</creator><creator>HANDEL, Mary Ann</creator><general>Society for the Study of Reproduction</general><general>Society for the Study of Reproduction, Inc</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120201</creationdate><title>Spata22, a Novel Vertebrate-Specific Gene, Is Required for Meiotic Progress in Mouse Germ Cells</title><author>LA SALLE, Sophie ; PALMER, Kristina ; O'BRIEN, Marilyn ; SCHIMENTI, John C ; EPPIG, John ; HANDEL, Mary Ann</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p328t-149021764c5dc56a7bf99354b88f84351c95003adf99121d11f8bc05d90da9283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Cycle Proteins - analysis</topic><topic>Cell Cycle Proteins - genetics</topic><topic>Cell Cycle Proteins - physiology</topic><topic>Chromosomes</topic><topic>Cloning</topic><topic>Codon, Nonsense - genetics</topic><topic>DNA damage</topic><topic>DNA repair</topic><topic>Double-strand break repair</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gametogenesis</topic><topic>Germ cells</topic><topic>Infertility</topic><topic>Infertility, Female - genetics</topic><topic>Infertility, Female - physiopathology</topic><topic>Infertility, Male - genetics</topic><topic>Infertility, Male - physiopathology</topic><topic>Male</topic><topic>Meiosis</topic><topic>Meiosis - physiology</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Mutant Strains</topic><topic>Molecular Sequence Data</topic><topic>Nonsense mutation</topic><topic>Oocytes - physiology</topic><topic>Oogenesis - genetics</topic><topic>Oogenesis - physiology</topic><topic>Phenotype</topic><topic>Prophase</topic><topic>Proteins - analysis</topic><topic>Proteins - genetics</topic><topic>Proteins - physiology</topic><topic>Sex</topic><topic>Spermatocytes - physiology</topic><topic>Spermatogenesis - genetics</topic><topic>Spermatogenesis - physiology</topic><topic>Transcription</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LA SALLE, Sophie</creatorcontrib><creatorcontrib>PALMER, Kristina</creatorcontrib><creatorcontrib>O'BRIEN, Marilyn</creatorcontrib><creatorcontrib>SCHIMENTI, John C</creatorcontrib><creatorcontrib>EPPIG, John</creatorcontrib><creatorcontrib>HANDEL, Mary Ann</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biology of reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LA SALLE, Sophie</au><au>PALMER, Kristina</au><au>O'BRIEN, Marilyn</au><au>SCHIMENTI, John C</au><au>EPPIG, John</au><au>HANDEL, Mary Ann</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spata22, a Novel Vertebrate-Specific Gene, Is Required for Meiotic Progress in Mouse Germ Cells</atitle><jtitle>Biology of reproduction</jtitle><addtitle>Biol Reprod</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>86</volume><issue>2</issue><spage>45</spage><epage>45</epage><pages>45-45</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><coden>BIREBV</coden><abstract>The N-ethyl-N-nitrosourea-induced repro42 mutation, identified by a forward genetics strategy, causes both male and female infertility, with no other apparent phenotypes. Positional cloning led to the discovery of a nonsense mutation in Spata22, a hitherto uncharacterized gene conserved among bony vertebrates. Expression of both transcript and protein is restricted predominantly to germ cells of both sexes. Germ cells of repro42 mutant mice express Spata22 transcript, but not SPATA22 protein. Gametogenesis is profoundly affected by the mutation, and germ cells in repro42 mutant mice do not progress beyond early meiotic prophase, with subsequent germ cell loss in both males and females. The Spata22 gene is essential for one or more key events of early meiotic prophase, as homologous chromosomes of mutant germ cells do not achieve normal synapsis or repair meiotic DNA double-strand breaks. The repro42 mutation thus identifies a novel mammalian germ cell-specific gene required for meiotic progression.</abstract><cop>Madison, WI</cop><pub>Society for the Study of Reproduction</pub><pmid>22011390</pmid><doi>10.1095/biolreprod.111.095752</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Animals Biological and medical sciences Cell Cycle Proteins - analysis Cell Cycle Proteins - genetics Cell Cycle Proteins - physiology Chromosomes Cloning Codon, Nonsense - genetics DNA damage DNA repair Double-strand break repair Female Fundamental and applied biological sciences. Psychology Gametogenesis Germ cells Infertility Infertility, Female - genetics Infertility, Female - physiopathology Infertility, Male - genetics Infertility, Male - physiopathology Male Meiosis Meiosis - physiology Mice Mice, Inbred C3H Mice, Inbred C57BL Mice, Mutant Strains Molecular Sequence Data Nonsense mutation Oocytes - physiology Oogenesis - genetics Oogenesis - physiology Phenotype Prophase Proteins - analysis Proteins - genetics Proteins - physiology Sex Spermatocytes - physiology Spermatogenesis - genetics Spermatogenesis - physiology Transcription Vertebrates: reproduction |
title | Spata22, a Novel Vertebrate-Specific Gene, Is Required for Meiotic Progress in Mouse Germ Cells |
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