GASZ is essential for male meiosis and suppression of retrotransposon expression in the male germline
Nuage are amorphous ultrastructural granules in the cytoplasm of male germ cells as divergent as Drosophila, Xenopus, and Homo sapiens. Most nuage are cytoplasmic ribonucleoprotein structures implicated in diverse RNA metabolism including the regulation of PIWI-interacting RNA (piRNA) synthesis by t...
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creator | Ma, Lang Buchold, Gregory M Greenbaum, Michael P Roy, Angshumoy Burns, Kathleen H Zhu, Huifeng Han, Derek Y Harris, R Alan Coarfa, Cristian Gunaratne, Preethi H Yan, Wei Matzuk, Martin M |
description | Nuage are amorphous ultrastructural granules in the cytoplasm of male germ cells as divergent as Drosophila, Xenopus, and Homo sapiens. Most nuage are cytoplasmic ribonucleoprotein structures implicated in diverse RNA metabolism including the regulation of PIWI-interacting RNA (piRNA) synthesis by the PIWI family (i.e., MILI, MIWI2, and MIWI). MILI is prominent in embryonic and early post-natal germ cells in nuage also called germinal granules that are often associated with mitochondria and called intermitochondrial cement. We find that GASZ (Germ cell protein with Ankyrin repeats, Sterile alpha motif, and leucine Zipper) co-localizes with MILI in intermitochondrial cement. Knockout of Gasz in mice results in a dramatic downregulation of MILI, and phenocopies the zygotene-pachytene spermatocyte block and male sterility defect observed in MILI null mice. In Gasz null testes, we observe increased hypomethylation and expression of retrotransposons similar to MILI null testes. We also find global shifts in the small RNAome, including down-regulation of repeat-associated, known, and novel piRNAs. These studies provide the first evidence for an essential structural role for GASZ in male fertility and epigenetic and post-transcriptional silencing of retrotransposons by stabilizing MILI in nuage. |
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Most nuage are cytoplasmic ribonucleoprotein structures implicated in diverse RNA metabolism including the regulation of PIWI-interacting RNA (piRNA) synthesis by the PIWI family (i.e., MILI, MIWI2, and MIWI). MILI is prominent in embryonic and early post-natal germ cells in nuage also called germinal granules that are often associated with mitochondria and called intermitochondrial cement. We find that GASZ (Germ cell protein with Ankyrin repeats, Sterile alpha motif, and leucine Zipper) co-localizes with MILI in intermitochondrial cement. Knockout of Gasz in mice results in a dramatic downregulation of MILI, and phenocopies the zygotene-pachytene spermatocyte block and male sterility defect observed in MILI null mice. In Gasz null testes, we observe increased hypomethylation and expression of retrotransposons similar to MILI null testes. We also find global shifts in the small RNAome, including down-regulation of repeat-associated, known, and novel piRNAs. These studies provide the first evidence for an essential structural role for GASZ in male fertility and epigenetic and post-transcriptional silencing of retrotransposons by stabilizing MILI in nuage.</description><identifier>ISSN: 1553-7404</identifier><identifier>ISSN: 1553-7390</identifier><identifier>EISSN: 1553-7404</identifier><identifier>DOI: 10.1371/journal.pgen.1000635</identifier><identifier>PMID: 19730684</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adaptor Proteins, Signal Transducing - genetics ; Adaptor Proteins, Signal Transducing - metabolism ; Animals ; Argonaute Proteins ; Cell Biology/Developmental Molecular Mechanisms ; Cement ; Developmental Biology/Developmental Molecular Mechanisms ; Developmental Biology/Germ Cells ; DNA damage ; DNA methylation ; Down-Regulation ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Epigenetics ; Female ; Genetics and Genomics/Animal Genetics ; Genetics and Genomics/Epigenetics ; Infertility ; Infertility, Male - genetics ; Infertility, Male - metabolism ; Male ; Meiosis ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Microscopy ; Molecular Biology/RNA-Protein Interactions ; Physiological aspects ; Proteins ; Proteins - genetics ; Proteins - metabolism ; Retroelements ; Retrotransposons ; RNA ; RNA, Small Interfering - genetics ; RNA, Small Interfering - metabolism ; Spermatozoa - cytology ; Spermatozoa - metabolism ; Studies</subject><ispartof>PLoS genetics, 2009-09, Vol.5 (9), p.e1000635-e1000635</ispartof><rights>COPYRIGHT 2009 Public Library of Science</rights><rights>Ma et al. 2009</rights><rights>2009 Ma et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Ma L, Buchold GM, Greenbaum MP, Roy A, Burns KH, et al. (2009) GASZ Is Essential for Male Meiosis and Suppression of Retrotransposon Expression in the Male Germline. PLoS Genet 5(9): e1000635. doi:10.1371/journal.pgen.1000635</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c762t-f3a3a464e3e357d4db1febbacd570487f012201c082f29923bfefb7a7f21701a3</citedby><cites>FETCH-LOGICAL-c762t-f3a3a464e3e357d4db1febbacd570487f012201c082f29923bfefb7a7f21701a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2727916/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2727916/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19730684$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ma, Lang</creatorcontrib><creatorcontrib>Buchold, Gregory M</creatorcontrib><creatorcontrib>Greenbaum, Michael P</creatorcontrib><creatorcontrib>Roy, Angshumoy</creatorcontrib><creatorcontrib>Burns, Kathleen H</creatorcontrib><creatorcontrib>Zhu, Huifeng</creatorcontrib><creatorcontrib>Han, Derek Y</creatorcontrib><creatorcontrib>Harris, R Alan</creatorcontrib><creatorcontrib>Coarfa, Cristian</creatorcontrib><creatorcontrib>Gunaratne, Preethi H</creatorcontrib><creatorcontrib>Yan, Wei</creatorcontrib><creatorcontrib>Matzuk, Martin M</creatorcontrib><title>GASZ is essential for male meiosis and suppression of retrotransposon expression in the male germline</title><title>PLoS genetics</title><addtitle>PLoS Genet</addtitle><description>Nuage are amorphous ultrastructural granules in the cytoplasm of male germ cells as divergent as Drosophila, Xenopus, and Homo sapiens. Most nuage are cytoplasmic ribonucleoprotein structures implicated in diverse RNA metabolism including the regulation of PIWI-interacting RNA (piRNA) synthesis by the PIWI family (i.e., MILI, MIWI2, and MIWI). MILI is prominent in embryonic and early post-natal germ cells in nuage also called germinal granules that are often associated with mitochondria and called intermitochondrial cement. We find that GASZ (Germ cell protein with Ankyrin repeats, Sterile alpha motif, and leucine Zipper) co-localizes with MILI in intermitochondrial cement. Knockout of Gasz in mice results in a dramatic downregulation of MILI, and phenocopies the zygotene-pachytene spermatocyte block and male sterility defect observed in MILI null mice. In Gasz null testes, we observe increased hypomethylation and expression of retrotransposons similar to MILI null testes. We also find global shifts in the small RNAome, including down-regulation of repeat-associated, known, and novel piRNAs. These studies provide the first evidence for an essential structural role for GASZ in male fertility and epigenetic and post-transcriptional silencing of retrotransposons by stabilizing MILI in nuage.</description><subject>Adaptor Proteins, Signal Transducing - genetics</subject><subject>Adaptor Proteins, Signal Transducing - metabolism</subject><subject>Animals</subject><subject>Argonaute Proteins</subject><subject>Cell Biology/Developmental Molecular Mechanisms</subject><subject>Cement</subject><subject>Developmental Biology/Developmental Molecular Mechanisms</subject><subject>Developmental Biology/Germ Cells</subject><subject>DNA damage</subject><subject>DNA methylation</subject><subject>Down-Regulation</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>Epigenetics</subject><subject>Female</subject><subject>Genetics and Genomics/Animal Genetics</subject><subject>Genetics and Genomics/Epigenetics</subject><subject>Infertility</subject><subject>Infertility, Male - genetics</subject><subject>Infertility, Male - metabolism</subject><subject>Male</subject><subject>Meiosis</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Microscopy</subject><subject>Molecular Biology/RNA-Protein Interactions</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Proteins - genetics</subject><subject>Proteins - metabolism</subject><subject>Retroelements</subject><subject>Retrotransposons</subject><subject>RNA</subject><subject>RNA, Small Interfering - genetics</subject><subject>RNA, Small Interfering - metabolism</subject><subject>Spermatozoa - cytology</subject><subject>Spermatozoa - metabolism</subject><subject>Studies</subject><issn>1553-7404</issn><issn>1553-7390</issn><issn>1553-7404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNqVk12L1DAUhoso7rr6D0QLwoIXM-arTXsjDIuuA4sLrnrhTUjbk06GNOkmraz_3oyt6xS8UHKRcM5z3kPe5CTJc4zWmHL8Zu9Gb6VZ9y3YNUYI5TR7kJziLKMrzhB7eHQ-SZ6EsEeIZkXJHycnuOQU5QU7TeByc_Mt1SGFEMAOWppUOZ920kDagXYhpqRt0jD2vY-MdjZ1KvUweDd4aUPvQgzB3X1W23TYwaTQgu-MtvA0eaSkCfBs3s-SL-_ffb74sLq6vtxebK5WNc_JsFJUUslyBhRoxhvWVFhBVcm6yThiBVcIE4JwjQqiSFkSWilQFZdcEcwRlvQseTnp9sYFMTsUBKaYZqzIcx6J7UQ0Tu5F73Un_Q_hpBa_As63QvpB1wZEg7kqcYMVbwgrYsO6UBiXZVlJIjmHqPV27jZWHTR19M9LsxBdZqzeidZ9F4QTXuI8CpzPAt7djhAG0elQgzHSghuDyHlOGSIsgq8msI2uCm3Vwfv6AItNvDrNSZaRSK3_QsXVQKdrZ0HpGF8UvF4URGaAu6GVYwhie_PpP9iP_85ef12y50fsDqQZdsGZcYh_KSxBNoG1dyF4UPdGYyQOE_H7vcVhIsQ8EbHsxfEj_SmaR4D-BCmNBv4</recordid><startdate>20090901</startdate><enddate>20090901</enddate><creator>Ma, Lang</creator><creator>Buchold, Gregory M</creator><creator>Greenbaum, Michael P</creator><creator>Roy, Angshumoy</creator><creator>Burns, Kathleen H</creator><creator>Zhu, Huifeng</creator><creator>Han, Derek Y</creator><creator>Harris, R Alan</creator><creator>Coarfa, Cristian</creator><creator>Gunaratne, Preethi H</creator><creator>Yan, Wei</creator><creator>Matzuk, Martin M</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISN</scope><scope>ISR</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20090901</creationdate><title>GASZ is essential for male meiosis and suppression of retrotransposon expression in the male germline</title><author>Ma, Lang ; Buchold, Gregory M ; Greenbaum, Michael P ; Roy, Angshumoy ; Burns, Kathleen H ; Zhu, Huifeng ; Han, Derek Y ; Harris, R Alan ; Coarfa, Cristian ; Gunaratne, Preethi H ; Yan, Wei ; Matzuk, Martin M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c762t-f3a3a464e3e357d4db1febbacd570487f012201c082f29923bfefb7a7f21701a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adaptor Proteins, Signal Transducing - genetics</topic><topic>Adaptor Proteins, Signal Transducing - metabolism</topic><topic>Animals</topic><topic>Argonaute Proteins</topic><topic>Cell Biology/Developmental Molecular Mechanisms</topic><topic>Cement</topic><topic>Developmental Biology/Developmental Molecular Mechanisms</topic><topic>Developmental Biology/Germ Cells</topic><topic>DNA damage</topic><topic>DNA methylation</topic><topic>Down-Regulation</topic><topic>Drosophila Proteins - genetics</topic><topic>Drosophila Proteins - metabolism</topic><topic>Epigenetics</topic><topic>Female</topic><topic>Genetics and Genomics/Animal Genetics</topic><topic>Genetics and Genomics/Epigenetics</topic><topic>Infertility</topic><topic>Infertility, Male - genetics</topic><topic>Infertility, Male - metabolism</topic><topic>Male</topic><topic>Meiosis</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Microscopy</topic><topic>Molecular Biology/RNA-Protein Interactions</topic><topic>Physiological aspects</topic><topic>Proteins</topic><topic>Proteins - genetics</topic><topic>Proteins - metabolism</topic><topic>Retroelements</topic><topic>Retrotransposons</topic><topic>RNA</topic><topic>RNA, Small Interfering - genetics</topic><topic>RNA, Small Interfering - metabolism</topic><topic>Spermatozoa - cytology</topic><topic>Spermatozoa - metabolism</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ma, Lang</creatorcontrib><creatorcontrib>Buchold, Gregory M</creatorcontrib><creatorcontrib>Greenbaum, Michael P</creatorcontrib><creatorcontrib>Roy, Angshumoy</creatorcontrib><creatorcontrib>Burns, Kathleen H</creatorcontrib><creatorcontrib>Zhu, Huifeng</creatorcontrib><creatorcontrib>Han, Derek Y</creatorcontrib><creatorcontrib>Harris, R Alan</creatorcontrib><creatorcontrib>Coarfa, Cristian</creatorcontrib><creatorcontrib>Gunaratne, Preethi H</creatorcontrib><creatorcontrib>Yan, Wei</creatorcontrib><creatorcontrib>Matzuk, Martin M</creatorcontrib><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>MEDLINE - Academic</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>Ma, Lang</au><au>Buchold, Gregory M</au><au>Greenbaum, Michael P</au><au>Roy, Angshumoy</au><au>Burns, Kathleen H</au><au>Zhu, Huifeng</au><au>Han, Derek Y</au><au>Harris, R Alan</au><au>Coarfa, Cristian</au><au>Gunaratne, Preethi H</au><au>Yan, Wei</au><au>Matzuk, Martin M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GASZ is essential for male meiosis and suppression of retrotransposon expression in the male germline</atitle><jtitle>PLoS genetics</jtitle><addtitle>PLoS Genet</addtitle><date>2009-09-01</date><risdate>2009</risdate><volume>5</volume><issue>9</issue><spage>e1000635</spage><epage>e1000635</epage><pages>e1000635-e1000635</pages><issn>1553-7404</issn><issn>1553-7390</issn><eissn>1553-7404</eissn><abstract>Nuage are amorphous ultrastructural granules in the cytoplasm of male germ cells as divergent as Drosophila, Xenopus, and Homo sapiens. Most nuage are cytoplasmic ribonucleoprotein structures implicated in diverse RNA metabolism including the regulation of PIWI-interacting RNA (piRNA) synthesis by the PIWI family (i.e., MILI, MIWI2, and MIWI). MILI is prominent in embryonic and early post-natal germ cells in nuage also called germinal granules that are often associated with mitochondria and called intermitochondrial cement. We find that GASZ (Germ cell protein with Ankyrin repeats, Sterile alpha motif, and leucine Zipper) co-localizes with MILI in intermitochondrial cement. Knockout of Gasz in mice results in a dramatic downregulation of MILI, and phenocopies the zygotene-pachytene spermatocyte block and male sterility defect observed in MILI null mice. In Gasz null testes, we observe increased hypomethylation and expression of retrotransposons similar to MILI null testes. We also find global shifts in the small RNAome, including down-regulation of repeat-associated, known, and novel piRNAs. These studies provide the first evidence for an essential structural role for GASZ in male fertility and epigenetic and post-transcriptional silencing of retrotransposons by stabilizing MILI in nuage.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>19730684</pmid><doi>10.1371/journal.pgen.1000635</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adaptor Proteins, Signal Transducing - genetics Adaptor Proteins, Signal Transducing - metabolism Animals Argonaute Proteins Cell Biology/Developmental Molecular Mechanisms Cement Developmental Biology/Developmental Molecular Mechanisms Developmental Biology/Germ Cells DNA damage DNA methylation Down-Regulation Drosophila Proteins - genetics Drosophila Proteins - metabolism Epigenetics Female Genetics and Genomics/Animal Genetics Genetics and Genomics/Epigenetics Infertility Infertility, Male - genetics Infertility, Male - metabolism Male Meiosis Mice Mice, Inbred C57BL Mice, Knockout Microscopy Molecular Biology/RNA-Protein Interactions Physiological aspects Proteins Proteins - genetics Proteins - metabolism Retroelements Retrotransposons RNA RNA, Small Interfering - genetics RNA, Small Interfering - metabolism Spermatozoa - cytology Spermatozoa - metabolism Studies |
title | GASZ is essential for male meiosis and suppression of retrotransposon expression in the male germline |
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