Dynamics of Maternal Survivin mRNA in Mouse Oocytes and Pre-implantation Embryos
Survivin is a bi-functional protein which has been shown to suppress apoptosis and regulate cell division in mammalian carcinoma cell lines and some somatic cells. In previous studies, we showed that survivin is an essential anti-apoptotic gene which is expressed in mouse pre-implantation embryos, a...
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Veröffentlicht in: | Journal of Mammalian Ova Research 2008-10, Vol.25 (3), p.184-192 |
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creator | Sato, Toshiharu Fukuda, Jun Kawamura, Kazuhiro Kodama, Hideya Kumagai, Jin Tanaka, Toshinobu |
description | Survivin is a bi-functional protein which has been shown to suppress apoptosis and regulate cell division in mammalian carcinoma cell lines and some somatic cells. In previous studies, we showed that survivin is an essential anti-apoptotic gene which is expressed in mouse pre-implantation embryos, and found that embryos in which survivin has been disrupted develop only to the blastocyst stage. Based on what is known about survivin in mammals and other organisms, we proposed that maternal survivin mRNA may be required for oocyte maturation and early embryonic development, including a role in regulation of chromosome segregation. To test this, we assessed changes in survivin mRNA levels over time in mouse oocytes and embryos, and asked if survivin mRNA levels change in a cell cycle-dependent manner in mouse oocytes and embryos. We found that maternal survivin mRNA levels were higher than zygotically transcribed survivin mRNA levels in mouse preimplantation embryos, that zygotic survivin was regulated in a cell-cycle dependent manner, and that survivin mRNA levels were high in young mouse oocytes but decreased as mice aged. Our data suggest that survivin may play a role as a maternal gene in the development of mouse oocytes and pre-implantation embryos. |
doi_str_mv | 10.1274/0916-7625-25.3.184 |
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In previous studies, we showed that survivin is an essential anti-apoptotic gene which is expressed in mouse pre-implantation embryos, and found that embryos in which survivin has been disrupted develop only to the blastocyst stage. Based on what is known about survivin in mammals and other organisms, we proposed that maternal survivin mRNA may be required for oocyte maturation and early embryonic development, including a role in regulation of chromosome segregation. To test this, we assessed changes in survivin mRNA levels over time in mouse oocytes and embryos, and asked if survivin mRNA levels change in a cell cycle-dependent manner in mouse oocytes and embryos. We found that maternal survivin mRNA levels were higher than zygotically transcribed survivin mRNA levels in mouse preimplantation embryos, that zygotic survivin was regulated in a cell-cycle dependent manner, and that survivin mRNA levels were high in young mouse oocytes but decreased as mice aged. Our data suggest that survivin may play a role as a maternal gene in the development of mouse oocytes and pre-implantation embryos.</description><identifier>ISSN: 1341-7738</identifier><identifier>ISSN: 1347-5878</identifier><identifier>EISSN: 1347-5878</identifier><identifier>DOI: 10.1274/0916-7625-25.3.184</identifier><language>eng</language><publisher>Fujisawa: Japanese Society of Mammalian Ova Research</publisher><subject>ANIMAL EMBRYOS ; APOPTOSE ; APOPTOSIS ; EMBRIONES ANIMALES ; Embryo ; EMBRYON ANIMAL ; INHIBICION ; INHIBITION ; MICE ; Originals ; OVA ; OVULE ; OVULO ; PCR ; Quantification ; RATON ; RT-PCR ; Single oocyte ; SOURIS ; Survivin</subject><ispartof>Journal of Mammalian Ova Research, 2008-10, Vol.25 (3), p.184-192</ispartof><rights>2008 Japanese Society of Mammalian Ova Research</rights><rights>Copyright Japan Science and Technology Agency 2008</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-b348t-25b7c7331c33878594cc6e5c86e23bbf91fa6c8a453e0c08624aad014839e65d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://bioone.org/doi/pdf/10.1274/0916-7625-25.3.184$$EPDF$$P50$$Gbioone$$H</linktopdf><link.rule.ids>314,776,780,26957,27903,27904,52341</link.rule.ids></links><search><creatorcontrib>Sato, Toshiharu</creatorcontrib><creatorcontrib>Fukuda, Jun</creatorcontrib><creatorcontrib>Kawamura, Kazuhiro</creatorcontrib><creatorcontrib>Kodama, Hideya</creatorcontrib><creatorcontrib>Kumagai, Jin</creatorcontrib><creatorcontrib>Tanaka, Toshinobu</creatorcontrib><creatorcontrib>Akita University School of Medicine</creatorcontrib><creatorcontrib>Division of Obstetrics and Gynecology</creatorcontrib><creatorcontrib>Department of Reproductive and Developmental Medicine</creatorcontrib><creatorcontrib>Akita University College of Allied Medical Science</creatorcontrib><title>Dynamics of Maternal Survivin mRNA in Mouse Oocytes and Pre-implantation Embryos</title><title>Journal of Mammalian Ova Research</title><description>Survivin is a bi-functional protein which has been shown to suppress apoptosis and regulate cell division in mammalian carcinoma cell lines and some somatic cells. In previous studies, we showed that survivin is an essential anti-apoptotic gene which is expressed in mouse pre-implantation embryos, and found that embryos in which survivin has been disrupted develop only to the blastocyst stage. Based on what is known about survivin in mammals and other organisms, we proposed that maternal survivin mRNA may be required for oocyte maturation and early embryonic development, including a role in regulation of chromosome segregation. To test this, we assessed changes in survivin mRNA levels over time in mouse oocytes and embryos, and asked if survivin mRNA levels change in a cell cycle-dependent manner in mouse oocytes and embryos. We found that maternal survivin mRNA levels were higher than zygotically transcribed survivin mRNA levels in mouse preimplantation embryos, that zygotic survivin was regulated in a cell-cycle dependent manner, and that survivin mRNA levels were high in young mouse oocytes but decreased as mice aged. Our data suggest that survivin may play a role as a maternal gene in the development of mouse oocytes and pre-implantation embryos.</description><subject>ANIMAL EMBRYOS</subject><subject>APOPTOSE</subject><subject>APOPTOSIS</subject><subject>EMBRIONES ANIMALES</subject><subject>Embryo</subject><subject>EMBRYON ANIMAL</subject><subject>INHIBICION</subject><subject>INHIBITION</subject><subject>MICE</subject><subject>Originals</subject><subject>OVA</subject><subject>OVULE</subject><subject>OVULO</subject><subject>PCR</subject><subject>Quantification</subject><subject>RATON</subject><subject>RT-PCR</subject><subject>Single oocyte</subject><subject>SOURIS</subject><subject>Survivin</subject><issn>1341-7738</issn><issn>1347-5878</issn><issn>1347-5878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqNUE1r3DAQNaWFpmn_QKEg6KEnb0ceWZKPIU36QdIs_TgLWSsXBcvaSt7A_vuM64VcC8OMYN578_Sq6i2HDW-U-Agdl7WSTVs37QY3XItn1RlHoepWK_3835vXSqF-Wb0q5R5AaA3qrNp-Ok42BldYGtitnX2e7Mh-HvJDeAgTiz--XzCat-lQPLtL7jj7wuy0Y9vs6xD3o51mO4c0savY52Mqr6sXgx2Lf3Oa59Xv66tfl1_qm7vPXy8vbuoehZ7JZq-cQuQOkRy2nXBO-tZp6Rvs-6Hjg5VOW9GiBwdaNsLaHXChsfOy3eF59X7V3ef09-DLbO7TYTFfDBcCpUZSJVSzolxOpWQ_mH0O0eaj4WCW5MySnFmSM1RoKDkifThJB5-fCJSgWRIkICCckNcrMvpdcHZM0xgm_-TEzTLaGK1pALQBWJgG6DQQm1qHsoMOkITerUKDTcb-yaGYb1sidcSRraI9rPs-pEQX_uMXj8TNmNs</recordid><startdate>200810</startdate><enddate>200810</enddate><creator>Sato, Toshiharu</creator><creator>Fukuda, Jun</creator><creator>Kawamura, Kazuhiro</creator><creator>Kodama, Hideya</creator><creator>Kumagai, Jin</creator><creator>Tanaka, Toshinobu</creator><general>Japanese Society of Mammalian Ova Research</general><general>UniBio Press</general><general>Japan Science and Technology Agency</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>200810</creationdate><title>Dynamics of Maternal Survivin mRNA in Mouse Oocytes and Pre-implantation Embryos</title><author>Sato, Toshiharu ; Fukuda, Jun ; Kawamura, Kazuhiro ; Kodama, Hideya ; Kumagai, Jin ; Tanaka, Toshinobu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b348t-25b7c7331c33878594cc6e5c86e23bbf91fa6c8a453e0c08624aad014839e65d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>ANIMAL EMBRYOS</topic><topic>APOPTOSE</topic><topic>APOPTOSIS</topic><topic>EMBRIONES ANIMALES</topic><topic>Embryo</topic><topic>EMBRYON ANIMAL</topic><topic>INHIBICION</topic><topic>INHIBITION</topic><topic>MICE</topic><topic>Originals</topic><topic>OVA</topic><topic>OVULE</topic><topic>OVULO</topic><topic>PCR</topic><topic>Quantification</topic><topic>RATON</topic><topic>RT-PCR</topic><topic>Single oocyte</topic><topic>SOURIS</topic><topic>Survivin</topic><toplevel>online_resources</toplevel><creatorcontrib>Sato, Toshiharu</creatorcontrib><creatorcontrib>Fukuda, Jun</creatorcontrib><creatorcontrib>Kawamura, Kazuhiro</creatorcontrib><creatorcontrib>Kodama, Hideya</creatorcontrib><creatorcontrib>Kumagai, Jin</creatorcontrib><creatorcontrib>Tanaka, Toshinobu</creatorcontrib><creatorcontrib>Akita University School of Medicine</creatorcontrib><creatorcontrib>Division of Obstetrics and Gynecology</creatorcontrib><creatorcontrib>Department of Reproductive and Developmental Medicine</creatorcontrib><creatorcontrib>Akita University College of Allied Medical Science</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Journal of Mammalian Ova Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sato, Toshiharu</au><au>Fukuda, Jun</au><au>Kawamura, Kazuhiro</au><au>Kodama, Hideya</au><au>Kumagai, Jin</au><au>Tanaka, Toshinobu</au><aucorp>Akita University School of Medicine</aucorp><aucorp>Division of Obstetrics and Gynecology</aucorp><aucorp>Department of Reproductive and Developmental Medicine</aucorp><aucorp>Akita University College of Allied Medical Science</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dynamics of Maternal Survivin mRNA in Mouse Oocytes and Pre-implantation Embryos</atitle><jtitle>Journal of Mammalian Ova Research</jtitle><date>2008-10</date><risdate>2008</risdate><volume>25</volume><issue>3</issue><spage>184</spage><epage>192</epage><pages>184-192</pages><issn>1341-7738</issn><issn>1347-5878</issn><eissn>1347-5878</eissn><abstract>Survivin is a bi-functional protein which has been shown to suppress apoptosis and regulate cell division in mammalian carcinoma cell lines and some somatic cells. In previous studies, we showed that survivin is an essential anti-apoptotic gene which is expressed in mouse pre-implantation embryos, and found that embryos in which survivin has been disrupted develop only to the blastocyst stage. Based on what is known about survivin in mammals and other organisms, we proposed that maternal survivin mRNA may be required for oocyte maturation and early embryonic development, including a role in regulation of chromosome segregation. To test this, we assessed changes in survivin mRNA levels over time in mouse oocytes and embryos, and asked if survivin mRNA levels change in a cell cycle-dependent manner in mouse oocytes and embryos. We found that maternal survivin mRNA levels were higher than zygotically transcribed survivin mRNA levels in mouse preimplantation embryos, that zygotic survivin was regulated in a cell-cycle dependent manner, and that survivin mRNA levels were high in young mouse oocytes but decreased as mice aged. Our data suggest that survivin may play a role as a maternal gene in the development of mouse oocytes and pre-implantation embryos.</abstract><cop>Fujisawa</cop><pub>Japanese Society of Mammalian Ova Research</pub><doi>10.1274/0916-7625-25.3.184</doi><tpages>9</tpages></addata></record> |
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subjects | ANIMAL EMBRYOS APOPTOSE APOPTOSIS EMBRIONES ANIMALES Embryo EMBRYON ANIMAL INHIBICION INHIBITION MICE Originals OVA OVULE OVULO PCR Quantification RATON RT-PCR Single oocyte SOURIS Survivin |
title | Dynamics of Maternal Survivin mRNA in Mouse Oocytes and Pre-implantation Embryos |
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