Regulation of the gonadal transcriptome during sex determination and testis morphogenesis: comparative candidate genes
Gene expression profiles during sex determination and gonadal differentiation were investigated to identify new potential regulatory factors. Embryonic day 13 (E13), E14, and E16 rat testes and ovaries were used for microarray analysis, as well as E13 testis organ cultures that undergo testis morpho...
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description | Gene expression profiles during sex determination and gonadal differentiation were investigated to identify new potential regulatory factors. Embryonic day 13 (E13), E14, and E16 rat testes and ovaries were used for microarray analysis, as well as E13 testis organ cultures that undergo testis morphogenesis and develop seminiferous cords in vitro. A list of 109 genes resulted from a selective analysis for genes present in male gonadal development and with a 1.5-fold change in expression between E13 and E16. Characterization of these 109 genes potentially important for testis development revealed that cytoskeletal-associated proteins, extracellular matrix factors, and signaling factors were highly represented. Throughout the developmental period (E13–E16), sex-enriched transcripts were more prevalent in the male with 34 of the 109 genes having testis-enriched expression during sex determination. In ovaries, the total number of transcripts with a 1.5-fold change in expression between E13 and E16 was similar to the testis, but none of those genes were both ovary enriched and regulated during the developmental period. Genes conserved in sex determination were identified by comparing changing transcripts in the rat analysis herein, to transcripts altered in previously published mouse studies of gonadal sex determination. A comparison of changing mouse and rat transcripts identified 43 genes with species conservation in sex determination and testis development. Profiles of gene expression during E13–E16 rat testis and ovary development are presented and candidate genes for involvement in sex determination and testis differentiation are identified. Analysis of cellular pathways did not reveal any specific pathways involving multiple candidate genes. However, the genes and gene network identified influence numerous cellular processes with cellular differentiation, proliferation, focal contact, RNA localization, and development being predominant. |
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Embryonic day 13 (E13), E14, and E16 rat testes and ovaries were used for microarray analysis, as well as E13 testis organ cultures that undergo testis morphogenesis and develop seminiferous cords in vitro. A list of 109 genes resulted from a selective analysis for genes present in male gonadal development and with a 1.5-fold change in expression between E13 and E16. Characterization of these 109 genes potentially important for testis development revealed that cytoskeletal-associated proteins, extracellular matrix factors, and signaling factors were highly represented. Throughout the developmental period (E13–E16), sex-enriched transcripts were more prevalent in the male with 34 of the 109 genes having testis-enriched expression during sex determination. In ovaries, the total number of transcripts with a 1.5-fold change in expression between E13 and E16 was similar to the testis, but none of those genes were both ovary enriched and regulated during the developmental period. Genes conserved in sex determination were identified by comparing changing transcripts in the rat analysis herein, to transcripts altered in previously published mouse studies of gonadal sex determination. A comparison of changing mouse and rat transcripts identified 43 genes with species conservation in sex determination and testis development. Profiles of gene expression during E13–E16 rat testis and ovary development are presented and candidate genes for involvement in sex determination and testis differentiation are identified. Analysis of cellular pathways did not reveal any specific pathways involving multiple candidate genes. However, the genes and gene network identified influence numerous cellular processes with cellular differentiation, proliferation, focal contact, RNA localization, and development being predominant.</description><identifier>ISSN: 1470-1626</identifier><identifier>EISSN: 1741-7899</identifier><identifier>DOI: 10.1530/REP-06-0341</identifier><identifier>PMID: 17709564</identifier><language>eng</language><publisher>England: Society for Reproduction and Fertility</publisher><subject>animal ovaries ; Animals ; Computational Biology ; embryology ; Embryonic Development ; Embryonic Development - genetics ; extracellular matrix ; Female ; gene expression ; Gene Expression Profiling ; Gene Expression Regulation, Developmental ; Gene Regulatory Networks ; genes ; genetics ; Male ; mice ; microarray technology ; morphogenesis ; Morphogenesis - genetics ; Oligonucleotide Array Sequence Analysis ; Organ Culture Techniques ; ovarian development ; Ovary ; Ovary - embryology ; physiology ; proteins ; Rats ; Rats, Sprague-Dawley ; RNA ; sex determination ; Sex Determination Processes ; Sex Differentiation ; testes ; Testis ; Testis - embryology ; Transcription, Genetic ; Transcription, Genetic - physiology ; transcriptome</subject><ispartof>Reproduction (Cambridge, England), 2007-09, Vol.134 (3), p.455-472</ispartof><rights>2007 Society for Reproduction and Fertility</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b582t-9b950cfe363442618f1fb0d8886e28985f00ace93d4d6cc1e551a285d2e355853</citedby><cites>FETCH-LOGICAL-b582t-9b950cfe363442618f1fb0d8886e28985f00ace93d4d6cc1e551a285d2e355853</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17709564$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Clement, Tracy M</creatorcontrib><creatorcontrib>Anway, Matthew D</creatorcontrib><creatorcontrib>Uzumcu, Mehmet</creatorcontrib><creatorcontrib>Skinner, Michael K</creatorcontrib><title>Regulation of the gonadal transcriptome during sex determination and testis morphogenesis: comparative candidate genes</title><title>Reproduction (Cambridge, England)</title><addtitle>Reproduction</addtitle><description>Gene expression profiles during sex determination and gonadal differentiation were investigated to identify new potential regulatory factors. Embryonic day 13 (E13), E14, and E16 rat testes and ovaries were used for microarray analysis, as well as E13 testis organ cultures that undergo testis morphogenesis and develop seminiferous cords in vitro. A list of 109 genes resulted from a selective analysis for genes present in male gonadal development and with a 1.5-fold change in expression between E13 and E16. Characterization of these 109 genes potentially important for testis development revealed that cytoskeletal-associated proteins, extracellular matrix factors, and signaling factors were highly represented. Throughout the developmental period (E13–E16), sex-enriched transcripts were more prevalent in the male with 34 of the 109 genes having testis-enriched expression during sex determination. In ovaries, the total number of transcripts with a 1.5-fold change in expression between E13 and E16 was similar to the testis, but none of those genes were both ovary enriched and regulated during the developmental period. Genes conserved in sex determination were identified by comparing changing transcripts in the rat analysis herein, to transcripts altered in previously published mouse studies of gonadal sex determination. A comparison of changing mouse and rat transcripts identified 43 genes with species conservation in sex determination and testis development. Profiles of gene expression during E13–E16 rat testis and ovary development are presented and candidate genes for involvement in sex determination and testis differentiation are identified. Analysis of cellular pathways did not reveal any specific pathways involving multiple candidate genes. However, the genes and gene network identified influence numerous cellular processes with cellular differentiation, proliferation, focal contact, RNA localization, and development being predominant.</description><subject>animal ovaries</subject><subject>Animals</subject><subject>Computational Biology</subject><subject>embryology</subject><subject>Embryonic Development</subject><subject>Embryonic Development - genetics</subject><subject>extracellular matrix</subject><subject>Female</subject><subject>gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Gene Regulatory Networks</subject><subject>genes</subject><subject>genetics</subject><subject>Male</subject><subject>mice</subject><subject>microarray technology</subject><subject>morphogenesis</subject><subject>Morphogenesis - genetics</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Organ Culture Techniques</subject><subject>ovarian development</subject><subject>Ovary</subject><subject>Ovary - embryology</subject><subject>physiology</subject><subject>proteins</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA</subject><subject>sex determination</subject><subject>Sex Determination Processes</subject><subject>Sex Differentiation</subject><subject>testes</subject><subject>Testis</subject><subject>Testis - embryology</subject><subject>Transcription, Genetic</subject><subject>Transcription, Genetic - physiology</subject><subject>transcriptome</subject><issn>1470-1626</issn><issn>1741-7899</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks1v1TAQxCMEoqVw4g4-cakCazt2HA6VUFU-pEqgQs-W42wSoyR-2MmD_vc4ygMKB3qypf3NaMfjLHtK4SUVHF5dXXzKQebAC3ovO6ZlQfNSVdX9dC9KyKlk8ih7FONXACpUKR9mR7QsoRKyOM72V9gtg5mdn4hvydwj6fxkGjOQOZgp2uB2sx-RNEtwU0ci_iANzhhGN20qMzVkxji7SEYfdr3vcMLo4mti_bgzIVF7JDZhrjFzsl_Hj7MHrRkiPjmcJ9n124sv5-_zy4_vPpy_ucxrodicV3UlwLbIJS8KJqlqaVtDo5SSyFSlRAtgLFa8KRppLUUhqGFKNAy5EErwk-xs890t9YiNxSmlGvQuuNGEG-2N039PJtfrzu-1YhIAVDJ4cTAI_tuSYurRRYvDYCb0S9RSUSVkye8Ei9QLh7K4E2TAZcHE6ni6gTb4GAO2v9emoNfmdWpeg9Rr84l-djvpH_ZQdQLYBvSu67-7gLp2PlqXgrvWWXPb9dd_SqLnm6g1XpsuuKivPzNISUABiGp9YboR_7j9b9efb1fVwA</recordid><startdate>20070901</startdate><enddate>20070901</enddate><creator>Clement, Tracy M</creator><creator>Anway, Matthew D</creator><creator>Uzumcu, Mehmet</creator><creator>Skinner, Michael K</creator><general>Society for Reproduction and Fertility</general><general>BioScientifica Ltd</general><scope>FBQ</scope><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>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7S9</scope><scope>L.6</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20070901</creationdate><title>Regulation of the gonadal transcriptome during sex determination and testis morphogenesis: comparative candidate genes</title><author>Clement, Tracy M ; Anway, Matthew D ; Uzumcu, Mehmet ; Skinner, Michael K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b582t-9b950cfe363442618f1fb0d8886e28985f00ace93d4d6cc1e551a285d2e355853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>animal ovaries</topic><topic>Animals</topic><topic>Computational Biology</topic><topic>embryology</topic><topic>Embryonic Development</topic><topic>Embryonic Development - genetics</topic><topic>extracellular matrix</topic><topic>Female</topic><topic>gene expression</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Gene Regulatory Networks</topic><topic>genes</topic><topic>genetics</topic><topic>Male</topic><topic>mice</topic><topic>microarray technology</topic><topic>morphogenesis</topic><topic>Morphogenesis - genetics</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Organ Culture Techniques</topic><topic>ovarian development</topic><topic>Ovary</topic><topic>Ovary - embryology</topic><topic>physiology</topic><topic>proteins</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA</topic><topic>sex determination</topic><topic>Sex Determination Processes</topic><topic>Sex Differentiation</topic><topic>testes</topic><topic>Testis</topic><topic>Testis - embryology</topic><topic>Transcription, Genetic</topic><topic>Transcription, Genetic - physiology</topic><topic>transcriptome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Clement, Tracy M</creatorcontrib><creatorcontrib>Anway, Matthew D</creatorcontrib><creatorcontrib>Uzumcu, Mehmet</creatorcontrib><creatorcontrib>Skinner, Michael K</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Reproduction (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Clement, Tracy M</au><au>Anway, Matthew D</au><au>Uzumcu, Mehmet</au><au>Skinner, Michael K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of the gonadal transcriptome during sex determination and testis morphogenesis: comparative candidate genes</atitle><jtitle>Reproduction (Cambridge, England)</jtitle><addtitle>Reproduction</addtitle><date>2007-09-01</date><risdate>2007</risdate><volume>134</volume><issue>3</issue><spage>455</spage><epage>472</epage><pages>455-472</pages><issn>1470-1626</issn><eissn>1741-7899</eissn><abstract>Gene expression profiles during sex determination and gonadal differentiation were investigated to identify new potential regulatory factors. Embryonic day 13 (E13), E14, and E16 rat testes and ovaries were used for microarray analysis, as well as E13 testis organ cultures that undergo testis morphogenesis and develop seminiferous cords in vitro. A list of 109 genes resulted from a selective analysis for genes present in male gonadal development and with a 1.5-fold change in expression between E13 and E16. Characterization of these 109 genes potentially important for testis development revealed that cytoskeletal-associated proteins, extracellular matrix factors, and signaling factors were highly represented. Throughout the developmental period (E13–E16), sex-enriched transcripts were more prevalent in the male with 34 of the 109 genes having testis-enriched expression during sex determination. In ovaries, the total number of transcripts with a 1.5-fold change in expression between E13 and E16 was similar to the testis, but none of those genes were both ovary enriched and regulated during the developmental period. Genes conserved in sex determination were identified by comparing changing transcripts in the rat analysis herein, to transcripts altered in previously published mouse studies of gonadal sex determination. A comparison of changing mouse and rat transcripts identified 43 genes with species conservation in sex determination and testis development. Profiles of gene expression during E13–E16 rat testis and ovary development are presented and candidate genes for involvement in sex determination and testis differentiation are identified. Analysis of cellular pathways did not reveal any specific pathways involving multiple candidate genes. However, the genes and gene network identified influence numerous cellular processes with cellular differentiation, proliferation, focal contact, RNA localization, and development being predominant.</abstract><cop>England</cop><pub>Society for Reproduction and Fertility</pub><pmid>17709564</pmid><doi>10.1530/REP-06-0341</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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subjects | animal ovaries Animals Computational Biology embryology Embryonic Development Embryonic Development - genetics extracellular matrix Female gene expression Gene Expression Profiling Gene Expression Regulation, Developmental Gene Regulatory Networks genes genetics Male mice microarray technology morphogenesis Morphogenesis - genetics Oligonucleotide Array Sequence Analysis Organ Culture Techniques ovarian development Ovary Ovary - embryology physiology proteins Rats Rats, Sprague-Dawley RNA sex determination Sex Determination Processes Sex Differentiation testes Testis Testis - embryology Transcription, Genetic Transcription, Genetic - physiology transcriptome |
title | Regulation of the gonadal transcriptome during sex determination and testis morphogenesis: comparative candidate genes |
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