Translational regulation of a specific gene during oogenesis and embryogenesis of Drosophila
Polysomal and postpolysomal mRNAs were prepared from Drosophila egg chambers or embryos of different developmental stages. Cell-free translation of these mRNAs followed by two-dimensional gel electrophoresis of the products indicated the presence of a specific mRNA that appears to be translated (pol...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1983-06, Vol.80 (11), p.3359-3363 |
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creator | Fruscoloni, P Al-Atia, G.R Jacobs-Lorena, M |
description | Polysomal and postpolysomal mRNAs were prepared from Drosophila egg chambers or embryos of different developmental stages. Cell-free translation of these mRNAs followed by two-dimensional gel electrophoresis of the products indicated the presence of a specific mRNA that appears to be translated (polysome-associated) during oogenesis. This mRNA, designated T1 mRNA, is selectively excluded from polysomes in 3-hr- and 5-hr-old embryos and is again translated in 18-hr-old embryos. A clone containing DNA complementary to T1 mRNA was selected from a library of recombinant DNA prepared from polyadenylylated ovary RNA. This clone was positively identified by hybrid-selected translation followed by two-dimensional gel electrophoresis and autoradiography. T1 mRNA is polyadenylylated and codes for a small, acidic protein. The cloned probe hybridizes to a unique site (2L-39CD) of the polytene chromosomes, very close to the histone genes. The results suggest that this mRNA is under specific translational regulation in contrast to a background of a large number of other abundant mRNAs that are translated at all developmental stages examined. |
doi_str_mv | 10.1073/pnas.80.11.3359 |
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Cell-free translation of these mRNAs followed by two-dimensional gel electrophoresis of the products indicated the presence of a specific mRNA that appears to be translated (polysome-associated) during oogenesis. This mRNA, designated T1 mRNA, is selectively excluded from polysomes in 3-hr- and 5-hr-old embryos and is again translated in 18-hr-old embryos. A clone containing DNA complementary to T1 mRNA was selected from a library of recombinant DNA prepared from polyadenylylated ovary RNA. This clone was positively identified by hybrid-selected translation followed by two-dimensional gel electrophoresis and autoradiography. T1 mRNA is polyadenylylated and codes for a small, acidic protein. The cloned probe hybridizes to a unique site (2L-39CD) of the polytene chromosomes, very close to the histone genes. The results suggest that this mRNA is under specific translational regulation in contrast to a background of a large number of other abundant mRNAs that are translated at all developmental stages examined.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.80.11.3359</identifier><identifier>PMID: 16593324</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>animal reproduction ; arthropods ; Biological Sciences: Developmental Biology ; DNA ; Eggs ; Embryos ; entomology ; Gels ; Gene expression regulation ; Genes ; Messenger RNA ; Oogenesis ; Polyribosomes ; RNA</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1983-06, Vol.80 (11), p.3359-3363</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c487t-a1b4255053c114fd913ab6e83259db6ff7cdb8f74e9ed1b9a7b1015ac76f43a43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/80/11.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/14533$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/14533$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16593324$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fruscoloni, P</creatorcontrib><creatorcontrib>Al-Atia, G.R</creatorcontrib><creatorcontrib>Jacobs-Lorena, M</creatorcontrib><title>Translational regulation of a specific gene during oogenesis and embryogenesis of Drosophila</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Polysomal and postpolysomal mRNAs were prepared from Drosophila egg chambers or embryos of different developmental stages. Cell-free translation of these mRNAs followed by two-dimensional gel electrophoresis of the products indicated the presence of a specific mRNA that appears to be translated (polysome-associated) during oogenesis. This mRNA, designated T1 mRNA, is selectively excluded from polysomes in 3-hr- and 5-hr-old embryos and is again translated in 18-hr-old embryos. A clone containing DNA complementary to T1 mRNA was selected from a library of recombinant DNA prepared from polyadenylylated ovary RNA. This clone was positively identified by hybrid-selected translation followed by two-dimensional gel electrophoresis and autoradiography. T1 mRNA is polyadenylylated and codes for a small, acidic protein. The cloned probe hybridizes to a unique site (2L-39CD) of the polytene chromosomes, very close to the histone genes. The results suggest that this mRNA is under specific translational regulation in contrast to a background of a large number of other abundant mRNAs that are translated at all developmental stages examined.</description><subject>animal reproduction</subject><subject>arthropods</subject><subject>Biological Sciences: Developmental Biology</subject><subject>DNA</subject><subject>Eggs</subject><subject>Embryos</subject><subject>entomology</subject><subject>Gels</subject><subject>Gene expression regulation</subject><subject>Genes</subject><subject>Messenger RNA</subject><subject>Oogenesis</subject><subject>Polyribosomes</subject><subject>RNA</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><recordid>eNptUUtv1DAYtBAVXQpnJA7gG6ds7dhO7AMHVF6VKnGgvSFZXxI7dZW1g50g-u9xlKW7lXqyxjPzvQahN5RsKanZ-eghbWUGdMuYUM_QhhJFi4or8hxtCCnrQvKSn6KXKd0RQpSQ5AU6pZVQjJV8g35dR_BpgMkFDwOOpp9XgIPFgNNoWmddi3vjDe7m6HyPQ1hQcgmD77DZNfH-4Se7PseQwnjrBniFTiwMybzev2fo5uuX64vvxdWPb5cXn66Klst6KoA2vBSCCNZSym2nKIOmMpKVQnVNZW3ddo20NTfKdLRRUDeUUAFtXVnOgLMz9HGtO87NznSt8VOEQY_R7SDe6wBOP2a8u9V9-KOZ4oSX2f9h74_h92zSpHcutWYYwJswJ13n2-bpBM3K81XZ5iVTNPahCSV6SUQviWiZAdVLItnx7ni2g34fwVHzxfmfPlTQdh6Gyfydjko9rcyCt6vgLk0hHlpxwVgm36-khaChjy7pm58loYzkM0spCfsHXki0XA</recordid><startdate>19830601</startdate><enddate>19830601</enddate><creator>Fruscoloni, P</creator><creator>Al-Atia, G.R</creator><creator>Jacobs-Lorena, M</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><scope>FBQ</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19830601</creationdate><title>Translational regulation of a specific gene during oogenesis and embryogenesis of Drosophila</title><author>Fruscoloni, P ; Al-Atia, G.R ; Jacobs-Lorena, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-a1b4255053c114fd913ab6e83259db6ff7cdb8f74e9ed1b9a7b1015ac76f43a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>animal reproduction</topic><topic>arthropods</topic><topic>Biological Sciences: Developmental Biology</topic><topic>DNA</topic><topic>Eggs</topic><topic>Embryos</topic><topic>entomology</topic><topic>Gels</topic><topic>Gene expression regulation</topic><topic>Genes</topic><topic>Messenger RNA</topic><topic>Oogenesis</topic><topic>Polyribosomes</topic><topic>RNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fruscoloni, P</creatorcontrib><creatorcontrib>Al-Atia, G.R</creatorcontrib><creatorcontrib>Jacobs-Lorena, M</creatorcontrib><collection>AGRIS</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fruscoloni, P</au><au>Al-Atia, G.R</au><au>Jacobs-Lorena, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Translational regulation of a specific gene during oogenesis and embryogenesis of Drosophila</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1983-06-01</date><risdate>1983</risdate><volume>80</volume><issue>11</issue><spage>3359</spage><epage>3363</epage><pages>3359-3363</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Polysomal and postpolysomal mRNAs were prepared from Drosophila egg chambers or embryos of different developmental stages. Cell-free translation of these mRNAs followed by two-dimensional gel electrophoresis of the products indicated the presence of a specific mRNA that appears to be translated (polysome-associated) during oogenesis. This mRNA, designated T1 mRNA, is selectively excluded from polysomes in 3-hr- and 5-hr-old embryos and is again translated in 18-hr-old embryos. A clone containing DNA complementary to T1 mRNA was selected from a library of recombinant DNA prepared from polyadenylylated ovary RNA. This clone was positively identified by hybrid-selected translation followed by two-dimensional gel electrophoresis and autoradiography. T1 mRNA is polyadenylylated and codes for a small, acidic protein. The cloned probe hybridizes to a unique site (2L-39CD) of the polytene chromosomes, very close to the histone genes. The results suggest that this mRNA is under specific translational regulation in contrast to a background of a large number of other abundant mRNAs that are translated at all developmental stages examined.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>16593324</pmid><doi>10.1073/pnas.80.11.3359</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | Jstor Complete Legacy; PubMed Central Free; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | animal reproduction arthropods Biological Sciences: Developmental Biology DNA Eggs Embryos entomology Gels Gene expression regulation Genes Messenger RNA Oogenesis Polyribosomes RNA |
title | Translational regulation of a specific gene during oogenesis and embryogenesis of Drosophila |
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