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Temporal and Tissue-Specific Expression of Mouse ets Genes
The expression of ets genes has been studied in mouse tissues and regenerating murine liver, an in vivo model for cell proliferation. Our results indicate that (i) the ets-1 and ets-2 loci are transcriptionally active; (ii) the ets-2 locus encodes a major mRNA (3.5 kilobases) and is expressed in mos...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1987-05, Vol.84 (10), p.3161-3165 |
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creator | Bhat, Narayan K. Fisher, Robert J. Fujiwara, Shigeyoshi Ascione, Richard Papas, Takis S. |
description | The expression of ets genes has been studied in mouse tissues and regenerating murine liver, an in vivo model for cell proliferation. Our results indicate that (i) the ets-1 and ets-2 loci are transcriptionally active; (ii) the ets-2 locus encodes a major mRNA (3.5 kilobases) and is expressed in most of the tissues examined, whereas the ets-1 locus encodes a major 5.3-kilobase and minor 4.0-, 2.5-, and 2.2-kilobase RNA species and is expressed at a high level in thymus; (iii) both ets-1 and ets-2 mRNA are abundant in young proliferating tissues and are greatly reduced in terminally differentiated tissues, except thymus; (iv) compensatory growth of liver induces ets-2 mRNA before DNA synthesis, but after fos and myc induction; and (v) ets-2 mRNA, but not ets-1 mRNA, is stabilized in the presence of cycloheximide during hepatic regeneration. These results suggest that ets-2 gene expression is intrinsically linked with cell proliferation. Thus, ets-2 expression follows a pattern similar to other members of the nuclear oncogene family. During hepatic regeneration, the ets-1 and ets-2 loci are subject to differential regulation. |
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Our results indicate that (i) the ets-1 and ets-2 loci are transcriptionally active; (ii) the ets-2 locus encodes a major mRNA (3.5 kilobases) and is expressed in most of the tissues examined, whereas the ets-1 locus encodes a major 5.3-kilobase and minor 4.0-, 2.5-, and 2.2-kilobase RNA species and is expressed at a high level in thymus; (iii) both ets-1 and ets-2 mRNA are abundant in young proliferating tissues and are greatly reduced in terminally differentiated tissues, except thymus; (iv) compensatory growth of liver induces ets-2 mRNA before DNA synthesis, but after fos and myc induction; and (v) ets-2 mRNA, but not ets-1 mRNA, is stabilized in the presence of cycloheximide during hepatic regeneration. These results suggest that ets-2 gene expression is intrinsically linked with cell proliferation. Thus, ets-2 expression follows a pattern similar to other members of the nuclear oncogene family. During hepatic regeneration, the ets-1 and ets-2 loci are subject to differential regulation.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.84.10.3161</identifier><identifier>PMID: 3472202</identifier><identifier>CODEN: PNASA6</identifier><language>eng</language><publisher>Washington, DC: National Academy of Sciences of the United States of America</publisher><subject>Animals ; Biological and medical sciences ; Cell cycle ; Cell growth ; Chromosomes ; DNA ; DNA Replication ; Fundamental and applied biological sciences. Psychology ; Gene expression ; Genes ; Genetic loci ; Hepatectomy ; Liver ; Liver - analysis ; Liver Regeneration ; Male ; Messenger RNA ; Mice ; Mice, Inbred BALB C ; Molecular and cellular biology ; Molecular genetics ; Molecular Weight ; Oncogenes ; Plasmids ; RNA ; RNA, Messenger - genetics ; RNA, Messenger - isolation & purification ; Tissue Distribution ; Transcription, Genetic</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1987-05, Vol.84 (10), p.3161-3165</ispartof><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-b86ebde0715c2c99c7457166c157a9e6c3dc7c55874c4bc336c75d64258f4f643</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/84/10.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/29352$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/29352$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793,58238,58471</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8300635$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3472202$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bhat, Narayan K.</creatorcontrib><creatorcontrib>Fisher, Robert J.</creatorcontrib><creatorcontrib>Fujiwara, Shigeyoshi</creatorcontrib><creatorcontrib>Ascione, Richard</creatorcontrib><creatorcontrib>Papas, Takis S.</creatorcontrib><title>Temporal and Tissue-Specific Expression of Mouse ets Genes</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The expression of ets genes has been studied in mouse tissues and regenerating murine liver, an in vivo model for cell proliferation. Our results indicate that (i) the ets-1 and ets-2 loci are transcriptionally active; (ii) the ets-2 locus encodes a major mRNA (3.5 kilobases) and is expressed in most of the tissues examined, whereas the ets-1 locus encodes a major 5.3-kilobase and minor 4.0-, 2.5-, and 2.2-kilobase RNA species and is expressed at a high level in thymus; (iii) both ets-1 and ets-2 mRNA are abundant in young proliferating tissues and are greatly reduced in terminally differentiated tissues, except thymus; (iv) compensatory growth of liver induces ets-2 mRNA before DNA synthesis, but after fos and myc induction; and (v) ets-2 mRNA, but not ets-1 mRNA, is stabilized in the presence of cycloheximide during hepatic regeneration. These results suggest that ets-2 gene expression is intrinsically linked with cell proliferation. Thus, ets-2 expression follows a pattern similar to other members of the nuclear oncogene family. During hepatic regeneration, the ets-1 and ets-2 loci are subject to differential regulation.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell cycle</subject><subject>Cell growth</subject><subject>Chromosomes</subject><subject>DNA</subject><subject>DNA Replication</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Genetic loci</subject><subject>Hepatectomy</subject><subject>Liver</subject><subject>Liver - analysis</subject><subject>Liver Regeneration</subject><subject>Male</subject><subject>Messenger RNA</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Weight</subject><subject>Oncogenes</subject><subject>Plasmids</subject><subject>RNA</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - isolation & purification</subject><subject>Tissue Distribution</subject><subject>Transcription, Genetic</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNqFkc1r1UAUxQex1Gd1LQhKFqKrvM73TIQuSqmtUHHhcz3Mm9xoSl4mzk2k_vdOeCHoRleXy_md-8Eh5AWjW0aNOB96j1src7MVTLNHZMNoxUotK_qYbCjlprSSyyfkKeI9pbRSlp6SUyEN55RvyPsdHIaYfFf4vi52LeIE5ZcBQtu0obh-GBIgtrEvYlN8ihNCASMWN9ADPiMnje8Qni_1jHz9cL27ui3vPt98vLq8K4PibCz3VsO-BmqYCjxUVTBSGaZ1YMr4CnQQdTBBKWtkkPsghA5G1VpyZRvZaCnOyMVx7jDtD1AH6Md8rxtSe_Dpl4u-dX8rffvdfYs_naDScpv9bxd_ij8mwNEdWgzQdb6H_JEzRlaWa_1fkEkrhZIig-dHMKSImKBZj2HUzbG4ORZn5dzPsWTHqz9_WPklh6y_WXSPwXdN8n1occWsoFQLlbF3CzbPX9V1j2umrhvhYczk63-SGXh5BO5xjGkleCUUF78BO822GQ</recordid><startdate>19870501</startdate><enddate>19870501</enddate><creator>Bhat, Narayan K.</creator><creator>Fisher, Robert J.</creator><creator>Fujiwara, Shigeyoshi</creator><creator>Ascione, Richard</creator><creator>Papas, Takis S.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><scope>IQODW</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19870501</creationdate><title>Temporal and Tissue-Specific Expression of Mouse ets Genes</title><author>Bhat, Narayan K. ; Fisher, Robert J. ; Fujiwara, Shigeyoshi ; Ascione, Richard ; Papas, Takis S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-b86ebde0715c2c99c7457166c157a9e6c3dc7c55874c4bc336c75d64258f4f643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell cycle</topic><topic>Cell growth</topic><topic>Chromosomes</topic><topic>DNA</topic><topic>DNA Replication</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Genetic loci</topic><topic>Hepatectomy</topic><topic>Liver</topic><topic>Liver - analysis</topic><topic>Liver Regeneration</topic><topic>Male</topic><topic>Messenger RNA</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Weight</topic><topic>Oncogenes</topic><topic>Plasmids</topic><topic>RNA</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - isolation & purification</topic><topic>Tissue Distribution</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bhat, Narayan K.</creatorcontrib><creatorcontrib>Fisher, Robert J.</creatorcontrib><creatorcontrib>Fujiwara, Shigeyoshi</creatorcontrib><creatorcontrib>Ascione, Richard</creatorcontrib><creatorcontrib>Papas, Takis S.</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>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>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>Bhat, Narayan K.</au><au>Fisher, Robert J.</au><au>Fujiwara, Shigeyoshi</au><au>Ascione, Richard</au><au>Papas, Takis S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Temporal and Tissue-Specific Expression of Mouse ets Genes</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1987-05-01</date><risdate>1987</risdate><volume>84</volume><issue>10</issue><spage>3161</spage><epage>3165</epage><pages>3161-3165</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><coden>PNASA6</coden><abstract>The expression of ets genes has been studied in mouse tissues and regenerating murine liver, an in vivo model for cell proliferation. Our results indicate that (i) the ets-1 and ets-2 loci are transcriptionally active; (ii) the ets-2 locus encodes a major mRNA (3.5 kilobases) and is expressed in most of the tissues examined, whereas the ets-1 locus encodes a major 5.3-kilobase and minor 4.0-, 2.5-, and 2.2-kilobase RNA species and is expressed at a high level in thymus; (iii) both ets-1 and ets-2 mRNA are abundant in young proliferating tissues and are greatly reduced in terminally differentiated tissues, except thymus; (iv) compensatory growth of liver induces ets-2 mRNA before DNA synthesis, but after fos and myc induction; and (v) ets-2 mRNA, but not ets-1 mRNA, is stabilized in the presence of cycloheximide during hepatic regeneration. These results suggest that ets-2 gene expression is intrinsically linked with cell proliferation. Thus, ets-2 expression follows a pattern similar to other members of the nuclear oncogene family. During hepatic regeneration, the ets-1 and ets-2 loci are subject to differential regulation.</abstract><cop>Washington, DC</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>3472202</pmid><doi>10.1073/pnas.84.10.3161</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Cell cycle Cell growth Chromosomes DNA DNA Replication Fundamental and applied biological sciences. Psychology Gene expression Genes Genetic loci Hepatectomy Liver Liver - analysis Liver Regeneration Male Messenger RNA Mice Mice, Inbred BALB C Molecular and cellular biology Molecular genetics Molecular Weight Oncogenes Plasmids RNA RNA, Messenger - genetics RNA, Messenger - isolation & purification Tissue Distribution Transcription, Genetic |
title | Temporal and Tissue-Specific Expression of Mouse ets Genes |
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