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Modulation of the Transferred Mouse 26K Casein Gene in Mouse L Cells by Glucocorticoid Hormone
The cloned 26K casein gene was transferred to mouse L-cells and its expression was measured by Northern blot hybridization. When the A clone with 5′- and 3′-flank- ing sequences was transferred, transcripts were detected without glucocorticoid, but in the presence of glucocorticoid, the level of the...
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Published in: | Journal of biochemistry (Tokyo) 1987-01, Vol.101 (1), p.103-110 |
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container_title | Journal of biochemistry (Tokyo) |
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creator | KAWAMURA, Kazuo SATOW, Hiroyasu DO IK, Lee SAKAI, Senkiti TAKADA, Shinji OBINATA, Masuo |
description | The cloned 26K casein gene was transferred to mouse L-cells and its expression was measured by Northern blot hybridization. When the A clone with 5′- and 3′-flank- ing sequences was transferred, transcripts were detected without glucocorticoid, but in the presence of glucocorticoid, the level of the transcripts of heterogeneous sizes increased and their pattern was similar to that observed in the mammary glands of non-lactating mice. When the 6.7 kb Eco fragment containing most of the coding region was transferred, putative precursor and mature mRNAs were detected with out glucocorticoid. Surprisingly, with the addition of glucocorticoid, the level of the transcripts greatly decreased. The presence of multiple sequences responsible for glucocorticoid receptor binding was detected in the 5′-flanking region of the gene in a competition assay using the subfragments of casein gene and on sequence analysis. These results suggest that the 26K casein gene has multiple regulatory domains which interact with glucocorticoid receptors, and these domains may play different roles in the regulation of the casein gene. |
doi_str_mv | 10.1093/oxfordjournals.jbchem.a121880 |
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When the A clone with 5′- and 3′-flank- ing sequences was transferred, transcripts were detected without glucocorticoid, but in the presence of glucocorticoid, the level of the transcripts of heterogeneous sizes increased and their pattern was similar to that observed in the mammary glands of non-lactating mice. When the 6.7 kb Eco fragment containing most of the coding region was transferred, putative precursor and mature mRNAs were detected with out glucocorticoid. Surprisingly, with the addition of glucocorticoid, the level of the transcripts greatly decreased. The presence of multiple sequences responsible for glucocorticoid receptor binding was detected in the 5′-flanking region of the gene in a competition assay using the subfragments of casein gene and on sequence analysis. These results suggest that the 26K casein gene has multiple regulatory domains which interact with glucocorticoid receptors, and these domains may play different roles in the regulation of the casein gene.</description><identifier>ISSN: 0021-924X</identifier><identifier>DOI: 10.1093/oxfordjournals.jbchem.a121880</identifier><identifier>PMID: 3571195</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Animals ; Base Sequence ; casein ; Caseins - genetics ; cloning ; Cloning, Molecular ; gene expression ; Gene Expression Regulation ; Genes ; glucocorticoids ; Glucocorticoids - pharmacology ; L Cells (Cell Line) ; Mice ; Molecular Weight ; Plasmids ; Receptors, Glucocorticoid - biosynthesis ; transduction</subject><ispartof>Journal of biochemistry (Tokyo), 1987-01, Vol.101 (1), p.103-110</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3571195$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KAWAMURA, Kazuo</creatorcontrib><creatorcontrib>SATOW, Hiroyasu</creatorcontrib><creatorcontrib>DO IK, Lee</creatorcontrib><creatorcontrib>SAKAI, Senkiti</creatorcontrib><creatorcontrib>TAKADA, Shinji</creatorcontrib><creatorcontrib>OBINATA, Masuo</creatorcontrib><title>Modulation of the Transferred Mouse 26K Casein Gene in Mouse L Cells by Glucocorticoid Hormone</title><title>Journal of biochemistry (Tokyo)</title><addtitle>J Biochem</addtitle><description>The cloned 26K casein gene was transferred to mouse L-cells and its expression was measured by Northern blot hybridization. When the A clone with 5′- and 3′-flank- ing sequences was transferred, transcripts were detected without glucocorticoid, but in the presence of glucocorticoid, the level of the transcripts of heterogeneous sizes increased and their pattern was similar to that observed in the mammary glands of non-lactating mice. When the 6.7 kb Eco fragment containing most of the coding region was transferred, putative precursor and mature mRNAs were detected with out glucocorticoid. Surprisingly, with the addition of glucocorticoid, the level of the transcripts greatly decreased. The presence of multiple sequences responsible for glucocorticoid receptor binding was detected in the 5′-flanking region of the gene in a competition assay using the subfragments of casein gene and on sequence analysis. These results suggest that the 26K casein gene has multiple regulatory domains which interact with glucocorticoid receptors, and these domains may play different roles in the regulation of the casein gene.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>casein</subject><subject>Caseins - genetics</subject><subject>cloning</subject><subject>Cloning, Molecular</subject><subject>gene expression</subject><subject>Gene Expression Regulation</subject><subject>Genes</subject><subject>glucocorticoids</subject><subject>Glucocorticoids - pharmacology</subject><subject>L Cells (Cell Line)</subject><subject>Mice</subject><subject>Molecular Weight</subject><subject>Plasmids</subject><subject>Receptors, Glucocorticoid - biosynthesis</subject><subject>transduction</subject><issn>0021-924X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNqFkE9Lw0AUxPeg1Fr9CMJe9Ja6f7Kb5ChBU7FFsAWLB8Nu9oWmJtm6m0D77Y20ePXwGB6_YRgGoVtKppQk_N7uS-vM1vauVbWfbnWxgWaqKKNxTM7QmBBGg4SF6wt06f3292Wcj9CIi4jSRIzR58KavlZdZVtsS9xtAK-can0JzoHBC9t7wEy-4FR5qFqcQQt40COY4xTq2mN9wFndF7awrqsKWxk8s66xLVyh83JoBtcnnaDl0-MqnQXz1-w5fZgHFQ_jLoi0FpIQTqQAxrRRTElpVJgwBUJpo4HFajihGACJieKlLE3CYi01TfgE3R1Td85-9-C7vKl8MTRTLQw98ygKY8kl-9dIw2iIE2Iw3pyMvW7A5DtXNcod8tNuAw-OvPId7P-wcl-5jHgk8tn6I3_L-OJdpjRf8h-M-INf</recordid><startdate>198701</startdate><enddate>198701</enddate><creator>KAWAMURA, Kazuo</creator><creator>SATOW, Hiroyasu</creator><creator>DO IK, Lee</creator><creator>SAKAI, Senkiti</creator><creator>TAKADA, Shinji</creator><creator>OBINATA, Masuo</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>198701</creationdate><title>Modulation of the Transferred Mouse 26K Casein Gene in Mouse L Cells by Glucocorticoid Hormone</title><author>KAWAMURA, Kazuo ; SATOW, Hiroyasu ; DO IK, Lee ; SAKAI, Senkiti ; TAKADA, Shinji ; OBINATA, Masuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i348t-7bb56003065e22bda2a66da492ae5abdbe28ae285a2ee080a3f6fd928b6b193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Animals</topic><topic>Base Sequence</topic><topic>casein</topic><topic>Caseins - genetics</topic><topic>cloning</topic><topic>Cloning, Molecular</topic><topic>gene expression</topic><topic>Gene Expression Regulation</topic><topic>Genes</topic><topic>glucocorticoids</topic><topic>Glucocorticoids - pharmacology</topic><topic>L Cells (Cell Line)</topic><topic>Mice</topic><topic>Molecular Weight</topic><topic>Plasmids</topic><topic>Receptors, Glucocorticoid - biosynthesis</topic><topic>transduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KAWAMURA, Kazuo</creatorcontrib><creatorcontrib>SATOW, Hiroyasu</creatorcontrib><creatorcontrib>DO IK, Lee</creatorcontrib><creatorcontrib>SAKAI, Senkiti</creatorcontrib><creatorcontrib>TAKADA, Shinji</creatorcontrib><creatorcontrib>OBINATA, Masuo</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Biotechnology Research Abstracts</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><jtitle>Journal of biochemistry (Tokyo)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KAWAMURA, Kazuo</au><au>SATOW, Hiroyasu</au><au>DO IK, Lee</au><au>SAKAI, Senkiti</au><au>TAKADA, Shinji</au><au>OBINATA, Masuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modulation of the Transferred Mouse 26K Casein Gene in Mouse L Cells by Glucocorticoid Hormone</atitle><jtitle>Journal of biochemistry (Tokyo)</jtitle><addtitle>J Biochem</addtitle><date>1987-01</date><risdate>1987</risdate><volume>101</volume><issue>1</issue><spage>103</spage><epage>110</epage><pages>103-110</pages><issn>0021-924X</issn><abstract>The cloned 26K casein gene was transferred to mouse L-cells and its expression was measured by Northern blot hybridization. When the A clone with 5′- and 3′-flank- ing sequences was transferred, transcripts were detected without glucocorticoid, but in the presence of glucocorticoid, the level of the transcripts of heterogeneous sizes increased and their pattern was similar to that observed in the mammary glands of non-lactating mice. When the 6.7 kb Eco fragment containing most of the coding region was transferred, putative precursor and mature mRNAs were detected with out glucocorticoid. Surprisingly, with the addition of glucocorticoid, the level of the transcripts greatly decreased. The presence of multiple sequences responsible for glucocorticoid receptor binding was detected in the 5′-flanking region of the gene in a competition assay using the subfragments of casein gene and on sequence analysis. These results suggest that the 26K casein gene has multiple regulatory domains which interact with glucocorticoid receptors, and these domains may play different roles in the regulation of the casein gene.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>3571195</pmid><doi>10.1093/oxfordjournals.jbchem.a121880</doi><tpages>8</tpages></addata></record> |
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source | J-STAGE (Japan Science & Technology Information Aggregator, Electronic) - Open Access English articles; Oxford University Press Archive |
subjects | Animals Base Sequence casein Caseins - genetics cloning Cloning, Molecular gene expression Gene Expression Regulation Genes glucocorticoids Glucocorticoids - pharmacology L Cells (Cell Line) Mice Molecular Weight Plasmids Receptors, Glucocorticoid - biosynthesis transduction |
title | Modulation of the Transferred Mouse 26K Casein Gene in Mouse L Cells by Glucocorticoid Hormone |
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