The same inducible nuclear proteins regulates mitogen activation of both the interleukin-2 receptor-alpha gene and type 1 HIV

Both the interleukin-2 receptor-alpha (Tac, p55, IL-2Rα) gene and the long terminal repeat (LTR) of type 1 HIV are activated by various T cell mitogens. We now demonstrate that an inducible 86 kd nuclear protein termed HIVEN86A specifically binds to both the enhancer element of the HIV-1 LTR and a c...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cell 1988-06, Vol.53 (5), p.827-836
Hauptverfasser: Böhnlein, Ernst, Lowenthal, John W., Siekevitz, Miriam, Ballard, Dean W., Franza, B.Robert, Greene, Warner C.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 836
container_issue 5
container_start_page 827
container_title Cell
container_volume 53
creator Böhnlein, Ernst
Lowenthal, John W.
Siekevitz, Miriam
Ballard, Dean W.
Franza, B.Robert
Greene, Warner C.
description Both the interleukin-2 receptor-alpha (Tac, p55, IL-2Rα) gene and the long terminal repeat (LTR) of type 1 HIV are activated by various T cell mitogens. We now demonstrate that an inducible 86 kd nuclear protein termed HIVEN86A specifically binds to both the enhancer element of the HIV-1 LTR and a closely related 12 bp sequence present in the 5′ regulatory region (−267 to −256) of the IL-2Rα gene. The interaction of these binding sites with HIVEN86A and perhaps other cellular proteins such as NF-κB appears importantly involved in mitogen activation since the isolated IL-2Rα promoter binding site or single elements of the normally duplicated HIV-1 enhancer alone are sufficient to confer mitogen inducibility on an unresponsive heterologous promoter. Together these findings suggest that the normal action of an inducible nuclear DNA binding protein(s) involved in the regulation of IL-2Rα gene expression can be subverted by the HIV-1 provirus to promote activation of retroviral gene transcription.
doi_str_mv 10.1016/0092-8674(88)90099-2
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_78225366</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>0092867488900992</els_id><sourcerecordid>78225366</sourcerecordid><originalsourceid>FETCH-LOGICAL-c386t-df74114847907b5802019e41007d0058018a1bdcb199abc5cbd073bc23cd76753</originalsourceid><addsrcrecordid>eNp9kE1rFTEUhoNY6m3tP1DIQkQXoyeZj2Q2ghRrCwU3tduQSc70RmeSMckUuvC_m-u93GVX4XCe9yXnIeQNg08MWPcZoOeV7ETzQcqPfZn6ir8gGwa9qBom-EuyOSKvyFlKvwBAtm17Sk65rDvo5Ib8vdsiTXpG6rxdjRsmpH41E-pIlxgyOp9oxId10hkTnV0OD-ipNtk96uyCp2GkQ8hbmre7joxxwvW38xUvMYNLDrHS07LVtOSQam9pflqQMnp9c_-anIx6SnhxeM_Jz6tvd5fX1e2P7zeXX28rU8suV3YUDWONbEQPYmglcGA9NgxAWIAyM6nZYM3A-l4PpjWDBVEPhtfGik609Tl5v-8tJ_1ZMWU1u2RwmrTHsCYlJOdt3XUFbPagiSGliKNaopt1fFIM1M662ilVO6VKSvXfuuIl9vbQvw4z2mPooLns3x32Ohk9jVF749IRE50UfQsF-7LHsLh4dBhVMg69QeuKy6xscM__4x_7wp40</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>78225366</pqid></control><display><type>article</type><title>The same inducible nuclear proteins regulates mitogen activation of both the interleukin-2 receptor-alpha gene and type 1 HIV</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Böhnlein, Ernst ; Lowenthal, John W. ; Siekevitz, Miriam ; Ballard, Dean W. ; Franza, B.Robert ; Greene, Warner C.</creator><creatorcontrib>Böhnlein, Ernst ; Lowenthal, John W. ; Siekevitz, Miriam ; Ballard, Dean W. ; Franza, B.Robert ; Greene, Warner C.</creatorcontrib><description>Both the interleukin-2 receptor-alpha (Tac, p55, IL-2Rα) gene and the long terminal repeat (LTR) of type 1 HIV are activated by various T cell mitogens. We now demonstrate that an inducible 86 kd nuclear protein termed HIVEN86A specifically binds to both the enhancer element of the HIV-1 LTR and a closely related 12 bp sequence present in the 5′ regulatory region (−267 to −256) of the IL-2Rα gene. The interaction of these binding sites with HIVEN86A and perhaps other cellular proteins such as NF-κB appears importantly involved in mitogen activation since the isolated IL-2Rα promoter binding site or single elements of the normally duplicated HIV-1 enhancer alone are sufficient to confer mitogen inducibility on an unresponsive heterologous promoter. Together these findings suggest that the normal action of an inducible nuclear DNA binding protein(s) involved in the regulation of IL-2Rα gene expression can be subverted by the HIV-1 provirus to promote activation of retroviral gene transcription.</description><identifier>ISSN: 0092-8674</identifier><identifier>EISSN: 1097-4172</identifier><identifier>DOI: 10.1016/0092-8674(88)90099-2</identifier><identifier>PMID: 2836068</identifier><identifier>CODEN: CELLB5</identifier><language>eng</language><publisher>Cambridge, MA: Elsevier Inc</publisher><subject>AIDS/HIV ; Base Sequence ; Biological and medical sciences ; Cell Line ; DNA Restriction Enzymes ; Enhancer Elements, Genetic ; Fundamental and applied biological sciences. Psychology ; Gene expression ; Gene Expression Regulation - drug effects ; Genes ; Genes, Fungal ; Genes, Regulator ; HIV - genetics ; Interleukin-2 - metabolism ; Mitogens - pharmacology ; Molecular and cellular biology ; Molecular genetics ; Molecular Sequence Data ; Nuclear Proteins - physiology ; Promoter Regions, Genetic ; Receptors, Immunologic - genetics ; Receptors, Interleukin-2 ; Sequence Homology, Nucleic Acid</subject><ispartof>Cell, 1988-06, Vol.53 (5), p.827-836</ispartof><rights>1988</rights><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-df74114847907b5802019e41007d0058018a1bdcb199abc5cbd073bc23cd76753</citedby><cites>FETCH-LOGICAL-c386t-df74114847907b5802019e41007d0058018a1bdcb199abc5cbd073bc23cd76753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0092-8674(88)90099-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=7687950$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2836068$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Böhnlein, Ernst</creatorcontrib><creatorcontrib>Lowenthal, John W.</creatorcontrib><creatorcontrib>Siekevitz, Miriam</creatorcontrib><creatorcontrib>Ballard, Dean W.</creatorcontrib><creatorcontrib>Franza, B.Robert</creatorcontrib><creatorcontrib>Greene, Warner C.</creatorcontrib><title>The same inducible nuclear proteins regulates mitogen activation of both the interleukin-2 receptor-alpha gene and type 1 HIV</title><title>Cell</title><addtitle>Cell</addtitle><description>Both the interleukin-2 receptor-alpha (Tac, p55, IL-2Rα) gene and the long terminal repeat (LTR) of type 1 HIV are activated by various T cell mitogens. We now demonstrate that an inducible 86 kd nuclear protein termed HIVEN86A specifically binds to both the enhancer element of the HIV-1 LTR and a closely related 12 bp sequence present in the 5′ regulatory region (−267 to −256) of the IL-2Rα gene. The interaction of these binding sites with HIVEN86A and perhaps other cellular proteins such as NF-κB appears importantly involved in mitogen activation since the isolated IL-2Rα promoter binding site or single elements of the normally duplicated HIV-1 enhancer alone are sufficient to confer mitogen inducibility on an unresponsive heterologous promoter. Together these findings suggest that the normal action of an inducible nuclear DNA binding protein(s) involved in the regulation of IL-2Rα gene expression can be subverted by the HIV-1 provirus to promote activation of retroviral gene transcription.</description><subject>AIDS/HIV</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>DNA Restriction Enzymes</subject><subject>Enhancer Elements, Genetic</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Genes</subject><subject>Genes, Fungal</subject><subject>Genes, Regulator</subject><subject>HIV - genetics</subject><subject>Interleukin-2 - metabolism</subject><subject>Mitogens - pharmacology</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Sequence Data</subject><subject>Nuclear Proteins - physiology</subject><subject>Promoter Regions, Genetic</subject><subject>Receptors, Immunologic - genetics</subject><subject>Receptors, Interleukin-2</subject><subject>Sequence Homology, Nucleic Acid</subject><issn>0092-8674</issn><issn>1097-4172</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1rFTEUhoNY6m3tP1DIQkQXoyeZj2Q2ghRrCwU3tduQSc70RmeSMckUuvC_m-u93GVX4XCe9yXnIeQNg08MWPcZoOeV7ETzQcqPfZn6ir8gGwa9qBom-EuyOSKvyFlKvwBAtm17Sk65rDvo5Ib8vdsiTXpG6rxdjRsmpH41E-pIlxgyOp9oxId10hkTnV0OD-ipNtk96uyCp2GkQ8hbmre7joxxwvW38xUvMYNLDrHS07LVtOSQam9pflqQMnp9c_-anIx6SnhxeM_Jz6tvd5fX1e2P7zeXX28rU8suV3YUDWONbEQPYmglcGA9NgxAWIAyM6nZYM3A-l4PpjWDBVEPhtfGik609Tl5v-8tJ_1ZMWU1u2RwmrTHsCYlJOdt3XUFbPagiSGliKNaopt1fFIM1M662ilVO6VKSvXfuuIl9vbQvw4z2mPooLns3x32Ohk9jVF749IRE50UfQsF-7LHsLh4dBhVMg69QeuKy6xscM__4x_7wp40</recordid><startdate>19880603</startdate><enddate>19880603</enddate><creator>Böhnlein, Ernst</creator><creator>Lowenthal, John W.</creator><creator>Siekevitz, Miriam</creator><creator>Ballard, Dean W.</creator><creator>Franza, B.Robert</creator><creator>Greene, Warner C.</creator><general>Elsevier Inc</general><general>Cell Press</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>7X8</scope></search><sort><creationdate>19880603</creationdate><title>The same inducible nuclear proteins regulates mitogen activation of both the interleukin-2 receptor-alpha gene and type 1 HIV</title><author>Böhnlein, Ernst ; Lowenthal, John W. ; Siekevitz, Miriam ; Ballard, Dean W. ; Franza, B.Robert ; Greene, Warner C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-df74114847907b5802019e41007d0058018a1bdcb199abc5cbd073bc23cd76753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>AIDS/HIV</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>DNA Restriction Enzymes</topic><topic>Enhancer Elements, Genetic</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene expression</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Genes</topic><topic>Genes, Fungal</topic><topic>Genes, Regulator</topic><topic>HIV - genetics</topic><topic>Interleukin-2 - metabolism</topic><topic>Mitogens - pharmacology</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Sequence Data</topic><topic>Nuclear Proteins - physiology</topic><topic>Promoter Regions, Genetic</topic><topic>Receptors, Immunologic - genetics</topic><topic>Receptors, Interleukin-2</topic><topic>Sequence Homology, Nucleic Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Böhnlein, Ernst</creatorcontrib><creatorcontrib>Lowenthal, John W.</creatorcontrib><creatorcontrib>Siekevitz, Miriam</creatorcontrib><creatorcontrib>Ballard, Dean W.</creatorcontrib><creatorcontrib>Franza, B.Robert</creatorcontrib><creatorcontrib>Greene, Warner C.</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>MEDLINE - Academic</collection><jtitle>Cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Böhnlein, Ernst</au><au>Lowenthal, John W.</au><au>Siekevitz, Miriam</au><au>Ballard, Dean W.</au><au>Franza, B.Robert</au><au>Greene, Warner C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The same inducible nuclear proteins regulates mitogen activation of both the interleukin-2 receptor-alpha gene and type 1 HIV</atitle><jtitle>Cell</jtitle><addtitle>Cell</addtitle><date>1988-06-03</date><risdate>1988</risdate><volume>53</volume><issue>5</issue><spage>827</spage><epage>836</epage><pages>827-836</pages><issn>0092-8674</issn><eissn>1097-4172</eissn><coden>CELLB5</coden><abstract>Both the interleukin-2 receptor-alpha (Tac, p55, IL-2Rα) gene and the long terminal repeat (LTR) of type 1 HIV are activated by various T cell mitogens. We now demonstrate that an inducible 86 kd nuclear protein termed HIVEN86A specifically binds to both the enhancer element of the HIV-1 LTR and a closely related 12 bp sequence present in the 5′ regulatory region (−267 to −256) of the IL-2Rα gene. The interaction of these binding sites with HIVEN86A and perhaps other cellular proteins such as NF-κB appears importantly involved in mitogen activation since the isolated IL-2Rα promoter binding site or single elements of the normally duplicated HIV-1 enhancer alone are sufficient to confer mitogen inducibility on an unresponsive heterologous promoter. Together these findings suggest that the normal action of an inducible nuclear DNA binding protein(s) involved in the regulation of IL-2Rα gene expression can be subverted by the HIV-1 provirus to promote activation of retroviral gene transcription.</abstract><cop>Cambridge, MA</cop><pub>Elsevier Inc</pub><pmid>2836068</pmid><doi>10.1016/0092-8674(88)90099-2</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0092-8674
ispartof Cell, 1988-06, Vol.53 (5), p.827-836
issn 0092-8674
1097-4172
language eng
recordid cdi_proquest_miscellaneous_78225366
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects AIDS/HIV
Base Sequence
Biological and medical sciences
Cell Line
DNA Restriction Enzymes
Enhancer Elements, Genetic
Fundamental and applied biological sciences. Psychology
Gene expression
Gene Expression Regulation - drug effects
Genes
Genes, Fungal
Genes, Regulator
HIV - genetics
Interleukin-2 - metabolism
Mitogens - pharmacology
Molecular and cellular biology
Molecular genetics
Molecular Sequence Data
Nuclear Proteins - physiology
Promoter Regions, Genetic
Receptors, Immunologic - genetics
Receptors, Interleukin-2
Sequence Homology, Nucleic Acid
title The same inducible nuclear proteins regulates mitogen activation of both the interleukin-2 receptor-alpha gene and type 1 HIV
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T22%3A25%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20same%20inducible%20nuclear%20proteins%20regulates%20mitogen%20activation%20of%20both%20the%20interleukin-2%20receptor-alpha%20gene%20and%20type%201%20HIV&rft.jtitle=Cell&rft.au=B%C3%B6hnlein,%20Ernst&rft.date=1988-06-03&rft.volume=53&rft.issue=5&rft.spage=827&rft.epage=836&rft.pages=827-836&rft.issn=0092-8674&rft.eissn=1097-4172&rft.coden=CELLB5&rft_id=info:doi/10.1016/0092-8674(88)90099-2&rft_dat=%3Cproquest_cross%3E78225366%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=78225366&rft_id=info:pmid/2836068&rft_els_id=0092867488900992&rfr_iscdi=true