A T-Cell-Specific Transcriptional Enhancer Element 3′ of Cα in the Human T-Cell Receptor α Locus
A transcriptional enhancer element has been identified 4.5 kilobases 3′ of Cα (constant region α chain) in the human T-cell receptor (TCR) α -chain locus. This enhancer is active on both a TCR Vα (variable region α chain) promoter and the minimal simian virus 40 promoter in TCR α /β Jurkat and EL4 c...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1989-09, Vol.86 (17), p.6714-6718 |
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creator | I-Cheng Ho Yang, Li-Hsuan Morle, Gerald Leiden, Jeffrey M. |
description | A transcriptional enhancer element has been identified 4.5 kilobases 3′ of Cα (constant region α chain) in the human T-cell receptor (TCR) α -chain locus. This enhancer is active on both a TCR Vα (variable region α chain) promoter and the minimal simian virus 40 promoter in TCR α /β Jurkat and EL4 cells but is inactive on a Vα promoter in human TCR γ /δ PEER and Molt-13 cells, clone 13 B cells, and HeLa fibroblasts. The enhancer has been localized to a 116-base-pair BstXI/Dra I restriction enzyme fragment, which lacks immunoglobulin octamer and κ B enhancer motifs but does contain a consensus cAMP-response element (CRE). DNase I footprint analyses demonstrated that the minimal enhancer contains two binding sites for Jurkat nuclear proteins. One of these sites corresponds to the CRE, while the other does not correspond to a known transcriptional enhancer motif. These data support a model in which TCR α gene transcription is regulated by a unique set of cis-acting sequences and trans-acting factors, which are differentially active in cells of the TCR α /β lineage. In addition, the TCR α enhancer may play a role in activating oncogene expression in T-lymphoblastoid tumors that have previously been shown to display chromosomal translocations into the human TCR α locus. |
doi_str_mv | 10.1073/pnas.86.17.6714 |
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This enhancer is active on both a TCR Vα (variable region α chain) promoter and the minimal simian virus 40 promoter in TCR α /β Jurkat and EL4 cells but is inactive on a Vα promoter in human TCR γ /δ PEER and Molt-13 cells, clone 13 B cells, and HeLa fibroblasts. The enhancer has been localized to a 116-base-pair BstXI/Dra I restriction enzyme fragment, which lacks immunoglobulin octamer and κ B enhancer motifs but does contain a consensus cAMP-response element (CRE). DNase I footprint analyses demonstrated that the minimal enhancer contains two binding sites for Jurkat nuclear proteins. One of these sites corresponds to the CRE, while the other does not correspond to a known transcriptional enhancer motif. These data support a model in which TCR α gene transcription is regulated by a unique set of cis-acting sequences and trans-acting factors, which are differentially active in cells of the TCR α /β lineage. In addition, the TCR α enhancer may play a role in activating oncogene expression in T-lymphoblastoid tumors that have previously been shown to display chromosomal translocations into the human TCR α locus.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.86.17.6714</identifier><identifier>PMID: 2788889</identifier><identifier>CODEN: PNASA6</identifier><language>eng</language><publisher>Washington, DC: National Academy of Sciences of the United States of America</publisher><subject>B lymphocytes ; Base Sequence ; Binding sites ; Biological and medical sciences ; Cloning, Molecular ; Enhancer elements ; Enhancer Elements, Genetic ; Fundamental and applied biological sciences. Psychology ; Genes ; Genes, Immunoglobulin ; Genes. Genome ; Genetic loci ; Humans ; Immunoglobulin Constant Regions - genetics ; Immunoglobulin Variable Region - genetics ; Molecular and cellular biology ; Molecular genetics ; Molecular Sequence Data ; Nuclear proteins ; Plasmids ; Receptors, Antigen, T-Cell - genetics ; Restriction Mapping ; T cell antigen receptors ; T lymphocytes ; T-Lymphocytes - immunology ; Transcription, Genetic ; Transfection</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1989-09, Vol.86 (17), p.6714-6718</ispartof><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-cd5f6602cf25d69365f98c7b0b44762a3a0037a416d022180d07c054839a398e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/86/17.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/34605$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/34605$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27903,27904,53769,53771,57995,58228</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19428183$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2788889$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>I-Cheng Ho</creatorcontrib><creatorcontrib>Yang, Li-Hsuan</creatorcontrib><creatorcontrib>Morle, Gerald</creatorcontrib><creatorcontrib>Leiden, Jeffrey M.</creatorcontrib><title>A T-Cell-Specific Transcriptional Enhancer Element 3′ of Cα in the Human T-Cell Receptor α Locus</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>A transcriptional enhancer element has been identified 4.5 kilobases 3′ of Cα (constant region α chain) in the human T-cell receptor (TCR) α -chain locus. This enhancer is active on both a TCR Vα (variable region α chain) promoter and the minimal simian virus 40 promoter in TCR α /β Jurkat and EL4 cells but is inactive on a Vα promoter in human TCR γ /δ PEER and Molt-13 cells, clone 13 B cells, and HeLa fibroblasts. The enhancer has been localized to a 116-base-pair BstXI/Dra I restriction enzyme fragment, which lacks immunoglobulin octamer and κ B enhancer motifs but does contain a consensus cAMP-response element (CRE). DNase I footprint analyses demonstrated that the minimal enhancer contains two binding sites for Jurkat nuclear proteins. One of these sites corresponds to the CRE, while the other does not correspond to a known transcriptional enhancer motif. These data support a model in which TCR α gene transcription is regulated by a unique set of cis-acting sequences and trans-acting factors, which are differentially active in cells of the TCR α /β lineage. In addition, the TCR α enhancer may play a role in activating oncogene expression in T-lymphoblastoid tumors that have previously been shown to display chromosomal translocations into the human TCR α locus.</description><subject>B lymphocytes</subject><subject>Base Sequence</subject><subject>Binding sites</subject><subject>Biological and medical sciences</subject><subject>Cloning, Molecular</subject><subject>Enhancer elements</subject><subject>Enhancer Elements, Genetic</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes</subject><subject>Genes, Immunoglobulin</subject><subject>Genes. Genome</subject><subject>Genetic loci</subject><subject>Humans</subject><subject>Immunoglobulin Constant Regions - genetics</subject><subject>Immunoglobulin Variable Region - genetics</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Sequence Data</subject><subject>Nuclear proteins</subject><subject>Plasmids</subject><subject>Receptors, Antigen, T-Cell - genetics</subject><subject>Restriction Mapping</subject><subject>T cell antigen receptors</subject><subject>T lymphocytes</subject><subject>T-Lymphocytes - immunology</subject><subject>Transcription, Genetic</subject><subject>Transfection</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kb2OEzEUhS0EWsJCjYQEcgNUk73-Gf8UW6yiwCJFQoJQW47HQ7yaP-wZBB2vBA_CQ_AkOMqQhQY3Ls53zr1XB6HHBJYEJLsYOpuWSiyJXApJ-B20IKBJIbiGu2gBQGWhOOX30YOUbgBAlwrO0BmVKj-9QNUV3hYr3zTF-8G7UAeHt9F2ycUwjKHvbIPX3d52zke8bnzruxGzX99-4L7Gq5_fcejwuPf4emptNyfhd975Yewjzvqmd1N6iO7Vtkn-0fyfow-v1tvVdbF5-_rN6mpTOE7ZWLiqrIUA6mpaVkIzUdZaObmDHedSUMssAJOWE1EBpURBBdJByRXTlmnl2Tm6POYO0671lcvLRtuYIYbWxq-mt8H8q3Rhbz72nw3VUhOR_S9mf-w_TT6Npg3J5ZNs5_spmQwpoXSZwYsj6GKfUvT1aQYBc-jFHHoxShgizaGX7Hj692onfi4i689n3SZnmzp34EK6jdWcKqJY5l7O3GHAH_l2kKmnphn9lzGTz_5LZuDJEbhJuawTwbiAkv0Gogi4lQ</recordid><startdate>19890901</startdate><enddate>19890901</enddate><creator>I-Cheng Ho</creator><creator>Yang, Li-Hsuan</creator><creator>Morle, Gerald</creator><creator>Leiden, Jeffrey M.</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19890901</creationdate><title>A T-Cell-Specific Transcriptional Enhancer Element 3′ of Cα in the Human T-Cell Receptor α Locus</title><author>I-Cheng Ho ; Yang, Li-Hsuan ; Morle, Gerald ; Leiden, Jeffrey M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-cd5f6602cf25d69365f98c7b0b44762a3a0037a416d022180d07c054839a398e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>B lymphocytes</topic><topic>Base Sequence</topic><topic>Binding sites</topic><topic>Biological and medical sciences</topic><topic>Cloning, Molecular</topic><topic>Enhancer elements</topic><topic>Enhancer Elements, Genetic</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes</topic><topic>Genes, Immunoglobulin</topic><topic>Genes. Genome</topic><topic>Genetic loci</topic><topic>Humans</topic><topic>Immunoglobulin Constant Regions - genetics</topic><topic>Immunoglobulin Variable Region - genetics</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Sequence Data</topic><topic>Nuclear proteins</topic><topic>Plasmids</topic><topic>Receptors, Antigen, T-Cell - genetics</topic><topic>Restriction Mapping</topic><topic>T cell antigen receptors</topic><topic>T lymphocytes</topic><topic>T-Lymphocytes - immunology</topic><topic>Transcription, Genetic</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>I-Cheng Ho</creatorcontrib><creatorcontrib>Yang, Li-Hsuan</creatorcontrib><creatorcontrib>Morle, Gerald</creatorcontrib><creatorcontrib>Leiden, Jeffrey M.</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><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>I-Cheng Ho</au><au>Yang, Li-Hsuan</au><au>Morle, Gerald</au><au>Leiden, Jeffrey M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A T-Cell-Specific Transcriptional Enhancer Element 3′ of Cα in the Human T-Cell Receptor α Locus</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1989-09-01</date><risdate>1989</risdate><volume>86</volume><issue>17</issue><spage>6714</spage><epage>6718</epage><pages>6714-6718</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><coden>PNASA6</coden><abstract>A transcriptional enhancer element has been identified 4.5 kilobases 3′ of Cα (constant region α chain) in the human T-cell receptor (TCR) α -chain locus. This enhancer is active on both a TCR Vα (variable region α chain) promoter and the minimal simian virus 40 promoter in TCR α /β Jurkat and EL4 cells but is inactive on a Vα promoter in human TCR γ /δ PEER and Molt-13 cells, clone 13 B cells, and HeLa fibroblasts. The enhancer has been localized to a 116-base-pair BstXI/Dra I restriction enzyme fragment, which lacks immunoglobulin octamer and κ B enhancer motifs but does contain a consensus cAMP-response element (CRE). DNase I footprint analyses demonstrated that the minimal enhancer contains two binding sites for Jurkat nuclear proteins. One of these sites corresponds to the CRE, while the other does not correspond to a known transcriptional enhancer motif. These data support a model in which TCR α gene transcription is regulated by a unique set of cis-acting sequences and trans-acting factors, which are differentially active in cells of the TCR α /β lineage. In addition, the TCR α enhancer may play a role in activating oncogene expression in T-lymphoblastoid tumors that have previously been shown to display chromosomal translocations into the human TCR α locus.</abstract><cop>Washington, DC</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>2788889</pmid><doi>10.1073/pnas.86.17.6714</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | B lymphocytes Base Sequence Binding sites Biological and medical sciences Cloning, Molecular Enhancer elements Enhancer Elements, Genetic Fundamental and applied biological sciences. Psychology Genes Genes, Immunoglobulin Genes. Genome Genetic loci Humans Immunoglobulin Constant Regions - genetics Immunoglobulin Variable Region - genetics Molecular and cellular biology Molecular genetics Molecular Sequence Data Nuclear proteins Plasmids Receptors, Antigen, T-Cell - genetics Restriction Mapping T cell antigen receptors T lymphocytes T-Lymphocytes - immunology Transcription, Genetic Transfection |
title | A T-Cell-Specific Transcriptional Enhancer Element 3′ of Cα in the Human T-Cell Receptor α Locus |
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