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
Hauptverfasser: I-Cheng Ho, Yang, Li-Hsuan, Morle, Gerald, Leiden, Jeffrey M.
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container_issue 17
container_start_page 6714
container_title Proceedings of the National Academy of Sciences - PNAS
container_volume 86
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.
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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. 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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. 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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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