Targeting TBP to a non-TATA box cis-regulatory element : a TBP-containing complex activates transcription from snRNA promoters through the PSE
In the human small nuclear RNA (snRNA) promoters, the presence of a TATA box recognized by the TATA box-binding protein (TBP) determines the selection of RNA polymerase III over RNA polymerase II. The RNA polymerase II snRNA promoters are, therefore, good candidates for TBP-independent promoters. We...
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Veröffentlicht in: | Genes & development 1993-08, Vol.7 (8), p.1535-1548 |
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description | In the human small nuclear RNA (snRNA) promoters, the presence of a TATA box recognized by the TATA box-binding protein (TBP) determines the selection of RNA polymerase III over RNA polymerase II. The RNA polymerase II snRNA promoters are, therefore, good candidates for TBP-independent promoters. We show here, however, that TBP activates transcription from RNA polymerase II snRNA promoters through a non-TATA box element, the snRNA proximal sequence element (PSE), as part of a new snRNA-activating protein complex (SNAPc). In contrast to the previously identified TBP-containing complexes SL1, TFIID, and TFIIIB, which appear dedicated to transcription by a single RNA polymerase, SNAPc is also essential for RNA polymerase III transcription from the U6 snRNA promoter. The U6 initiation complex appears to contain two forms of TBP, one bound to the TATA box and one bound to the PSE as a part of SNAPc, suggesting that multiple TBP molecules can have different functions within a single promoter. |
doi_str_mv | 10.1101/gad.7.8.1535 |
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L</creatorcontrib><creatorcontrib>HENRY, R. W</creatorcontrib><creatorcontrib>HERNANDEZ, N</creatorcontrib><title>Targeting TBP to a non-TATA box cis-regulatory element : a TBP-containing complex activates transcription from snRNA promoters through the PSE</title><title>Genes & development</title><addtitle>Genes Dev</addtitle><description>In the human small nuclear RNA (snRNA) promoters, the presence of a TATA box recognized by the TATA box-binding protein (TBP) determines the selection of RNA polymerase III over RNA polymerase II. The RNA polymerase II snRNA promoters are, therefore, good candidates for TBP-independent promoters. We show here, however, that TBP activates transcription from RNA polymerase II snRNA promoters through a non-TATA box element, the snRNA proximal sequence element (PSE), as part of a new snRNA-activating protein complex (SNAPc). In contrast to the previously identified TBP-containing complexes SL1, TFIID, and TFIIIB, which appear dedicated to transcription by a single RNA polymerase, SNAPc is also essential for RNA polymerase III transcription from the U6 snRNA promoter. The U6 initiation complex appears to contain two forms of TBP, one bound to the TATA box and one bound to the PSE as a part of SNAPc, suggesting that multiple TBP molecules can have different functions within a single promoter.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Cross-Linking Reagents</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>DNA-Directed RNA Polymerases - biosynthesis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Mice</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Sequence Data</subject><subject>Promoter Regions, Genetic</subject><subject>Proteins</subject><subject>Ribonucleoprotein, U4-U6 Small Nuclear - genetics</subject><subject>RNA Polymerase II - biosynthesis</subject><subject>RNA Polymerase III - biosynthesis</subject><subject>Structure-Activity Relationship</subject><subject>TATA Box</subject><subject>TATA-Box Binding Protein</subject><subject>Trans-Activators - metabolism</subject><subject>Transcription Factors - metabolism</subject><subject>Transcription. Transcription factor. Splicing. Rna processing</subject><subject>Transcriptional Activation</subject><issn>0890-9369</issn><issn>1549-5477</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EKkvhxhXJB9QT2fojdmJuS1U-pKpUEM6W7UzSoMRebKdq_wS_Ga-66pXTO9I8MxrNg9BbSraUEno-mn7bbNstFVw8QxsqalWJummeow1pFakUl-olepXSb0KIJFKeoJOWc6U43aC_nYkj5MmPuPt0g3PABvvgq27X7bAN99hNqYowrrPJIT5gmGEBn_HHwpWBygWfzeQP8y4s-xnusXF5ujMZEs7R-OTitM9T8HiIYcHJ_7je4X0pQ4ZYkNsY1vG2JOCbn5ev0YvBzAneHPMU_fp82V18ra6-f_l2sbuqXC1IroQF66wcHB96xQzrVW2ZZTVvnCPKSU6ctYII0g-9Y1ZSI40RTNKeCWtb4Kfo7HFvueTPCinrZUoO5tl4CGvSjWgbymT7X5BKJRQXrIAfHkEXQ0oRBr2P02Lig6ZEHzzp4kk3utUHTwV_d9y72gX6J_gopvTfH_smOTMP5ZPFxBNWtzUX5bx_bRyc6A</recordid><startdate>19930801</startdate><enddate>19930801</enddate><creator>SADOWSKI, C. L</creator><creator>HENRY, R. 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W ; HERNANDEZ, N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-5bebcb6fc3fd92a2d94b2b2437cc09c630cbb5050dfdc2b61a6aa5261d25bb8e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Cross-Linking Reagents</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>DNA-Directed RNA Polymerases - biosynthesis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Mice</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Sequence Data</topic><topic>Promoter Regions, Genetic</topic><topic>Proteins</topic><topic>Ribonucleoprotein, U4-U6 Small Nuclear - genetics</topic><topic>RNA Polymerase II - biosynthesis</topic><topic>RNA Polymerase III - biosynthesis</topic><topic>Structure-Activity Relationship</topic><topic>TATA Box</topic><topic>TATA-Box Binding Protein</topic><topic>Trans-Activators - metabolism</topic><topic>Transcription Factors - metabolism</topic><topic>Transcription. Transcription factor. Splicing. Rna processing</topic><topic>Transcriptional Activation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SADOWSKI, C. L</creatorcontrib><creatorcontrib>HENRY, R. W</creatorcontrib><creatorcontrib>HERNANDEZ, N</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>MEDLINE - Academic</collection><jtitle>Genes & development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SADOWSKI, C. L</au><au>HENRY, R. W</au><au>HERNANDEZ, N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeting TBP to a non-TATA box cis-regulatory element : a TBP-containing complex activates transcription from snRNA promoters through the PSE</atitle><jtitle>Genes & development</jtitle><addtitle>Genes Dev</addtitle><date>1993-08-01</date><risdate>1993</risdate><volume>7</volume><issue>8</issue><spage>1535</spage><epage>1548</epage><pages>1535-1548</pages><issn>0890-9369</issn><eissn>1549-5477</eissn><coden>GEDEEP</coden><abstract>In the human small nuclear RNA (snRNA) promoters, the presence of a TATA box recognized by the TATA box-binding protein (TBP) determines the selection of RNA polymerase III over RNA polymerase II. The RNA polymerase II snRNA promoters are, therefore, good candidates for TBP-independent promoters. We show here, however, that TBP activates transcription from RNA polymerase II snRNA promoters through a non-TATA box element, the snRNA proximal sequence element (PSE), as part of a new snRNA-activating protein complex (SNAPc). In contrast to the previously identified TBP-containing complexes SL1, TFIID, and TFIIIB, which appear dedicated to transcription by a single RNA polymerase, SNAPc is also essential for RNA polymerase III transcription from the U6 snRNA promoter. The U6 initiation complex appears to contain two forms of TBP, one bound to the TATA box and one bound to the PSE as a part of SNAPc, suggesting that multiple TBP molecules can have different functions within a single promoter.</abstract><cop>Cold Spring Harbor, NY</cop><pub>Cold Spring Harbor Laboratory</pub><pmid>8339931</pmid><doi>10.1101/gad.7.8.1535</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Base Sequence Biological and medical sciences Cross-Linking Reagents DNA-Binding Proteins - metabolism DNA-Directed RNA Polymerases - biosynthesis Fundamental and applied biological sciences. Psychology Humans Mice Molecular and cellular biology Molecular genetics Molecular Sequence Data Promoter Regions, Genetic Proteins Ribonucleoprotein, U4-U6 Small Nuclear - genetics RNA Polymerase II - biosynthesis RNA Polymerase III - biosynthesis Structure-Activity Relationship TATA Box TATA-Box Binding Protein Trans-Activators - metabolism Transcription Factors - metabolism Transcription. Transcription factor. Splicing. Rna processing Transcriptional Activation |
title | Targeting TBP to a non-TATA box cis-regulatory element : a TBP-containing complex activates transcription from snRNA promoters through the PSE |
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