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TFIID sequence recognition of the initiator and sequences farther downstream in Drosophila class II genes
Immunopurified TFIID produces a large DNase I footprint over the hsp70, hsp26, and histone H3 promoters of Drosophila. These footprints span from the TATA element to a position approximately 35 nucleotides downstream from the transcription start site. Using a "missing nucleoside" analysis,...
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Published in: | Genes & development 1994-04, Vol.8 (7), p.830-842 |
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description | Immunopurified TFIID produces a large DNase I footprint over the hsp70, hsp26, and histone H3 promoters of Drosophila. These footprints span from the TATA element to a position approximately 35 nucleotides downstream from the transcription start site. Using a "missing nucleoside" analysis, four regions within the three promoters have been found to be important for TFIID binding: the TATA element, the initiator, and two regions located approximately 18 and 28 nucleotides downstream of the transcription start site. On the basis of the missing nucleoside data, the initiator appears to contribute as much to the affinity as the TATA element. However, there is weak conservation of the sequence in this region. To determine whether a preferred binding sequence exists in the vicinity of the initiator, the nucleotide composition of this region within the hsp70 promoter was randomized and then subjected to selection by TFIID. After five rounds of selection, the preferred sequence motif--G/A/T C/TAT/GTG--emerged. This motif is a close match to consensus sequences that have been derived by comparing the initiator region of numerous insect promoters. Selection of this sequence demonstrates that sequence-specific interactions downstream of the TATA element contribute to the interaction of TFIID on a wide spectrum of promoters. |
doi_str_mv | 10.1101/gad.8.7.830 |
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A ; EMANUEL, P. A ; GILMOUR, D. S</creator><creatorcontrib>PURNELL, B. A ; EMANUEL, P. A ; GILMOUR, D. S</creatorcontrib><description>Immunopurified TFIID produces a large DNase I footprint over the hsp70, hsp26, and histone H3 promoters of Drosophila. These footprints span from the TATA element to a position approximately 35 nucleotides downstream from the transcription start site. Using a "missing nucleoside" analysis, four regions within the three promoters have been found to be important for TFIID binding: the TATA element, the initiator, and two regions located approximately 18 and 28 nucleotides downstream of the transcription start site. On the basis of the missing nucleoside data, the initiator appears to contribute as much to the affinity as the TATA element. However, there is weak conservation of the sequence in this region. To determine whether a preferred binding sequence exists in the vicinity of the initiator, the nucleotide composition of this region within the hsp70 promoter was randomized and then subjected to selection by TFIID. After five rounds of selection, the preferred sequence motif--G/A/T C/TAT/GTG--emerged. This motif is a close match to consensus sequences that have been derived by comparing the initiator region of numerous insect promoters. Selection of this sequence demonstrates that sequence-specific interactions downstream of the TATA element contribute to the interaction of TFIID on a wide spectrum of promoters.</description><identifier>ISSN: 0890-9369</identifier><identifier>EISSN: 1549-5477</identifier><identifier>DOI: 10.1101/gad.8.7.830</identifier><identifier>PMID: 7926771</identifier><identifier>CODEN: GEDEEP</identifier><language>eng</language><publisher>Cold Spring Harbor, NY: Cold Spring Harbor Laboratory</publisher><subject>Animals ; Base Sequence ; Binding Sites ; Biological and medical sciences ; Consensus Sequence - genetics ; DNA - metabolism ; Drosophila ; Drosophila - genetics ; Drosophila Proteins ; Fundamental and applied biological sciences. Psychology ; Genes, Insect - genetics ; Heat-Shock Proteins - genetics ; Histones - genetics ; HSP70 Heat-Shock Proteins - genetics ; Molecular and cellular biology ; Molecular genetics ; Molecular Sequence Data ; Promoter Regions, Genetic - genetics ; Sequence Analysis, DNA ; TATA Box - genetics ; Transcription Factor TFIID ; Transcription Factors - isolation & purification ; Transcription Factors - metabolism ; Transcription, Genetic ; Transcription. Transcription factor. Splicing. 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A</creatorcontrib><creatorcontrib>EMANUEL, P. A</creatorcontrib><creatorcontrib>GILMOUR, D. S</creatorcontrib><title>TFIID sequence recognition of the initiator and sequences farther downstream in Drosophila class II genes</title><title>Genes & development</title><addtitle>Genes Dev</addtitle><description>Immunopurified TFIID produces a large DNase I footprint over the hsp70, hsp26, and histone H3 promoters of Drosophila. These footprints span from the TATA element to a position approximately 35 nucleotides downstream from the transcription start site. Using a "missing nucleoside" analysis, four regions within the three promoters have been found to be important for TFIID binding: the TATA element, the initiator, and two regions located approximately 18 and 28 nucleotides downstream of the transcription start site. On the basis of the missing nucleoside data, the initiator appears to contribute as much to the affinity as the TATA element. However, there is weak conservation of the sequence in this region. To determine whether a preferred binding sequence exists in the vicinity of the initiator, the nucleotide composition of this region within the hsp70 promoter was randomized and then subjected to selection by TFIID. After five rounds of selection, the preferred sequence motif--G/A/T C/TAT/GTG--emerged. This motif is a close match to consensus sequences that have been derived by comparing the initiator region of numerous insect promoters. Selection of this sequence demonstrates that sequence-specific interactions downstream of the TATA element contribute to the interaction of TFIID on a wide spectrum of promoters.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Binding Sites</subject><subject>Biological and medical sciences</subject><subject>Consensus Sequence - genetics</subject><subject>DNA - metabolism</subject><subject>Drosophila</subject><subject>Drosophila - genetics</subject><subject>Drosophila Proteins</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes, Insect - genetics</subject><subject>Heat-Shock Proteins - genetics</subject><subject>Histones - genetics</subject><subject>HSP70 Heat-Shock Proteins - genetics</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Sequence Data</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Sequence Analysis, DNA</subject><subject>TATA Box - genetics</subject><subject>Transcription Factor TFIID</subject><subject>Transcription Factors - isolation & purification</subject><subject>Transcription Factors - metabolism</subject><subject>Transcription, Genetic</subject><subject>Transcription. Transcription factor. Splicing. 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S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-45f1fc84537470f7590e6471b31242b39f3ccc769fe8fd0c4d530aac3cce2e783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Base Sequence</topic><topic>Binding Sites</topic><topic>Biological and medical sciences</topic><topic>Consensus Sequence - genetics</topic><topic>DNA - metabolism</topic><topic>Drosophila</topic><topic>Drosophila - genetics</topic><topic>Drosophila Proteins</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes, Insect - genetics</topic><topic>Heat-Shock Proteins - genetics</topic><topic>Histones - genetics</topic><topic>HSP70 Heat-Shock Proteins - genetics</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Sequence Data</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Sequence Analysis, DNA</topic><topic>TATA Box - genetics</topic><topic>Transcription Factor TFIID</topic><topic>Transcription Factors - isolation & purification</topic><topic>Transcription Factors - metabolism</topic><topic>Transcription, Genetic</topic><topic>Transcription. Transcription factor. Splicing. Rna processing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PURNELL, B. A</creatorcontrib><creatorcontrib>EMANUEL, P. A</creatorcontrib><creatorcontrib>GILMOUR, D. 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S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>TFIID sequence recognition of the initiator and sequences farther downstream in Drosophila class II genes</atitle><jtitle>Genes & development</jtitle><addtitle>Genes Dev</addtitle><date>1994-04-01</date><risdate>1994</risdate><volume>8</volume><issue>7</issue><spage>830</spage><epage>842</epage><pages>830-842</pages><issn>0890-9369</issn><eissn>1549-5477</eissn><coden>GEDEEP</coden><abstract>Immunopurified TFIID produces a large DNase I footprint over the hsp70, hsp26, and histone H3 promoters of Drosophila. These footprints span from the TATA element to a position approximately 35 nucleotides downstream from the transcription start site. Using a "missing nucleoside" analysis, four regions within the three promoters have been found to be important for TFIID binding: the TATA element, the initiator, and two regions located approximately 18 and 28 nucleotides downstream of the transcription start site. On the basis of the missing nucleoside data, the initiator appears to contribute as much to the affinity as the TATA element. However, there is weak conservation of the sequence in this region. To determine whether a preferred binding sequence exists in the vicinity of the initiator, the nucleotide composition of this region within the hsp70 promoter was randomized and then subjected to selection by TFIID. After five rounds of selection, the preferred sequence motif--G/A/T C/TAT/GTG--emerged. This motif is a close match to consensus sequences that have been derived by comparing the initiator region of numerous insect promoters. Selection of this sequence demonstrates that sequence-specific interactions downstream of the TATA element contribute to the interaction of TFIID on a wide spectrum of promoters.</abstract><cop>Cold Spring Harbor, NY</cop><pub>Cold Spring Harbor Laboratory</pub><pmid>7926771</pmid><doi>10.1101/gad.8.7.830</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Base Sequence Binding Sites Biological and medical sciences Consensus Sequence - genetics DNA - metabolism Drosophila Drosophila - genetics Drosophila Proteins Fundamental and applied biological sciences. Psychology Genes, Insect - genetics Heat-Shock Proteins - genetics Histones - genetics HSP70 Heat-Shock Proteins - genetics Molecular and cellular biology Molecular genetics Molecular Sequence Data Promoter Regions, Genetic - genetics Sequence Analysis, DNA TATA Box - genetics Transcription Factor TFIID Transcription Factors - isolation & purification Transcription Factors - metabolism Transcription, Genetic Transcription. Transcription factor. Splicing. Rna processing |
title | TFIID sequence recognition of the initiator and sequences farther downstream in Drosophila class II genes |
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