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Article: Holo-TFIID supports transcriptional stimulation by diverse activators and from a TATA-less promoter

TitleHolo-TFIID supports transcriptional stimulation by diverse activators and from a TATA-less promoter
Authors
KeywordsTATA box
TATA-less promoter
TFIID
Transcriptional activation
Issue Date1992
Citation
Genes and Development, 1992, v. 6, n. 10, p. 1964-1974 How to Cite?
AbstractTranscription factor HD (TFIID) binds to TATA boxes, nucleating the assembly of initiation complexes containing several general transcription factors and RNA polymerase II. Recently, TFIID was shown to be a multisubunit complex containing a TATA box-binding polypeptide (TBF) and several tightly associated polypeptides (TAFs), which are required for transcriptional stimulation by activator proteins. Here, we report the development of a human cell line expressing an epitope-tagged TBP and the immunopurification of a native, high-molecular-weight form of TFIID that supports transcriptional stimulation by several different classes of activation domains. Recovery of basal and activated TFIID transcriptional specific activity was close to ∼100%. Electrophoretic mobility-shift analysis demonstrated a single major DNA-protein complex. This holo-TFIID contains TAFs of -250, 125, 95, 78, and 50 kD and sediments at 17S. Holo-TFIID produced an extended footprint over the adenovirus major late promoter TATA box and initiator sequence and supported transcriptional activation from a promoter lacking a TATA box. These results lead us to hypothesize that a single multisubunit TFIID protein supports transcriptional stimulation by diverse activation domains and from a TATA-less promoter.
Persistent Identifierhttp://hdl.handle.net/10722/325600
ISSN
2023 Impact Factor: 7.5
2023 SCImago Journal Rankings: 5.015
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhou, Qiang-
dc.contributor.authorLieberman, Paul M.-
dc.contributor.authorBoyer, Thomas G.-
dc.contributor.authorBerk, Arnold J.-
dc.date.accessioned2023-02-27T07:34:40Z-
dc.date.available2023-02-27T07:34:40Z-
dc.date.issued1992-
dc.identifier.citationGenes and Development, 1992, v. 6, n. 10, p. 1964-1974-
dc.identifier.issn0890-9369-
dc.identifier.urihttp://hdl.handle.net/10722/325600-
dc.description.abstractTranscription factor HD (TFIID) binds to TATA boxes, nucleating the assembly of initiation complexes containing several general transcription factors and RNA polymerase II. Recently, TFIID was shown to be a multisubunit complex containing a TATA box-binding polypeptide (TBF) and several tightly associated polypeptides (TAFs), which are required for transcriptional stimulation by activator proteins. Here, we report the development of a human cell line expressing an epitope-tagged TBP and the immunopurification of a native, high-molecular-weight form of TFIID that supports transcriptional stimulation by several different classes of activation domains. Recovery of basal and activated TFIID transcriptional specific activity was close to ∼100%. Electrophoretic mobility-shift analysis demonstrated a single major DNA-protein complex. This holo-TFIID contains TAFs of -250, 125, 95, 78, and 50 kD and sediments at 17S. Holo-TFIID produced an extended footprint over the adenovirus major late promoter TATA box and initiator sequence and supported transcriptional activation from a promoter lacking a TATA box. These results lead us to hypothesize that a single multisubunit TFIID protein supports transcriptional stimulation by diverse activation domains and from a TATA-less promoter.-
dc.languageeng-
dc.relation.ispartofGenes and Development-
dc.subjectTATA box-
dc.subjectTATA-less promoter-
dc.subjectTFIID-
dc.subjectTranscriptional activation-
dc.titleHolo-TFIID supports transcriptional stimulation by diverse activators and from a TATA-less promoter-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1101/gad.6.10.1964-
dc.identifier.pmid1398073-
dc.identifier.scopuseid_2-s2.0-0026726131-
dc.identifier.volume6-
dc.identifier.issue10-
dc.identifier.spage1964-
dc.identifier.epage1974-
dc.identifier.isiWOS:A1992JT97900013-

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