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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
13
pubmed:dateCreated
2005-6-20
pubmed:abstractText
Transcriptional activation by Gcn4p is dependent on the coactivators SWI/SNF, SAGA, and Srb Mediator, which are recruited by Gcn4p and stimulate assembly of the pre-initiation complex (PIC) at the ARG1 promoter in vivo. We show that recruitment of all three coactivators is nearly simultaneous with binding of Gcn4p at ARG1 and is followed quickly by PIC formation and elongation by RNA polymerase II (Pol II) through the open reading frame. Despite the simultaneous recruitment of coactivators, rapid recruitment of SWI/SNF depends on the histone acetyltransferase (HAT) subunit of SAGA (Gcn5p), a non-HAT function of SAGA, and on Mediator. SAGA recruitment in turn is strongly stimulated by Mediator and the RSC complex. Recruitment of Mediator, by contrast, occurs independently of the other coactivators at ARG1. We confirm the roles of Mediator and SAGA in TATA binding protein (TBP) recruitment and demonstrate that all four coactivators under study enhance Pol II recruitment or promoter clearance following TBP binding. We also present evidence that SWI/SNF and SAGA stimulate transcription elongation downstream from the promoter. These functions can be limited to discrete time intervals, providing evidence for multiple stages in the induction process. Our findings reveal a program of coactivator recruitment and PIC assembly that distinguishes Gcn4p from other yeast activators studied thus far.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-10082564, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-10319811, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-10376604, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-10376605, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-10549298, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-10619019, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-10638745, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-10746732, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-10817999, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-10913179, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-10966474, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-11007477, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-11018011, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-11089979, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-11485988, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-11485989, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-11562354, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-12101232, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-12419247, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-12432091, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-12482986, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-12600943, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-12665580, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-12769853, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-12782657, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-14585989, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-14612422, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-14685262, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-14871930, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-15121833, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-15359273, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-15385957, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-15457216, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-15632065, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-15831453, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-1618865, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-1628834, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-3045517, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-8628270, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-8887556, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-9224714, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-9488488, http://linkedlifedata.com/resource/pubmed/commentcorrection/15964818-9697775
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Acetyltransferases, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Histone Acetyltransferases, http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Protein Subunits, http://linkedlifedata.com/resource/pubmed/chemical/RNA Polymerase II, http://linkedlifedata.com/resource/pubmed/chemical/RSC complex, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/Saccharomyces cerevisiae Proteins, http://linkedlifedata.com/resource/pubmed/chemical/TATA-Binding Protein Associated..., http://linkedlifedata.com/resource/pubmed/chemical/TATA-Box Binding Protein, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0270-7306
pubmed:author
pubmed:issnType
Print
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5626-38
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:15964818-Mutation, pubmed-meshheading:15964818-Saccharomyces cerevisiae, pubmed-meshheading:15964818-Kinetics, pubmed-meshheading:15964818-Saccharomyces cerevisiae Proteins, pubmed-meshheading:15964818-Protein Subunits, pubmed-meshheading:15964818-Cells, Cultured, pubmed-meshheading:15964818-Models, Biological, pubmed-meshheading:15964818-Transcription, Genetic, pubmed-meshheading:15964818-Acetyltransferases, pubmed-meshheading:15964818-Protein Kinases, pubmed-meshheading:15964818-Promoter Regions, Genetic, pubmed-meshheading:15964818-DNA-Binding Proteins, pubmed-meshheading:15964818-RNA Polymerase II, pubmed-meshheading:15964818-Sequence Deletion, pubmed-meshheading:15964818-Transcriptional Activation, pubmed-meshheading:15964818-Transcription Factors, pubmed-meshheading:15964818-Gene Expression Regulation, Fungal, pubmed-meshheading:15964818-Histone Acetyltransferases
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