An array of coactivators is required for optimal recruitment of TATA binding protein and RNA polymerase II by promoter-bound Gcn4p.
about
Activator Gcn4 employs multiple segments of Med15/Gal11, including the KIX domain, to recruit mediator to target genes in vivoMinimal components of the RNA polymerase II transcription apparatus determine the consensus TATA boxComposition of the SAGA complex in plants and its role in controlling gene expression in response to abiotic stressesCcr4-Not complex: the control freak of eukaryotic cellsSgf29p facilitates the recruitment of TATA box binding protein but does not alter SAGA's global structural integrity in vivo.Mediator complex association with constitutively transcribed genes in yeastVps factors are required for efficient transcription elongation in budding yeast.Mcm1p binding sites in ARG1 positively regulate Gcn4p binding and SWI/SNF recruitment.The multifunctional Ccr4-Not complex directly promotes transcription elongationDisrupting vesicular trafficking at the endosome attenuates transcriptional activation by Gcn4.The yeast RNA polymerase II-associated factor Iwr1p is involved in the basal and regulated transcription of specific genes.The N-terminus and Tudor domains of Sgf29 are important for its heterochromatin boundary formation function.The TAF9 C-terminal conserved region domain is required for SAGA and TFIID promoter occupancy to promote transcriptional activation.Simultaneous recruitment of coactivators by Gcn4p stimulates multiple steps of transcription in vivo.The Saccharomyces cerevisiae Srb8-Srb11 complex functions with the SAGA complex during Gal4-activated transcription.The Spt4p subunit of yeast DSIF stimulates association of the Paf1 complex with elongating RNA polymerase II.A triad of subunits from the Gal11/tail domain of Srb mediator is an in vivo target of transcriptional activator Gcn4p.Interdependent recruitment of SAGA and Srb mediator by transcriptional activator Gcn4p.Nucleosome distortion as a possible mechanism of transcription activation domain functionMulti-tasking on chromatin with the SAGA coactivator complexes.Activator Gcn4p and Cyc8p/Tup1p are interdependent for promoter occupancy at ARG1 in vivoThe CCR4-NOT complex physically and functionally interacts with TRAMP and the nuclear exosome.Snf1p regulates Gcn5p transcriptional activity by antagonizing Spt3p.Mediator, TATA-binding protein, and RNA polymerase II contribute to low histone occupancy at active gene promoters in yeast.Integration of general amino acid control and target of rapamycin (TOR) regulatory pathways in nitrogen assimilation in yeast.SUMO functions in constitutive transcription and during activation of inducible genes in yeast.Accumulation of a threonine biosynthetic intermediate attenuates general amino acid control by accelerating degradation of Gcn4 via Pho85 and Cdk8.Nucleosome surface containing nucleosomal DNA entry/exit site regulates H3-K36me3 via association with RNA polymerase II and Set2.Distinct regulatory mechanisms of eukaryotic transcriptional activation by SAGA and TFIID.ATX1-generated H3K4me3 is required for efficient elongation of transcription, not initiation, at ATX1-regulated genesSWI/SNF binding to the HO promoter requires histone acetylation and stimulates TATA-binding protein recruitmentRsc4 connects the chromatin remodeler RSC to RNA polymerasesTranscriptional regulation in Saccharomyces cerevisiae: transcription factor regulation and function, mechanisms of initiation, and roles of activators and coactivators.Sumoylation of transcription factor Gcn4 facilitates its Srb10-mediated clearance from promoters in yeastYeast cap binding complex impedes recruitment of cleavage factor IA to weak termination sites.The Swi/Snf complex is important for histone eviction during transcriptional activation and RNA polymerase II elongation in vivoGenome-wide cooperation by HAT Gcn5, remodeler SWI/SNF, and chaperone Ydj1 in promoter nucleosome eviction and transcriptional activationHistone acetylation: truth of consequences?The cellular roles of Ccr4-NOT in model and pathogenic fungi-implications for fungal virulenceRecruitment of the ArgR/Mcm1p repressor is stimulated by the activator Gcn4p: a self-checking activation mechanism.
P2860
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P2860
An array of coactivators is required for optimal recruitment of TATA binding protein and RNA polymerase II by promoter-bound Gcn4p.
description
2004 nî lūn-bûn
@nan
2004 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
An array of coactivators is re ...... se II by promoter-bound Gcn4p.
@ast
An array of coactivators is re ...... se II by promoter-bound Gcn4p.
@en
An array of coactivators is re ...... se II by promoter-bound Gcn4p.
@nl
type
label
An array of coactivators is re ...... se II by promoter-bound Gcn4p.
@ast
An array of coactivators is re ...... se II by promoter-bound Gcn4p.
@en
An array of coactivators is re ...... se II by promoter-bound Gcn4p.
@nl
prefLabel
An array of coactivators is re ...... se II by promoter-bound Gcn4p.
@ast
An array of coactivators is re ...... se II by promoter-bound Gcn4p.
@en
An array of coactivators is re ...... se II by promoter-bound Gcn4p.
@nl
P2093
P2860
P3181
P1476
An array of coactivators is re ...... se II by promoter-bound Gcn4p.
@en
P2093
Alan G Hinnebusch
Hongfang Qiu
Krishnamurthy Natarajan
Mark J Swanson
Sungpil Yoon
P2860
P304
P3181
P356
10.1128/MCB.24.10.4104-4117.2004
P407
P577
2004-05-01T00:00:00Z