Artificially recruited TATA-binding protein fails to remodel chromatin and does not activate three promoters that require chromatin remodeling.
about
Cloning and characterization of hELD/OSA1, a novel BRG1 interacting proteinSpecific TATAA and bZIP requirements suggest that HTLV-I Tax has transcriptional activity subsequent to the assembly of an initiation complexArtificial recruitment of certain Mediator components affects requirement of basal transcription factor IIE.Protein-protein interaction map for yeast TFIID.Comparison of ABF1 and RAP1 in chromatin opening and transactivator potentiation in the budding yeast Saccharomyces cerevisiaeGlobal and specific transcriptional repression by the histone H3 amino terminus in yeastBayesPI - a new model to study protein-DNA interactions: a case study of condition-specific protein binding parameters for Yeast transcription factorsPromoter occupancy is a major determinant of chromatin remodeling enzyme requirements.GCN5 dependence of chromatin remodeling and transcriptional activation by the GAL4 and VP16 activation domains in budding yeast.Getting into chromatin: how do transcription factors get past the histones?Transcriptional regulation in Saccharomyces cerevisiae: transcription factor regulation and function, mechanisms of initiation, and roles of activators and coactivators.Artificial recruitment of mediator by the DNA-binding domain of Adr1 overcomes glucose repression of ADH2 expressionChromatin-dependent transcription factor accessibility rather than nucleosome remodeling predominates during global transcriptional restructuring in Saccharomyces cerevisiaeBinding of TATA binding protein to a naturally positioned nucleosome is facilitated by histone acetylation.The role of TFIIB-RNA polymerase II interaction in start site selection in yeast cellsGenome-wide analysis of the relationship between transcriptional regulation by Rpd3p and the histone H3 and H4 amino termini in budding yeast.Dispersed mutations in histone H3 that affect transcriptional repression and chromatin structure of the CHA1 promoter in Saccharomyces cerevisiae.The N-terminal and C-terminal domains of RAP1 are dispensable for chromatin opening and GCN4-mediated HIS4 activation in budding yeast.Specification of a DNA replication origin by a transcription complex.
P2860
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P2860
Artificially recruited TATA-binding protein fails to remodel chromatin and does not activate three promoters that require chromatin remodeling.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
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2000年學術文章
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name
Artificially recruited TATA-bi ...... require chromatin remodeling.
@en
Artificially recruited TATA-bi ...... require chromatin remodeling.
@nl
type
label
Artificially recruited TATA-bi ...... require chromatin remodeling.
@en
Artificially recruited TATA-bi ...... require chromatin remodeling.
@nl
prefLabel
Artificially recruited TATA-bi ...... require chromatin remodeling.
@en
Artificially recruited TATA-bi ...... require chromatin remodeling.
@nl
P2093
P2860
P1476
Artificially recruited TATA-bi ...... require chromatin remodeling.
@en
P2093
P2860
P304
P356
10.1128/MCB.20.16.5847-5857.2000
P407
P577
2000-08-01T00:00:00Z