Mutations that suppress the deletion of an upstream activating sequence in yeast: involvement of a protein kinase and histone H3 in repressing transcription in vivo
about
Dissection of Pol II trigger loop function and Pol II activity-dependent control of start site selection in vivoPurification and biochemical heterogeneity of the mammalian SWI-SNF complexCharacterization of mutations that suppress the temperature-sensitive growth of the hpr1 delta mutant of Saccharomyces cerevisiae.Direct stimulation of transcription by negative cofactor 2 (NC2) through TATA-binding protein (TBP)Bur1 kinase is required for efficient transcription elongation by RNA polymerase II.SPT10 and SPT21 are required for transcription of particular histone genes in Saccharomyces cerevisiae.Phosphorylation of the RNA polymerase II carboxy-terminal domain by the Bur1 cyclin-dependent kinaseCooperative action of NC2 and Mot1p to regulate TATA-binding protein function across the genomeThe Dr1/DRAP1 heterodimer is a global repressor of transcription in vivo.Kin28 is found within TFIIH and a Kin28-Ccl1-Tfb3 trimer complex with differential sensitivities to T-loop phosphorylation.BUR1 and BUR2 encode a divergent cyclin-dependent kinase-cyclin complex important for transcription in vivo.Global regulation by the yeast Spt10 protein is mediated through chromatin structure and the histone upstream activating sequence elements.Sth1p, a Saccharomyces cerevisiae Snf2p/Swi2p homolog, is an essential ATPase in RSC and differs from Snf/Swi in its interactions with histones and chromatin-associated proteins.A functional module of yeast mediator that governs the dynamic range of heat-shock gene expressionHigh-affinity DNA binding by a Mot1p-TBP complex: implications for TAF-independent transcription.Genetic analysis connects SLX5 and SLX8 to the SUMO pathway in Saccharomyces cerevisiae.SNF11, a new component of the yeast SNF-SWI complex that interacts with a conserved region of SNF2.The Spt4p subunit of yeast DSIF stimulates association of the Paf1 complex with elongating RNA polymerase II.Evidence that Spt4, Spt5, and Spt6 control transcription elongation by RNA polymerase II in Saccharomyces cerevisiaeRegulation of histone modification and cryptic transcription by the Bur1 and Paf1 complexes.Analysis of transcriptional activation at a distance in Saccharomyces cerevisiae.Targeted histone acetylation at the yeast CUP1 promoter requires the transcriptional activator, the TATA boxes, and the putative histone acetylase encoded by SPT10.Sfh1p, a component of a novel chromatin-remodeling complex, is required for cell cycle progression.Spt16-Pob3 and the HMG protein Nhp6 combine to form the nucleosome-binding factor SPN.Functional antagonism between RNA polymerase II holoenzyme and global negative regulator NC2 in vivo.Physical and genetic associations of the Irc20 ubiquitin ligase with Cdc48 and SUMO.Genetic interactions of Spt4-Spt5 and TFIIS with the RNA polymerase II CTD and CTD modifying enzymes in Saccharomyces cerevisiaePhosphorylation of Not4p functions parallel to BUR2 to regulate resistance to cellular stresses in Saccharomyces cerevisiaeRNA Polymerase II C-Terminal Domain: Tethering Transcription to Transcript and TemplateMolecular genetics of the RNA polymerase II general transcriptional machineryA novel histone H4 mutant defective in nuclear division and mitotic chromosome transmission.Insights into the role of histone H3 and histone H4 core modifiable residues in Saccharomyces cerevisiae.Interplay of positive and negative regulators in transcription initiation by RNA polymerase II holoenzyme.An investigation of a role for U2 snRNP spliceosomal components in regulating transcriptionRNA polymerase II carboxy-terminal domain kinases: emerging clues to their function.Genetic and physical interactions between yeast RGR1 and SIN4 in chromatin organization and transcriptional regulation.RNA polymerase II transcription elongation and Pol II CTD Ser2 phosphorylation: A tail of two kinases.Activation of the Bur1-Bur2 cyclin-dependent kinase complex by Cak1.Cyclin-dependent kinase 9 (Cdk9) of fission yeast is activated by the CDK-activating kinase Csk1, overlaps functionally with the TFIIH-associated kinase Mcs6, and associates with the mRNA cap methyltransferase Pcm1 in vivoA TATA binding protein mutant with increased affinity for DNA directs transcription from a reversed TATA sequence in vivo.
P2860
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P2860
Mutations that suppress the deletion of an upstream activating sequence in yeast: involvement of a protein kinase and histone H3 in repressing transcription in vivo
description
1993 nî lūn-bûn
@nan
1993 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Mutations that suppress the de ...... pressing transcription in vivo
@ast
Mutations that suppress the de ...... pressing transcription in vivo
@en
type
label
Mutations that suppress the de ...... pressing transcription in vivo
@ast
Mutations that suppress the de ...... pressing transcription in vivo
@en
prefLabel
Mutations that suppress the de ...... pressing transcription in vivo
@ast
Mutations that suppress the de ...... pressing transcription in vivo
@en
P2860
P1433
P1476
Mutations that suppress the de ...... pressing transcription in vivo
@en
P2093
P2860
P304
P407
P577
1993-11-01T00:00:00Z