Molecular genetics of the RNA polymerase II general transcriptional machinery
about
Why do hubs in the yeast protein interaction network tend to be essential: reexamining the connection between the network topology and essentialityIsolation and characterization of human orthologs of yeast CCR4-NOT complex subunits.The TFIID components human TAF(II)140 and Drosophila BIP2 (TAF(II)155) are novel metazoan homologues of yeast TAF(II)47 containing a histone fold and a PHD fingerSystematic analysis of the protein interaction network for the human transcription machinery reveals the identity of the 7SK capping enzymeA human RNA polymerase II complex containing factors that modify chromatin structureAssociation of herpes simplex virus type 1 ICP8 and ICP27 proteins with cellular RNA polymerase II holoenzymeThe transcription elongation factor CA150 interacts with RNA polymerase II and the pre-mRNA splicing factor SF1Acetylation of histones and transcription-related factorsp53 Stimulates TFIID-TFIIA-promoter complex assembly, and p53-T antigen complex inhibits TATA binding protein-TATA interactionMCM proteins are associated with RNA polymerase II holoenzymeTranscriptional cofactor CA150 regulates RNA polymerase II elongation in a TATA-box-dependent mannerCell-specific nucleolar localization of TBP-related factor 2A protein phosphatase functions to recycle RNA polymerase IIp53 and TFIIEalpha share a common binding site on the Tfb1/p62 subunit of TFIIHPrevalence of the initiator over the TATA box in human and yeast genes and identification of DNA motifs enriched in human TATA-less core promotersA code for transcription initiation in mammalian genomesThe C-terminal domain-phosphorylated IIO form of RNA polymerase II is associated with the transcription repressor NC2 (Dr1/DRAP1) and is required for transcription activation in human nuclear extractsThe carboxy terminus of the small subunit of TFIIE regulates the transition from transcription initiation to elongation by RNA polymerase IIStimulation of the XPB ATP-dependent helicase by the beta subunit of TFIIEMapping of transcription start sites in Saccharomyces cerevisiae using 5' SAGEEvidence that the Tfg1/Tfg2 dimer interface of TFIIF lies near the active center of the RNA polymerase II initiation complexThe largest subunit of RNA polymerase II from the Glaucocystophyta: functional constraint and short-branch exclusion in deep eukaryotic phylogeny.Synthetic promoter design for new microbial chassisStructure of a (Cys3His) zinc ribbon, a ubiquitous motif in archaeal and eucaryal transcriptionInteraction of the Mediator Head Module with RNA Polymerase IISPN1, a conserved gene identified by suppression of a postrecruitment-defective yeast TATA-binding protein mutantBur1 kinase is required for efficient transcription elongation by RNA polymerase II.Mutations in the histone fold domain of the TAF12 gene show synthetic lethality with the TAF1 gene lacking the TAF N-terminal domain (TAND) by different mechanisms from those in the SPT15 gene encoding the TATA box-binding protein (TBP)TFIIS elongation factor and Mediator act in conjunction during transcription initiation in vivoAn array of coactivators is required for optimal recruitment of TATA binding protein and RNA polymerase II by promoter-bound Gcn4p.Set1/COMPASS and Mediator are repurposed to promote epigenetic transcriptional memory.Activation of a poised RNAPII-dependent promoter requires both SAGA and mediator.Positive and negative functions of the SAGA complex mediated through interaction of Spt8 with TBP and the N-terminal domain of TFIIA.RPAP1, a novel human RNA polymerase II-associated protein affinity purified with recombinant wild-type and mutated polymerase subunitsRoles of transcription factor Mot3 and chromatin in repression of the hypoxic gene ANB1 in yeastSAGA binds TBP via its Spt8 subunit in competition with DNA: implications for TBP recruitment.The yeast RNA polymerase II-associated factor Iwr1p is involved in the basal and regulated transcription of specific genes.Functions of Saccharomyces cerevisiae TFIIF during transcription start site utilization.SALSA, a variant of yeast SAGA, contains truncated Spt7, which correlates with activated transcriptionA high resolution protein interaction map of the yeast Mediator complex.
P2860
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P2860
Molecular genetics of the RNA polymerase II general transcriptional machinery
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Molecular genetics of the RNA polymerase II general transcriptional machinery
@ast
Molecular genetics of the RNA polymerase II general transcriptional machinery
@en
type
label
Molecular genetics of the RNA polymerase II general transcriptional machinery
@ast
Molecular genetics of the RNA polymerase II general transcriptional machinery
@en
prefLabel
Molecular genetics of the RNA polymerase II general transcriptional machinery
@ast
Molecular genetics of the RNA polymerase II general transcriptional machinery
@en
P2860
P3181
P1476
Molecular genetics of the RNA polymerase II general transcriptional machinery
@en
P2093
P2860
P304
P3181
P407
P577
1998-06-01T00:00:00Z