The RNA polymerase II general transcription factors: past, present, and future.
about
Architecture of the RNA polymerase II-TFIIF complex revealed by cross-linking and mass spectrometry.Protein-protein interaction map for yeast TFIID.Separation of the Saccharomyces cerevisiae Paf1 complex from RNA polymerase II results in changes in its subnuclear localization.Dissociable Rpb4-Rpb7 subassembly of rna polymerase II binds to single-strand nucleic acid and mediates a post-recruitment step in transcription initiation.BRFU, a TFIIB-like factor, is directly recruited to the TATA-box of polymerase III small nuclear RNA gene promoters through its interaction with TATA-binding proteinA high-resolution map of active promoters in the human genomePurification and identification of proteins that bind to the hereditary persistence of fetal hemoglobin -198 mutation in the gamma-globin gene promoterATG deserts define a novel core promoter subclass.Widespread use of TATA elements in the core promoters for RNA polymerases III, II, and I in fission yeastThree novel downstream promoter elements regulate MHC class I promoter activity in mammalian cellsThe fission yeast TFIIB-related factor limits RNA polymerase III to a TATA-dependent pathway of TBP recruitment.Distinct transcriptional pathways regulate basal and activated major histocompatibility complex class I expression.Full and partial genome-wide assembly and disassembly of the yeast transcription machinery in response to heat shockTwo type III effector genes of Xanthomonas oryzae pv. oryzae control the induction of the host genes OsTFIIAgamma1 and OsTFX1 during bacterial blight of riceSIRT1-dependent regulation of chromatin and transcription: linking NAD(+) metabolism and signaling to the control of cellular functionsStructural basis of transcription initiation by RNA polymerase II.The RPB2 flap loop of human RNA polymerase II is dispensable for transcription initiation and elongation.In vitro transcription of a torsionally constrained template.Efficient reconstitution of transcription elongation complexes for single-molecule studies of eukaryotic RNA polymerase II.Interaction between P-TEFb and the C-terminal domain of RNA polymerase II activates transcriptional elongation from sites upstream or downstream of target genes.Collaborative competition mechanism for gene activation in vivo.TFIIB-facilitated recruitment of preinitiation complexes by a TAF-independent mechanism.The sensitivity of RNA polymerase II in elongation complexes to C-terminal domain phosphatase.Purification and enzymic properties of Mot1 ATPase, a regulator of basal transcription in the yeast Saccharomyces cerevisiae.Mutations in the TATA-binding protein, affecting transcriptional activation, show synthetic lethality with the TAF145 gene lacking the TAF N-terminal domain in Saccharomyces cerevisiae.Genomics basics: DNA structure, gene expression, cloning, genetic mapping, and molecular tests.
P2860
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P2860
The RNA polymerase II general transcription factors: past, present, and future.
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
name
The RNA polymerase II general transcription factors: past, present, and future.
@ast
The RNA polymerase II general transcription factors: past, present, and future.
@en
type
label
The RNA polymerase II general transcription factors: past, present, and future.
@ast
The RNA polymerase II general transcription factors: past, present, and future.
@en
prefLabel
The RNA polymerase II general transcription factors: past, present, and future.
@ast
The RNA polymerase II general transcription factors: past, present, and future.
@en
P2093
P2860
P356
P1476
The RNA polymerase II general transcription factors: past, present, and future
@en
P2093
D Reinberg
E Maldonado
F Mermelstein
G Orphanides
P2860
P304
P356
10.1101/SQB.1998.63.83
P577
1998-01-01T00:00:00Z