Saccharomyces cerevisiae transcription elongation mutants are defective in PUR5 induction in response to nucleotide depletion.
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Dissection of Pol II trigger loop function and Pol II activity-dependent control of start site selection in vivoRegulon-specific control of transcription elongation across the yeast genomeFunctional distinctions between IMP dehydrogenase genes in providing mycophenolate resistance and guanine prototrophy to yeastOpposing roles for Set2 and yFACT in regulating TBP binding at promotersMolecular evidence for a positive role of Spt4 in transcription elongation.SDT1/SSM1, a multicopy suppressor of S-II null mutant, encodes a novel pyrimidine 5'-nucleotidase.Genetic evidence supports a role for the yeast CCR4-NOT complex in transcriptional elongation.RNA polymerase II elongation factors of Saccharomyces cerevisiae: a targeted proteomics approachInteraction between transcription elongation factors and mRNA 3'-end formation at the Saccharomyces cerevisiae GAL10-GAL7 locus.Stimulation of RNA polymerase II transcript cleavage activity contributes to maintain transcriptional fidelity in yeast.mRNA capping enzyme activity is coupled to an early transcription elongationRole for the Ssu72 C-terminal domain phosphatase in RNA polymerase II transcription elongation.Ctr9, Rtf1, and Leo1 are components of the Paf1/RNA polymerase II complex.The Paf1 complex physically and functionally associates with transcription elongation factors in vivo.The prefoldin complex regulates chromatin dynamics during transcription elongationNpl3 is an antagonist of mRNA 3' end formation by RNA polymerase II.Transcription elongation factor S-II maintains transcriptional fidelity and confers oxidative stress resistance.Evidence that the elongation factor TFIIS plays a role in transcription initiation at GAL1 in Saccharomyces cerevisiae.Characterization of a six-subunit holo-elongator complex required for the regulated expression of a group of genes in Saccharomyces cerevisiae.Phenotypic consequences of purine nucleotide imbalance in Saccharomyces cerevisiaeHistone variant H2A.Z and RNA polymerase II transcription elongation.Regulation of an IMP dehydrogenase gene and its overexpression in drug-sensitive transcription elongation mutants of yeast.Analysis of gene induction and arrest site transcription in yeast with mutations in the transcription elongation machineryTranscription elongation factor S-II is required for definitive hematopoiesis.Sub1 associates with Spt5 and influences RNA polymerase II transcription elongation rateDistinguishing the roles of Topoisomerases I and II in relief of transcription-induced torsional stress in yeast rRNA genes.DRL1, a homolog of the yeast TOT4/KTI12 protein, has a function in meristem activity and organ growth in plants.Requirement for yeast RAD26, a homolog of the human CSB gene, in elongation by RNA polymerase IIWide-ranging and unexpected consequences of altered Pol II catalytic activity in vivo.Mutations in the RNA polymerase III subunit Rpc11p that decrease RNA 3' cleavage activity increase 3'-terminal oligo(U) length and La-dependent tRNA processingSeparable functions of the fission yeast Spt5 carboxyl-terminal domain (CTD) in capping enzyme binding and transcription elongation overlap with those of the RNA polymerase II CTDTFIIS enhances transcriptional elongation through an artificial arrest site in vivo.The peptidyl prolyl isomerase Rrd1 regulates the elongation of RNA polymerase II during transcriptional stresses.The yeast pafl-rNA polymerase II complex is required for full expression of a subset of cell cycle-regulated genes.Nucleolar stress with and without p53.Genome-wide analysis of mRNA stability using transcription inhibitors and microarrays reveals posttranscriptional control of ribosome biogenesis factors.Accumulation of unstable promoter-associated transcripts upon loss of the nuclear exosome subunit Rrp6p in Saccharomyces cerevisiae.Deconvolution of chromatin immunoprecipitation-microarray (ChIP-chip) analysis of MBF occupancies reveals the temporal recruitment of Rep2 at the MBF target genesMutations in the Saccharomyces cerevisiae RPB1 gene conferring hypersensitivity to 6-azauracil.Defects in SPT16 or POB3 (yFACT) in Saccharomyces cerevisiae cause dependence on the Hir/Hpc pathway: polymerase passage may degrade chromatin structure.
P2860
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P2860
Saccharomyces cerevisiae transcription elongation mutants are defective in PUR5 induction in response to nucleotide depletion.
description
2000 nî lūn-bûn
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2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Saccharomyces cerevisiae trans ...... ponse to nucleotide depletion.
@ast
Saccharomyces cerevisiae trans ...... ponse to nucleotide depletion.
@en
Saccharomyces cerevisiae trans ...... ponse to nucleotide depletion.
@nl
type
label
Saccharomyces cerevisiae trans ...... ponse to nucleotide depletion.
@ast
Saccharomyces cerevisiae trans ...... ponse to nucleotide depletion.
@en
Saccharomyces cerevisiae trans ...... ponse to nucleotide depletion.
@nl
prefLabel
Saccharomyces cerevisiae trans ...... ponse to nucleotide depletion.
@ast
Saccharomyces cerevisiae trans ...... ponse to nucleotide depletion.
@en
Saccharomyces cerevisiae trans ...... ponse to nucleotide depletion.
@nl
P2860
P3181
P1476
Saccharomyces cerevisiae trans ...... ponse to nucleotide depletion.
@en
P2093
P2860
P304
P3181
P356
10.1128/MCB.20.20.7427-7437.2000
P407
P577
2000-10-01T00:00:00Z