In vitro analysis of a transcription termination site for RNA polymerase II.
about
The RNA cleavage activity of RNA polymerase III is mediated by an essential TFIIS-like subunit and is important for transcription terminationDown-regulation of Rous sarcoma virus long terminal repeat promoter activity by a HeLa cell basic proteinMutations in the second largest subunit of RNA polymerase II cause 6-azauracil sensitivity in yeast and increased transcriptional arrest in vitroAmanitin greatly reduces the rate of transcription by RNA polymerase II ternary complexes but fails to inhibit some transcript cleavage modesNon-templated addition of nucleotides to the 3' end of nascent RNA during RNA editing in PhysarumAnalysis of gene induction and arrest site transcription in yeast with mutations in the transcription elongation machineryInappropriate transcription from the 5' end of the murine dihydrofolate reductase gene masks transcriptional regulationSarkosyl block of transcription reinitiation by RNA polymerase II as visualized by the colliding polymerases reinitiation assay.Identification of a decay in transcription potential that results in elongation factor dependence of RNA polymerase II.Identification of a 3'-->5' exonuclease activity associated with human RNA polymerase II.Transcriptional arrest of yeast RNA polymerase II by Escherichia coli rho protein in vitroTranscription elongation in the human c-myc gene is governed by overall transcription initiation levels in Xenopus oocytes.Functional analysis of a stable transcription arrest site in the first intron of the murine adenosine deaminase gene.Analysis of premature termination in c-myc during transcription by RNA polymerase II in a HeLa nuclear extract.A heat-labile factor promotes premature 3' end formation in exon 1 of the murine adenosine deaminase gene in a cell-free transcription system.Stability of Drosophila RNA polymerase II elongation complexes in vitro.In vitro transcription of baculovirus immediate early genes: accurate mRNA initiation by nuclear extracts from both insect and human cells.Characterization of a novel RNA polymerase II arrest site which lacks a weak 3' RNA-DNA hybrid.The downstream regulatory sequence of the adenovirus type 2 major late promoter is functionally redundant.Control of formation of two distinct classes of RNA polymerase II elongation complexes.Hpr1 is preferentially required for transcription of either long or G+C-rich DNA sequences in Saccharomyces cerevisiae.3' Processing and termination of mouse histone transcripts synthesized in vitro by RNA polymerase II.Regulation of eukaryotic gene expression by transcriptional attenuation.Cooperation between upstream and downstream elements of the adenovirus major late promoter for maximal late phase-specific transcription.Sequence-Modified Antibiotic Resistance Genes Provide Sustained Plasmid-Mediated Transgene Expression in Mammals.
P2860
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P2860
In vitro analysis of a transcription termination site for RNA polymerase II.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
1990年论文
@zh
1990年论文
@zh-cn
name
In vitro analysis of a transcription termination site for RNA polymerase II.
@ast
In vitro analysis of a transcription termination site for RNA polymerase II.
@en
type
label
In vitro analysis of a transcription termination site for RNA polymerase II.
@ast
In vitro analysis of a transcription termination site for RNA polymerase II.
@en
prefLabel
In vitro analysis of a transcription termination site for RNA polymerase II.
@ast
In vitro analysis of a transcription termination site for RNA polymerase II.
@en
P2860
P356
P1476
In vitro analysis of a transcription termination site for RNA polymerase II.
@en
P2093
P2860
P304
P356
10.1128/MCB.10.11.5782
P407
P577
1990-11-01T00:00:00Z