Point mutations upstream of the yeast ADH2 poly(A) site significantly reduce the efficiency of 3'-end formation.
about
The ESS1 prolyl isomerase and its suppressor BYE1 interact with RNA pol II to inhibit transcription elongation in Saccharomyces cerevisiae.Organization and function of APT, a subcomplex of the yeast cleavage and polyadenylation factor involved in the formation of mRNA and small nucleolar RNA 3'-ends.A mutation in GRS1, a glycyl-tRNA synthetase, affects 3'-end formation in Saccharomyces cerevisiaeNpl3 is an antagonist of mRNA 3' end formation by RNA polymerase II.Formation of mRNA 3' ends in eukaryotes: mechanism, regulation, and interrelationships with other steps in mRNA synthesisFlexibility and interchangeability of polyadenylation signals in Saccharomyces cerevisiaeTranscription termination downstream of the Saccharomyces cerevisiae FBP1 [changed from FPB1] poly(A) site does not depend on efficient 3'end processing.Different modes of regulation of transcription and pre-mRNA processing of the structurally juxtaposed homologs, Rnf33 and Rnf35, in eggs and in pre-implantation embryos.Recognition of polyadenylation sites in yeast pre-mRNAs by cleavage and polyadenylation factorSaturation mutagenesis of a polyadenylation signal reveals a hexanucleotide element essential for mRNA 3' end formation in Saccharomyces cerevisiae.Functional analysis of mRNA 3' end formation signals in the convergent and overlapping transcription units of the S. cerevisiae genes RHO1 and MRP2A genome-wide analysis indicates that yeast pre-mRNA splicing is predominantly posttranscriptional.The end of the message: 3'-end processing leading to polyadenylated messenger RNA.3'-end-forming signals of yeast mRNA.RNA polymerase II mutations conferring defects in poly(A) site cleavage and termination in Saccharomyces cerevisiaeTSF3, a global regulatory protein that silences transcription of yeast GAL genes, also mediates repression by alpha 2 repressor and is identical to SIN4.Identification of pre-mRNA polyadenylation sites in Saccharomyces cerevisiaeDifferent sequence elements are required for function of the cauliflower mosaic virus polyadenylation site in Saccharomyces cerevisiae compared with in plants.Conditional defect in mRNA 3' end processing caused by a mutation in the gene for poly(A) polymeraseSignals that produce 3' termini in CYC1 mRNA of the yeast Saccharomyces cerevisiae.Poly(A) site selection in the yeast Ty retroelement requires an upstream region and sequence-specific titratable factor(s) in vitro.The Drosophila melanogaster suppressor of Hairy-wing zinc finger protein has minimal effects on gene expression in Saccharomyces cerevisiae.Saccharomyces cerevisiae gene expression changes during rotating wall vessel suspension culture.Molecular analysis of the malic enzyme gene (mae2) of Schizosaccharomyces pombe.Transcriptional terminators of RNA polymerase II are associated with yeast replication origins.Sequence requirements of the bidirectional yeast TRP4 mRNA 3'-end formation signal.In vivo evidence that defects in the transcriptional elongation factors RPB2, TFIIS, and SPT5 enhance upstream poly(A) site utilization.A complex unidirectional signal element mediates GCN4 mRNA 3' end formation in Saccharomyces cerevisiae.Pre-mRNA topology is important for 3'-end formation in Saccharomyces cerevisiae and mammals.Sequences regulating temporal poly(A) site switching in the adenovirus major late transcription unit.Separation of factors required for cleavage and polyadenylation of yeast pre-mRNA.The contribution of AAUAAA and the upstream element UUUGUA to the efficiency of mRNA 3'-end formation in plants.RNA 3' end signals of the S.pombe ura4 gene comprise a site determining and efficiency elementHomologous mRNA 3' end formation in fission and budding yeast.Functional interaction of the Ess1 prolyl isomerase with components of the RNA polymerase II initiation and termination machineriesTermination and pausing of RNA polymerase II downstream of yeast polyadenylation sitesTranscriptional termination signals for RNA polymerase II in fission yeast.Unusual aspects of in vitro RNA processing in the 3' regions of the GAL1, GAL7, and GAL10 genes in Saccharomyces cerevisiae.Several distinct types of sequence elements are required for efficient mRNA 3' end formation in a pea rbcS gene.Binding to Elongin C inhibits degradation of interacting proteins in yeast.
P2860
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P2860
Point mutations upstream of the yeast ADH2 poly(A) site significantly reduce the efficiency of 3'-end formation.
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
1991年论文
@zh
1991年论文
@zh-cn
name
Point mutations upstream of th ...... fficiency of 3'-end formation.
@ast
Point mutations upstream of th ...... fficiency of 3'-end formation.
@en
type
label
Point mutations upstream of th ...... fficiency of 3'-end formation.
@ast
Point mutations upstream of th ...... fficiency of 3'-end formation.
@en
prefLabel
Point mutations upstream of th ...... fficiency of 3'-end formation.
@ast
Point mutations upstream of th ...... fficiency of 3'-end formation.
@en
P2093
P2860
P356
P1476
Point mutations upstream of th ...... fficiency of 3'-end formation.
@en
P2093
J Whoriskey
S H Seiler
P2860
P304
P356
10.1128/MCB.11.4.2004
P407
P577
1991-04-01T00:00:00Z