Defects in the mRNA export factors Rat7p, Gle1p, Mex67p, and Rat8p cause hyperadenylation during 3'-end formation of nascent transcripts.
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A conserved CCCH-type zinc finger protein regulates mRNA nuclear adenylation and exportHuman immunodeficiency virus type 1 Tat increases the expression of cleavage and polyadenylation specificity factor 73-kilodalton subunit modulating cellular and viral expressionMolecular dissection of mRNA poly(A) tail length control in yeastDeterminants and implications of mRNA poly(A) tail size--does this protein make my tail look big?The nuclear exosome is active and important during budding yeast meiosis.Quality control of mRNA 3'-end processing is linked to the nuclear exosome.Tpa1p is part of an mRNP complex that influences translation termination, mRNA deadenylation, and mRNA turnover in Saccharomyces cerevisiae.Yeast poly(A)-binding protein, Pab1, and PAN, a poly(A) nuclease complex recruited by Pab1, connect mRNA biogenesis to exportDual requirement for yeast hnRNP Nab2p in mRNA poly(A) tail length control and nuclear exportEarly recruitment of AU-rich element-containing mRNAs determines their cytosolic fate during iron deficiency.Gle2p is essential to induce adaptation of the export of bulk poly(A)+ mRNA to heat shock in Saccharomyces cerevisiae.The yeast Apq12 protein affects nucleocytoplasmic mRNA transport.Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodiesA cis-acting element known to block 3' mRNA degradation enhances expression of polyA-minus mRNA in wild-type yeast cells and phenocopies a ski mutantProcessing bodies require RNA for assembly and contain nontranslating mRNAsAberrant herpesvirus-induced polyadenylation correlates with cellular messenger RNA destruction.Kaposi's sarcoma-associated herpesvirus ORF57 protein binds and protects a nuclear noncoding RNA from cellular RNA decay pathways.Loss of nuclear poly(A)-binding protein 1 causes defects in myogenesis and mRNA biogenesis.A viral nuclear noncoding RNA binds re-localized poly(A) binding protein and is required for late KSHV gene expression.Nuclear import of cytoplasmic poly(A) binding protein restricts gene expression via hyperadenylation and nuclear retention of mRNA.Coupling of termination, 3' processing, and mRNA exportComputational modeling of eukaryotic mRNA turnover.NXF1/p15 heterodimers are essential for mRNA nuclear export in DrosophilaA novel function for Sam68: enhancement of HIV-1 RNA 3' end processing.Red1 promotes the elimination of meiosis-specific mRNAs in vegetatively growing fission yeast.An early function during transcription for the yeast mRNA export factor Dbp5p/Rat8p suggested by its genetic and physical interactions with transcription factor IIH componentsThe human nuclear poly(a)-binding protein promotes RNA hyperadenylation and decayDegradation of normal mRNA in the nucleus of Saccharomyces cerevisiae.Synthetic genetic array analysis in Saccharomyces cerevisiae provides evidence for an interaction between RAT8/DBP5 and genes encoding P-body components.Cordycepin interferes with 3' end formation in yeast independently of its potential to terminate RNA chain elongation.Host shutoff is a conserved phenotype of gammaherpesvirus infection and is orchestrated exclusively from the cytoplasm.Assembly of an export-competent mRNP is needed for efficient release of the 3'-end processing complex after polyadenylationMessenger RNA export from the nucleus: a series of molecular wardrobe changes.RNA degradation in Saccharomyces cerevisaeNuclear imprisonment: viral strategies to arrest host mRNA nuclear export.Viral factors reveal a role for REF/Aly in nuclear RNA stability.New kid on the ID block: neural functions of the Nab2/ZC3H14 class of Cys₃His tandem zinc-finger polyadenosine RNA binding proteins.Nuclear pre-mRNA decapping and 5' degradation in yeast require the Lsm2-8p complex.The decapping activator Edc3 and the Q/N-rich domain of Lsm4 function together to enhance mRNA stability and alter mRNA decay pathway dependence in Saccharomyces cerevisiae.Recognition of polyadenosine RNA by the zinc finger domain of nuclear poly(A) RNA-binding protein 2 (Nab2) is required for correct mRNA 3'-end formation.
P2860
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P2860
Defects in the mRNA export factors Rat7p, Gle1p, Mex67p, and Rat8p cause hyperadenylation during 3'-end formation of nascent transcripts.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
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2001年學術文章
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name
Defects in the mRNA export fac ...... mation of nascent transcripts.
@en
Defects in the mRNA export fac ...... mation of nascent transcripts.
@nl
type
label
Defects in the mRNA export fac ...... mation of nascent transcripts.
@en
Defects in the mRNA export fac ...... mation of nascent transcripts.
@nl
prefLabel
Defects in the mRNA export fac ...... mation of nascent transcripts.
@en
Defects in the mRNA export fac ...... mation of nascent transcripts.
@nl
P2860
P1433
P1476
Defects in the mRNA export fac ...... mation of nascent transcripts.
@en
P2093
P2860
P304
P356
10.1017/S1355838201010147
P407
P577
2001-05-01T00:00:00Z