A nuclear translation-like factor eIF4AIII is recruited to the mRNA during splicing and functions in nonsense-mediated decay
about
The signal sequence coding region promotes nuclear export of mRNATranslation repression in human cells by microRNA-induced gene silencing requires RCK/p54Biochemical analysis of the EJC reveals two new factors and a stable tetrameric protein coreThe proteins PDIP3 and ZC11A associate with the human TREX complex in an ATP-dependent manner and function in mRNA exportATP is required for interactions between UAP56 and two conserved mRNA export proteins, Aly and CIP29, to assemble the TREX complexBinding of a novel SMG-1-Upf1-eRF1-eRF3 complex (SURF) to the exon junction complex triggers Upf1 phosphorylation and nonsense-mediated mRNA decayeIF4G is required for the pioneer round of translation in mammalian cellsAly and THO are required for assembly of the human TREX complex and association of TREX components with the spliced mRNAHuman DDX3 functions in translation and interacts with the translation initiation factor eIF3Functions of hUpf3a and hUpf3b in nonsense-mediated mRNA decay and translationPoly(A) binding protein (PABP) homeostasis is mediated by the stability of its inhibitor, Paip2Stimulation of mammalian translation initiation factor eIF4A activity by a small molecule inhibitor of eukaryotic translation.mRNA decay during herpes simplex virus (HSV) infections: protein-protein interactions involving the HSV virion host shutoff protein and translation factors eIF4H and eIF4A.Mutational analysis of human eIF4AIII identifies regions necessary for exon junction complex formation and nonsense-mediated mRNA decay.Proteomic analysis of interchromatin granule clustersDead-box proteins: a family affair--active and passive players in RNP-remodelingInhibition of ribosome recruitment induces stress granule formation independently of eukaryotic initiation factor 2alpha phosphorylationSplicing remodels messenger ribonucleoprotein architecture via eIF4A3-dependent and -independent recruitment of exon junction complex componentsA role for the eIF4E-binding protein 4E-T in P-body formation and mRNA decayAn interaction between two RNA binding proteins, Nab2 and Pub1, links mRNA processing/export and mRNA stability.The exon junction core complex is locked onto RNA by inhibition of eIF4AIII ATPase activityExpression of the core exon-junction complex factor eukaryotic initiation factor 4A3 is increased during spatial exploration and striatally-mediated learningIdentification of a signature motif for the eIF4a3-SECIS interactionA proteomic comparison of immature and mature mouse gonadotrophs reveals novel differentially expressed nuclear proteins that regulate gonadotropin gene transcription and RNA splicingInhibition of Nonsense-mediated mRNA Decay by the Natural Product Pateamine A through Eukaryotic Initiation Factor 4AIIIRNA helicase A is necessary for translation of selected messenger RNAs.Epigenetic activation of a subset of mRNAs by eIF4E explains its effects on cell proliferationSelective pharmacological targeting of a DEAD box RNA helicase.Comparison of nonsense-mediated mRNA decay efficiency in various murine tissues.Splicing of U12-type introns deposits an exon junction complex competent to induce nonsense-mediated mRNA decay.Pea p68, a DEAD-box helicase, provides salinity stress tolerance in transgenic tobacco by reducing oxidative stress and improving photosynthesis machineryControl of VP16 translation by the herpes simplex virus type 1 immediate-early protein ICP27.Retention of spliceosomal components along ligated exons ensures efficient removal of multiple intronsNuclear translation visualized by ribosome-bound nascent chain puromycylation.Identification of a novel nucleocytoplasmic shuttling RNA helicase of trypanosomes.Transcriptome-wide characterization of the eIF4A signature highlights plasticity in translation regulation.eIF4AIII enhances translation of nuclear cap-binding complex-bound mRNAs by promoting disruption of secondary structures in 5'UTR.The two eIF4A helicases in Trypanosoma brucei are functionally distinct.RNA aptamers to mammalian initiation factor 4G inhibit cap-dependent translation by blocking the formation of initiation factor complexes.An alternative branch of the nonsense-mediated decay pathway
P2860
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P2860
A nuclear translation-like factor eIF4AIII is recruited to the mRNA during splicing and functions in nonsense-mediated decay
description
2004 nî lūn-bûn
@nan
2004 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մարտին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
A nuclear translation-like fac ...... ons in nonsense-mediated decay
@ast
A nuclear translation-like fac ...... ons in nonsense-mediated decay
@en
A nuclear translation-like fac ...... ons in nonsense-mediated decay
@nl
type
label
A nuclear translation-like fac ...... ons in nonsense-mediated decay
@ast
A nuclear translation-like fac ...... ons in nonsense-mediated decay
@en
A nuclear translation-like fac ...... ons in nonsense-mediated decay
@nl
prefLabel
A nuclear translation-like fac ...... ons in nonsense-mediated decay
@ast
A nuclear translation-like fac ...... ons in nonsense-mediated decay
@en
A nuclear translation-like fac ...... ons in nonsense-mediated decay
@nl
P2093
P2860
P3181
P356
P1476
A nuclear translation-like fac ...... ons in nonsense-mediated decay
@en
P2093
Chung-Sheng Lee
Jeanne L Hsu
Lian Wee Ler
Maria A Ferraiuolo
Mauro Costa-Mattioli
Ming-Juan Luo
Robin Reed
P2860
P304
P3181
P356
10.1073/PNAS.0400933101
P407
P577
2004-03-23T00:00:00Z