The constitutive transport element (CTE) of Mason-Pfizer monkey virus (MPMV) accesses a cellular mRNA export pathway.
about
Specific interaction between RNA helicase A and Tap, two cellular proteins that bind to the constitutive transport element of type D retrovirusTAP (NXF1) belongs to a multigene family of putative RNA export factors with a conserved modular architectureLocalization of nucleoporin Tpr to the nuclear pore complex is essential for Tpr mediated regulation of the export of unspliced RNA.Herpes simplex virus ICP27 protein directly interacts with the nuclear pore complex through Nup62, inhibiting host nucleocytoplasmic transport pathwaysMatrin 3 is a co-factor for HIV-1 Rev in regulating post-transcriptional viral gene expressionNucleoporins nup98 and nup214 participate in nuclear export of human immunodeficiency virus type 1 RevInhibition of human immunodeficiency virus Rev and human T-cell leukemia virus Rex function, but not Mason-Pfizer monkey virus constitutive transport element activity, by a mutant human nucleoporin targeted to Crm1TAP binds to the constitutive transport element (CTE) through a novel RNA-binding motif that is sufficient to promote CTE-dependent RNA export from the nucleusFormation of Tap/NXT1 heterodimers activates Tap-dependent nuclear mRNA export by enhancing recruitment to nuclear pore complexesThe C-terminal domain of TAP interacts with the nuclear pore complex and promotes export of specific CTE-bearing RNA substratesNXT1 (p15) is a crucial cellular cofactor in TAP-dependent export of intron-containing RNA in mammalian cells.Mex67p of Schizosaccharomyces pombe interacts with Rae1p in mediating mRNA exportRanGTP-binding protein NXT1 facilitates nuclear export of different classes of RNA in vitro.A role for RNA helicase A in post-transcriptional regulation of HIV type 1The carboxyl terminus of RNA helicase A contains a bidirectional nuclear transport domainPre-mRNA splicing alters mRNP composition: evidence for stable association of proteins at exon-exon junctionsThe nucleoporin nup153 plays a critical role in multiple types of nuclear exportCofactor requirements for nuclear export of Rev response element (RRE)- and constitutive transport element (CTE)-containing retroviral RNAs. An unexpected role for actin.SMN, the spinal muscular atrophy protein, forms a pre-import snRNP complex with snurportin1 and importin betatRNA-linked molecular beacons for imaging mRNAs in the cytoplasm of living cellsPre-mRNA processing enhancer (PPE) elements from intronless genes play additional roles in mRNA biogenesis than do ones from intron-containing genesRNA Export through the NPC in EukaryotesNuclear trafficking of retroviral RNAs and Gag proteins during late steps of replicationThe structure of the mRNA export factor TAP reveals a cis arrangement of a non-canonical RNP domain and an LRR domainThe crystal structure and mutational analysis of a novel RNA-binding domain found in the human Tap nuclear mRNA export factor.Binding of the Mex67p/Mtr2p heterodimer to FXFG, GLFG, and FG repeat nucleoporins is essential for nuclear mRNA export.The yeast hnRNP-Like proteins Yra1p and Yra2p participate in mRNA export through interaction with Mex67p.Nuclear export of messenger RNASam68, RNA helicase A and Tap cooperate in the post-transcriptional regulation of human immunodeficiency virus and type D retroviral mRNAU2AF participates in the binding of TAP (NXF1) to mRNAUsing viral species specificity to define a critical protein/RNA interaction surfaceREF, an evolutionary conserved family of hnRNP-like proteins, interacts with TAP/Mex67p and participates in mRNA nuclear export.RNA export mediated by tap involves NXT1-dependent interactions with the nuclear pore complexThe human Tap protein is a nuclear mRNA export factor that contains novel RNA-binding and nucleocytoplasmic transport sequencesEvolutionary conservation of a molecular machinery for export and expression of mRNAs with retained intronsTransport into and out of the nucleus.The exon-exon junction complex provides a binding platform for factors involved in mRNA export and nonsense-mediated mRNA decayTap and NXT promote translation of unspliced mRNA.Interferon-induced HERC5 is evolving under positive selection and inhibits HIV-1 particle production by a novel mechanism targeting Rev/RRE-dependent RNA nuclear export.An intron with a constitutive transport element is retained in a Tap messenger RNA.
P2860
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P2860
The constitutive transport element (CTE) of Mason-Pfizer monkey virus (MPMV) accesses a cellular mRNA export pathway.
description
1997 nî lūn-bûn
@nan
1997 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
The constitutive transport ele ...... cellular mRNA export pathway.
@ast
The constitutive transport ele ...... cellular mRNA export pathway.
@en
type
label
The constitutive transport ele ...... cellular mRNA export pathway.
@ast
The constitutive transport ele ...... cellular mRNA export pathway.
@en
prefLabel
The constitutive transport ele ...... cellular mRNA export pathway.
@ast
The constitutive transport ele ...... cellular mRNA export pathway.
@en
P2093
P2860
P356
P1433
P1476
The constitutive transport ele ...... cellular mRNA export pathway.
@en
P2093
A E Pasquinelli
J E Dahlberg
M L Hammarskjöld
P2860
P304
P356
10.1093/EMBOJ/16.24.7500
P407
P577
1997-12-01T00:00:00Z