scholarly article | Q13442814 |
P50 | author | Søren Lykke-Andersen | Q55136794 |
Edouard Bertrand | Q57645202 | ||
Torben Heick Jensen | Q42334328 | ||
P2093 | author name string | Claire Moore | |
Xiangping Qu | |||
Cyril Saguez | |||
Tommy Nasser | |||
P2860 | cites work | TREX is a conserved complex coupling transcription with messenger RNA export | Q24295211 |
Proteomic analysis identifies a new complex required for nuclear pre-mRNA retention and splicing | Q24317157 | ||
The RNA export factor Gle1p is located on the cytoplasmic fibrils of the NPC and physically interacts with the FG-nucleoporin Rip1p, the DEAD-box protein Rat8p/Dbp5p and a new protein Ymr 255p | Q24529891 | ||
Molecular dissection of mRNA poly(A) tail length control in yeast | Q24646300 | ||
Role of polyadenylation in nucleocytoplasmic transport of mRNA | Q24650446 | ||
Structure of the N-Terminal Mlp1-Binding Domain of the Saccharomyces cerevisiae mRNA-Binding Protein, Nab2 | Q27649526 | ||
A protein complex containing Tho2, Hpr1, Mft1 and a novel protein, Thp2, connects transcription elongation with mitotic recombination in Saccharomyces cerevisiae | Q27929512 | ||
The yeast THO complex and mRNA export factors link RNA metabolism with transcription and genome instability | Q27929526 | ||
Stable mRNP formation and export require cotranscriptional recruitment of the mRNA export factors Yra1p and Sub2p by Hpr1p | Q27929754 | ||
Hrp1, a sequence-specific RNA-binding protein that shuttles between the nucleus and the cytoplasm, is required for mRNA 3'-end formation in yeast | Q27930053 | ||
Pta1, a component of yeast CF II, is required for both cleavage and poly(A) addition of mRNA precursor | Q27930178 | ||
A protein that shuttles between the nucleus and the cytoplasm is an important mediator of RNA export | Q27931607 | ||
The mRNA export machinery requires the novel Sac3p-Thp1p complex to dock at the nucleoplasmic entrance of the nuclear pores | Q27931766 | ||
Nuclear mRNA surveillance in THO/sub2 mutants is triggered by inefficient polyadenylation | Q27931769 | ||
The yeast Pan2 protein is required for poly(A)-binding protein-stimulated poly(A)-nuclease activity | Q27931926 | ||
General, rapid, and transcription-dependent fragmentation of nucleolar antigens in S. cerevisiae mRNA export mutants | Q27932821 | ||
Dissecting mechanisms of nuclear mRNA surveillance in THO/sub2 complex mutants | Q27932830 | ||
Five subunits are required for reconstitution of the cleavage and polyadenylation activities of Saccharomyces cerevisiae cleavage factor I. | Q27933038 | ||
A genetic screen in Saccharomyces cerevisiae identifies new genes that interact with mex67-5, a temperature-sensitive allele of the gene encoding the mRNA export receptor. | Q27933172 | ||
Inositol hexakisphosphate and Gle1 activate the DEAD-box protein Dbp5 for nuclear mRNA export | Q27933519 | ||
Perinuclear Mlp proteins downregulate gene expression in response to a defect in mRNA export | Q27933999 | ||
Sus1, Sac3, and Thp1 mediate post-transcriptional tethering of active genes to the nuclear rim as well as to non-nascent mRNP. | Q27934062 | ||
Comprehensive analysis of diverse ribonucleoprotein complexes. | Q27934310 | ||
Yeast poly(A)-binding protein Pab1 shuttles between the nucleus and the cytoplasm and functions in mRNA export | Q27934431 | ||
Yeast poly(A)-binding protein, Pab1, and PAN, a poly(A) nuclease complex recruited by Pab1, connect mRNA biogenesis to export | Q27934476 | ||
Nuclear mRNA export requires complex formation between Mex67p and Mtr2p at the nuclear pores. | Q27934517 | ||
Dual requirement for yeast hnRNP Nab2p in mRNA poly(A) tail length control and nuclear export | Q27934522 | ||
A conditional allele of the novel repeat-containing yeast nucleoporin RAT7/NUP159 causes both rapid cessation of mRNA export and reversible clustering of nuclear pore complexes | Q27934541 | ||
Npl3 is an antagonist of mRNA 3' end formation by RNA polymerase II. | Q27935622 | ||
Activation of the DExD/H-box protein Dbp5 by the nuclear-pore protein Gle1 and its coactivator InsP6 is required for mRNA export | Q27935795 | ||
A novel yeast gene, THO2, is involved in RNA pol II transcription and provides new evidence for transcriptional elongation-associated recombination. | Q27936954 | ||
A new hyperrecombination mutation identifies a novel yeast gene, THP1, connecting transcription elongation with mitotic recombination | Q27937094 | ||
Effects of mutations in the Saccharomyces cerevisiae RNA14, RNA15, and PAP1 genes on polyadenylation in vivo | Q27937493 | ||
Dbp5p/Rat8p is a yeast nuclear pore-associated DEAD-box protein essential for RNA export | Q27937989 | ||
Functional specificity of shuttling hnRNPs revealed by genome-wide analysis of their RNA binding profiles | Q27938114 | ||
Messenger RNAs are recruited for nuclear export during transcription | Q27938581 | ||
Interactions between mRNA export commitment, 3'-end quality control, and nuclear degradation | Q27938985 | ||
Splicing factor Sub2p is required for nuclear mRNA export through its interaction with Yra1p | Q27939091 | ||
The DECD box putative ATPase Sub2p is an early mRNA export factor | Q27939448 | ||
Polyadenylation site choice in yeast is affected by competition between Npl3 and polyadenylation factor CFI. | Q27939878 | ||
Nuclear retention of unspliced mRNAs in yeast is mediated by perinuclear Mlp1. | Q27939910 | ||
Mex67p, a novel factor for nuclear mRNA export, binds to both poly(A)+ RNA and nuclear pores | Q27940054 | ||
The tandem affinity purification (TAP) method: a general procedure of protein complex purification | Q28131621 | ||
Construction of a set of convenient Saccharomyces cerevisiae strains that are isogenic to S288C | Q28131625 | ||
The Glc7p nuclear phosphatase promotes mRNA export by facilitating association of Mex67p with mRNA | Q75399914 | ||
Assembly of export-competent mRNP: it's all about being connected | Q83283711 | ||
Exporting RNA from the nucleus to the cytoplasm | Q28245155 | ||
Transitions in RNA polymerase II elongation complexes at the 3' ends of genes | Q29614767 | ||
The essential N terminus of the Pta1 scaffold protein is required for snoRNA transcription termination and Ssu72 function but is dispensable for pre-mRNA 3'-end processing. | Q30663144 | ||
Mutations in the yeast RNA14 and RNA15 genes result in an abnormal mRNA decay rate; sequence analysis reveals an RNA-binding domain in the RNA15 protein | Q33245533 | ||
A block to mRNA nuclear export in S. cerevisiae leads to hyperadenylation of transcripts that accumulate at the site of transcription | Q33945461 | ||
A synthetic A tail rescues yeast nuclear accumulation of a ribozyme-terminated transcript | Q33983114 | ||
Coupling of termination, 3' processing, and mRNA export | Q34325429 | ||
Pre-mRNA processing factors are required for nuclear export | Q34363202 | ||
T7 RNA polymerase-directed transcripts are processed in yeast and link 3' end formation to mRNA nuclear export | Q34364453 | ||
Localization of nuclear retained mRNAs in Saccharomyces cerevisiae | Q34365269 | ||
Rules of engagement: co-transcriptional recruitment of pre-mRNA processing factors | Q34419716 | ||
The role of Rat1 in coupling mRNA 3'-end processing to transcription termination: implications for a unified allosteric-torpedo model | Q34511126 | ||
Ubiquitin-associated domain of Mex67 synchronizes recruitment of the mRNA export machinery with transcription | Q35133832 | ||
The transcriptional cycle of HIV-1 in real-time and live cells. | Q36119592 | ||
Connections between mRNA 3' end processing and transcription termination | Q36131487 | ||
PCF11 encodes a third protein component of yeast cleavage and polyadenylation factor I. | Q36565604 | ||
The nuclear envelope and transcriptional control. | Q36840615 | ||
Functional significance of the interaction between the mRNA-binding protein, Nab2, and the nuclear pore-associated protein, Mlp1, in mRNA export | Q36914437 | ||
Protein factors in pre-mRNA 3'-end processing. | Q37044967 | ||
Regulation of mRNP dynamics along the export pathway | Q37131104 | ||
Biogenesis of mRNPs: integrating different processes in the eukaryotic nucleus | Q37144184 | ||
mRNA journey to the cytoplasm: attire required | Q37163404 | ||
Quality control of mRNP in the nucleus | Q37194592 | ||
mRNA nuclear export at a glance | Q37506920 | ||
Rna15 interaction with the A-rich yeast polyadenylation signal is an essential step in mRNA 3'-end formation | Q39529058 | ||
The yeast HPR1 gene has a functional role in transcriptional elongation that uncovers a novel source of genome instability | Q40444246 | ||
Separation of factors required for cleavage and polyadenylation of yeast pre-mRNA | Q40655774 | ||
Inefficient processing impairs release of RNA from the site of transcription | Q40954153 | ||
Biochemical analysis of TREX complex recruitment to intronless and intron-containing yeast genes | Q41062668 | ||
Cotranscriptional recruitment of the mRNA export factor Yra1 by direct interaction with the 3' end processing factor Pcf11. | Q41920187 | ||
Role of poly (A) tail as an identity element for mRNA nuclear export | Q43042769 | ||
Defects in the mRNA export factors Rat7p, Gle1p, Mex67p, and Rat8p cause hyperadenylation during 3'-end formation of nascent transcripts | Q43206826 | ||
The DEAD-box protein Dbp5p is required to dissociate Mex67p from exported mRNPs at the nuclear rim. | Q46093228 | ||
The DEAD-box protein Dbp5 controls mRNA export by triggering specific RNA:protein remodeling events | Q46848532 | ||
Elongator interactions with nascent mRNA revealed by RNA immunoprecipitation | Q47587838 | ||
THO/Sub2p functions to coordinate 3'-end processing with gene-nuclear pore association. | Q50336097 | ||
Regulation of yeast mRNA 3' end processing by phosphorylation. | Q53658895 | ||
Yeast mRNA Poly(A) tail length control can be reconstituted in vitro in the absence of Pab1p-dependent Poly(A) nuclease activity. | Q53675884 | ||
P433 | issue | 19 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 5327-5338 | |
P577 | publication date | 2009-07-27 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | Assembly of an export-competent mRNP is needed for efficient release of the 3'-end processing complex after polyadenylation | |
P478 | volume | 29 |
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