scholarly article | Q13442814 |
P50 | author | Hediye Erdjument-Bromage | Q25910537 |
Paul Tempst | Q25912123 | ||
Andrés Aguilera | Q37382275 | ||
P2093 | author name string | Rosa Luna | |
Mercedes Gallardo | |||
P2860 | cites work | TREX is a conserved complex coupling transcription with messenger RNA export | Q24295211 |
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Structural insights into ligand interactions at the acetylcholinesterase peripheral anionic site | Q27640254 | ||
A generic protein purification method for protein complex characterization and proteome exploration | Q27861087 | ||
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 | ||
RNA polymerase II targets pre-mRNA splicing factors to transcription sites in vivo | Q77962891 | ||
Stable mRNP formation and export require cotranscriptional recruitment of the mRNA export factors Yra1p and Sub2p by Hpr1p | Q27929754 | ||
Sac3 is an mRNA export factor that localizes to cytoplasmic fibrils of nuclear pore complex | Q27930275 | ||
Nab2p is required for poly(A) RNA export in Saccharomyces cerevisiae and is regulated by arginine methylation via Hmt1p | Q27931019 | ||
Binding of the Mex67p/Mtr2p heterodimer to FXFG, GLFG, and FG repeat nucleoporins is essential for nuclear mRNA export. | Q27931219 | ||
The mRNA export machinery requires the novel Sac3p-Thp1p complex to dock at the nucleoplasmic entrance of the nuclear pores | Q27931766 | ||
The C-terminal domain of myosin-like protein 1 (Mlp1p) is a docking site for heterogeneous nuclear ribonucleoproteins that are required for mRNA export | Q27932831 | ||
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 | ||
NAB2: a yeast nuclear polyadenylated RNA-binding protein essential for cell viability | Q27934906 | ||
A novel yeast gene, THO2, is involved in RNA pol II transcription and provides new evidence for transcriptional elongation-associated recombination. | Q27936954 | ||
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 | ||
Mex67p, a novel factor for nuclear mRNA export, binds to both poly(A)+ RNA and nuclear pores | Q27940054 | ||
SAC3 may link nuclear protein export to cell cycle progression | Q27940254 | ||
The C-terminal domain of RNA polymerase II couples mRNA processing to transcription | Q28301744 | ||
The C-terminal domain of the largest subunit of RNA polymerase II interacts with a novel set of serine/arginine-rich proteins | Q28570708 | ||
Integrating mRNA processing with transcription | Q28610124 | ||
Isolation and characterization of RAT1: an essential gene of Saccharomyces cerevisiae required for the efficient nucleocytoplasmic trafficking of mRNA | Q29620080 | ||
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Recombinational repair in yeast: functional interactions between Rad51 and Rad54 proteins. | Q33886585 | ||
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A conserved mRNA export machinery coupled to pre-mRNA splicing | Q34120025 | ||
Nuclear export of mRNA. | Q34286048 | ||
Coupling of termination, 3' processing, and mRNA export | Q34325429 | ||
The nuclear matrix protein p255 is a highly phosphorylated form of RNA polymerase II largest subunit which associates with spliceosomes | Q34620338 | ||
A multitude of suppressors of group II intron-splicing defects in yeast | Q36757121 | ||
A hyperphosphorylated form of the large subunit of RNA polymerase II is associated with splicing complexes and the nuclear matrix | Q37398137 | ||
High-copy-number expression of Sub2p, a member of the RNA helicase superfamily, suppresses hpr1-mediated genomic instability | Q39460646 | ||
The yeast HPR1 gene has a functional role in transcriptional elongation that uncovers a novel source of genome instability | Q40444246 | ||
Nuclear export signals and the fast track to the cytoplasm | Q40459787 | ||
Inefficient processing impairs release of RNA from the site of transcription | Q40954153 | ||
Pre-mRNA processing and the CTD of RNA polymerase II: the tail that wags the dog? | Q41478723 | ||
Recombination between DNA repeats in yeast hpr1delta cells is linked to transcription elongation | Q41950317 | ||
Coupling termination of transcription to messenger RNA maturation in yeast. | Q52529973 | ||
P433 | issue | 26 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell biology | Q7141 |
Thp1p YOL072W | Q27547384 | ||
P304 | page(s) | 24225-32 | |
P577 | publication date | 2003-06-27 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | Nab2p and the Thp1p-Sac3p complex functionally interact at the interface between transcription and mRNA metabolism | |
P478 | volume | 278 |
Q27932638 | A genetic interaction map of RNA-processing factors reveals links between Sem1/Dss1-containing complexes and mRNA export and splicing |
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Q27931906 | A new connection of mRNP biogenesis and export with transcription-coupled repair |
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Q27939024 | A novel role for Sem1 and TREX-2 in transcription involves their impact on recruitment and H2B deubiquitylation activity of SAGA. |
Q54479973 | A pathway from leukemogenic oncogenes and stem cell chemokines to RNA processing via THOC5. |
Q90167023 | Actin and Nuclear Envelope Components Influence Ectopic Recombination in the Absence of Swr1 |
Q27931955 | An hpr1 point mutation that impairs transcription and mRNP biogenesis without increasing recombination. |
Q34807892 | Arabidopsis TRANSCURVATA1 encodes NUP58, a component of the nucleopore central channel |
Q35153726 | BRCA1 recruitment to transcriptional pause sites is required for R-loop-driven DNA damage repair |
Q50455260 | BRCA2 prevents R-loop accumulation and associates with TREX-2 mRNA export factor PCID2. |
Q37144184 | Biogenesis of mRNPs: integrating different processes in the eukaryotic nucleus |
Q33790486 | Comparative genomics of proteins involved in RNA nucleocytoplasmic export |
Q34267573 | Cotranscriptionally Formed DNA:RNA Hybrids Mediate Transcription Elongation Impairment and Transcription-Associated Recombination |
Q36294482 | Definition of global and transcript-specific mRNA export pathways in metazoans |
Q27936364 | Different physiological relevance of yeast THO/TREX subunits in gene expression and genome integrity |
Q90583385 | Distinct effects on mRNA export factor GANP underlie neurological disease phenotypes and alter gene expression depending on intron content |
Q42831302 | Evidence that the Arabidopsis Ubiquitin C-terminal Hydrolases 1 and 2 associate with the 26S proteasome and the TREX-2 complex |
Q28245155 | Exporting RNA from the nucleus to the cytoplasm |
Q41952528 | Falling for the dark side of transcription: Nab2 fosters RNA polymerase III transcription |
Q27677076 | Functional and structural characterization of the mammalian TREX-2 complex that links transcription with nuclear messenger RNA export |
Q36801218 | GANP protein encoded on human chromosome 21/mouse chromosome 10 is associated with resistance to mammary tumor development. |
Q36906733 | GANP regulates recruitment of AID to immunoglobulin variable regions by modulating transcription and nucleosome occupancy |
Q42824085 | GANP suppresses DNA recombination, measured by direct-repeat beta-galactosidase gene construct, but does not suppress the type of recombination applying to immunoglobulin genes in mammalian cells |
Q34025211 | GANP-mediated recruitment of activation-induced cytidine deaminase to cell nuclei and to immunoglobulin variable region DNA. |
Q27932821 | General, rapid, and transcription-dependent fragmentation of nucleolar antigens in S. cerevisiae mRNA export mutants |
Q28266306 | Genome instability: a mechanistic view of its causes and consequences |
Q34415765 | Genome-wide profiling of yeast DNA:RNA hybrid prone sites with DRIP-chip |
Q39551929 | Identification of mRNAs that are spliced but not exported to the cytoplasm in the absence of THOC5 in mouse embryo fibroblasts |
Q41941071 | Large-scale screening of yeast mutants for sensitivity to the IMP dehydrogenase inhibitor 6-azauracil |
Q33691010 | Mechanisms of genome instability induced by RNA-processing defects |
Q42060826 | Mediator and TREX-2: Emerging links between transcription initiation and mRNA export |
Q50336100 | Molecular evidence that the eukaryotic THO/TREX complex is required for efficient transcription elongation |
Q35133617 | Nab2 functions in the metabolism of RNA driven by polymerases II and III. |
Q27940185 | Nuclear export of the yeast mRNA-binding protein Nab2 is linked to a direct interaction with Gfd1 and to Gle1 function |
Q41037267 | Partial depletion of histone H4 increases homologous recombination-mediated genetic instability |
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Q42728158 | Retroviruses and yeast retrotransposons use overlapping sets of host genes |
Q39384335 | Selective cell death of p53-insufficient cancer cells is induced by knockdown of the mRNA export molecule GANP. |
Q37234377 | Sem1 is a functional component of the nuclear pore complex-associated messenger RNA export machinery |
Q34558162 | Sem1: a versatile "molecular glue"? |
Q27682989 | Structural basis for binding the TREX2 complex to nuclear pores, GAL1 localisation and mRNA export |
Q27677340 | Structural basis for the assembly and nucleic acid binding of the TREX-2 transcription-export complex |
Q42259082 | Structure of the Sac3 RNA-binding M-region in the Saccharomyces cerevisiae TREX-2 complex |
Q36942429 | Sus1 is recruited to coding regions and functions during transcription elongation in association with SAGA and TREX2. |
Q27934062 | Sus1, Sac3, and Thp1 mediate post-transcriptional tethering of active genes to the nuclear rim as well as to non-nascent mRNP. |
Q27937843 | Sus1, a functional component of the SAGA histone acetylase complex and the nuclear pore-associated mRNA export machinery |
Q38051409 | Sus1/ENY2: a multitasking protein in eukaryotic gene expression |
Q40596539 | The Nuclear Pore-Associated TREX-2 Complex Employs Mediator to Regulate Gene Expression |
Q24807183 | The PAM domain, a multi-protein complex-associated module with an all-alpha-helix fold |
Q40611665 | The Sac3 TPR-like region in the Saccharomyces cerevisiae TREX-2 complex is more extensive but independent of the CID region |
Q27939828 | The THP1-SAC3-SUS1-CDC31 complex works in transcription elongation-mRNA export preventing RNA-mediated genome instability. |
Q38205642 | The contribution of co-transcriptional RNA:DNA hybrid structures to DNA damage and genome instability |
Q27932704 | The mitogen-activated protein kinase Slt2 regulates nuclear retention of non-heat shock mRNAs during heat shock-induced stress |
Q27931954 | Tho1, a novel hnRNP, and Sub2 provide alternative pathways for mRNP biogenesis in yeast THO mutants |
Q57970965 | Transcription and mRNA export machineries SAGA and TREX-2 maintain monoubiquitinated H2B balance required for DNA repair |
Q27938676 | Yeast centrin Cdc31 is linked to the nuclear mRNA export machinery |
Q48164113 | mRNA export in the apicomplexan parasite Toxoplasma gondii: emerging divergent components of a crucial pathway |
Q37163404 | mRNA journey to the cytoplasm: attire required |