Literature DB >> 11459827

Messenger RNAs are recruited for nuclear export during transcription.

E P Lei1, H Krebber, P A Silver.   

Abstract

Following transcription and processing, eukaryotic mRNAs are exported from the nucleus to the cytoplasm for translation. Here we present evidence that mRNAs are targeted for nuclear export cotranscriptionally. Combined mutations in the Saccharomyces cerevisiae hnRNP Npl3 and TATA-binding protein (TBP) block mRNA export, implying that cotranscriptional recruitment of Npl3 is required for efficient export of mRNA. Furthermore, Npl3 can be found in a complex with RNA Pol II, indicating that Npl3 associates with the transcription machinery. Finally, Npl3 is recruited to genes in a transcription dependent manner as determined by chromatin immunoprecipitation. Another mRNA export factor, Yra1, also associates with chromatin cotranscriptionally but appears to be recruited at a later step. Taken together, our results suggest that export factors are recruited to the sites of transcription to promote efficient mRNA export.

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Year:  2001        PMID: 11459827      PMCID: PMC312744          DOI: 10.1101/gad.892401

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  61 in total

1.  The Spt components of SAGA facilitate TBP binding to a promoter at a post-activator-binding step in vivo.

Authors:  A M Dudley; C Rougeulle; F Winston
Journal:  Genes Dev       Date:  1999-11-15       Impact factor: 11.361

2.  Yra1p, a conserved nuclear RNA-binding protein, interacts directly with Mex67p and is required for mRNA export.

Authors:  K Strässer; E Hurt
Journal:  EMBO J       Date:  2000-02-01       Impact factor: 11.598

Review 3.  RNA polymerase II and the integration of nuclear events.

Authors:  Y Hirose; J L Manley
Journal:  Genes Dev       Date:  2000-06-15       Impact factor: 11.361

4.  Splicing is required for rapid and efficient mRNA export in metazoans.

Authors:  M J Luo; R Reed
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

5.  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.

Authors:  Y Strahm; B Fahrenkrog; D Zenklusen; E Rychner; J Kantor; M Rosbach; F Stutz
Journal:  EMBO J       Date:  1999-10-15       Impact factor: 11.598

6.  Characterization of the ptr6(+) gene in fission yeast: a possible involvement of a transcriptional coactivator TAF in nucleocytoplasmic transport of mRNA.

Authors:  T Shibuya; S Tsuneyoshi; A K Azad; S Urushiyama; Y Ohshima; T Tani
Journal:  Genetics       Date:  1999-07       Impact factor: 4.562

7.  Uncoupling of the hnRNP Npl3p from mRNAs during the stress-induced block in mRNA export.

Authors:  H Krebber; T Taura; M S Lee; P A Silver
Journal:  Genes Dev       Date:  1999-08-01       Impact factor: 11.361

8.  The C-terminal domain of TAP interacts with the nuclear pore complex and promotes export of specific CTE-bearing RNA substrates.

Authors:  A Bachi; I C Braun; J P Rodrigues; N Panté; K Ribbeck; C von Kobbe; U Kutay; M Wilm; D Görlich; M Carmo-Fonseca; E Izaurralde
Journal:  RNA       Date:  2000-01       Impact factor: 4.942

9.  The yeast hnRNP-like protein Hrp1/Nab4 marks a transcript for nonsense-mediated mRNA decay.

Authors:  C I González; M J Ruiz-Echevarría; S Vasudevan; M F Henry; S W Peltz
Journal:  Mol Cell       Date:  2000-03       Impact factor: 17.970

10.  A yeast RNA-binding protein shuttles between the nucleus and the cytoplasm.

Authors:  J Flach; M Bossie; J Vogel; A Corbett; T Jinks; D A Willins; P A Silver
Journal:  Mol Cell Biol       Date:  1994-12       Impact factor: 4.272

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  110 in total

1.  Trans-splicing as a novel mechanism to explain interallelic complementation in Drosophila.

Authors:  Fabien Mongelard; Mariano Labrador; Ellen M Baxter; Tatiana I Gerasimova; Victor G Corces
Journal:  Genetics       Date:  2002-04       Impact factor: 4.562

2.  T7 RNA polymerase-directed transcripts are processed in yeast and link 3' end formation to mRNA nuclear export.

Authors:  Ken Dower; Michael Rosbash
Journal:  RNA       Date:  2002-05       Impact factor: 4.942

3.  Regulation of transcription by the heterogeneous nuclear ribonucleoprotein E1B-AP5 is mediated by complex formation with the novel bromodomain-containing protein BRD7.

Authors:  Julia Kzhyshkowska; Andre Rusch; Hans Wolf; Thomas Dobner
Journal:  Biochem J       Date:  2003-04-15       Impact factor: 3.857

4.  Intron status and 3'-end formation control cotranscriptional export of mRNA.

Authors:  Elissa P Lei; Pamela A Silver
Journal:  Genes Dev       Date:  2002-11-01       Impact factor: 11.361

5.  The mRNA export machinery requires the novel Sac3p-Thp1p complex to dock at the nucleoplasmic entrance of the nuclear pores.

Authors:  Tamás Fischer; Katja Strässer; Attila Rácz; Susana Rodriguez-Navarro; Marisa Oppizzi; Petra Ihrig; Johannes Lechner; Ed Hurt
Journal:  EMBO J       Date:  2002-11-01       Impact factor: 11.598

6.  ICP27 selectively regulates the cytoplasmic localization of a subset of viral transcripts in herpes simplex virus type 1-infected cells.

Authors:  Angela Pearson; David M Knipe; Donald M Coen
Journal:  J Virol       Date:  2004-01       Impact factor: 5.103

7.  Cotranscriptional recruitment of the serine-arginine-rich (SR)-like proteins Gbp2 and Hrb1 to nascent mRNA via the TREX complex.

Authors:  Ed Hurt; Ming-Juan Luo; Susanne Röther; Robin Reed; Katja Strässer
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-09       Impact factor: 11.205

8.  Rpb4p, a subunit of RNA polymerase II, mediates mRNA export during stress.

Authors:  Marganit Farago; Tal Nahari; Christopher Hammel; Charles N Cole; Mordechai Choder
Journal:  Mol Biol Cell       Date:  2003-07       Impact factor: 4.138

9.  Perturbation of transcription elongation influences the fidelity of internal exon inclusion in Saccharomyces cerevisiae.

Authors:  Kenneth James Howe; Caroline M Kane; Manuel Ares
Journal:  RNA       Date:  2003-08       Impact factor: 4.942

10.  Rds3p is required for stable U2 snRNP recruitment to the splicing apparatus.

Authors:  Qiang Wang; Brian C Rymond
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

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