Literature DB >> 11142374

Pre-mRNA processing factors are required for nuclear export.

A S Brodsky1, P A Silver.   

Abstract

RNA export from the nucleus is thought to be linked to proper processing and packaging into ribonucleoprotein protein complexes. A system to observe mRNA nuclear export in living yeast cells was developed by fusing the U1A RNA-binding protein to the green fluorescent protein to follow specific mRNAs with U1A hairpins engineered into them. RNAs encoding Rpl25, Pgk1, and Ssa4 were examined for the effects of 3' UTRs, introns, RNA processing factors, nucleoporins, and transport factors on their export. All accumulated in the nucleus in mutants affecting components of the nuclear export machinery and certain nucleoporins. However, under conditions of stress, PGK1 and RPL25 transcripts accumulate in the nucleus whereas SSA4 RNA is exported. Moreover, when export is blocked, only RNAs containing the ASH1 3' UTR accumulated in the nucleolus. Mutations in the splicing machinery selectively blocked export of only intron-containing RNAs. Mutations in RNA14, RNA15, and PAP1, which encode factors important for 3' processing, also blocked export of all RNAs, including SSA4, thereby linking export to the process of polyadenlyation. Taken together, these data graphically display the connections between mRNA processing and nuclear export.

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Year:  2000        PMID: 11142374      PMCID: PMC1370044          DOI: 10.1017/s1355838200001059

Source DB:  PubMed          Journal:  RNA        ISSN: 1355-8382            Impact factor:   4.942


  54 in total

1.  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.

Authors:  L Minvielle-Sebastia; B Winsor; N Bonneaud; F Lacroute
Journal:  Mol Cell Biol       Date:  1991-06       Impact factor: 4.272

2.  Isolation and characterization of RAT1: an essential gene of Saccharomyces cerevisiae required for the efficient nucleocytoplasmic trafficking of mRNA.

Authors:  D C Amberg; A L Goldstein; C N Cole
Journal:  Genes Dev       Date:  1992-07       Impact factor: 11.361

3.  Construction of a set of convenient Saccharomyces cerevisiae strains that are isogenic to S288C.

Authors:  F Winston; C Dollard; S L Ricupero-Hovasse
Journal:  Yeast       Date:  1995-01       Impact factor: 3.239

4.  Defects in mRNA 3'-end formation, transcription initiation, and mRNA transport associated with the yeast mutation prp20: possible coupling of mRNA processing and chromatin structure.

Authors:  W Forrester; F Stutz; M Rosbash; M Wickens
Journal:  Genes Dev       Date:  1992-10       Impact factor: 11.361

5.  Efficient translation of poly(A)-deficient mRNAs in Saccharomyces cerevisiae.

Authors:  A Proweller; S Butler
Journal:  Genes Dev       Date:  1994-11-01       Impact factor: 11.361

6.  Mature mRNA 3' end formation stimulates RNA export from the nucleus.

Authors:  R Eckner; W Ellmeier; M L Birnstiel
Journal:  EMBO J       Date:  1991-11       Impact factor: 11.598

7.  A new family of yeast nuclear pore complex proteins.

Authors:  S R Wente; M P Rout; G Blobel
Journal:  J Cell Biol       Date:  1992-11       Impact factor: 10.539

8.  Nuclear PRP20 protein is required for mRNA export.

Authors:  D C Amberg; M Fleischmann; I Stagljar; C N Cole; M Aebi
Journal:  EMBO J       Date:  1993-01       Impact factor: 11.598

9.  Isolation and characterization of Saccharomyces cerevisiae mRNA transport-defective (mtr) mutants.

Authors:  T Kadowaki; S Chen; M Hitomi; E Jacobs; C Kumagai; S Liang; R Schneiter; D Singleton; J Wisniewska; A M Tartakoff
Journal:  J Cell Biol       Date:  1994-08       Impact factor: 10.539

10.  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.

Authors:  L C Gorsch; T C Dockendorff; C N Cole
Journal:  J Cell Biol       Date:  1995-05       Impact factor: 10.539

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  84 in total

1.  A cis-acting element known to block 3' mRNA degradation enhances expression of polyA-minus mRNA in wild-type yeast cells and phenocopies a ski mutant.

Authors:  J T Brown; A W Johnson
Journal:  RNA       Date:  2001-11       Impact factor: 4.942

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.  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

4.  Defects in the mRNA export factors Rat7p, Gle1p, Mex67p, and Rat8p cause hyperadenylation during 3'-end formation of nascent transcripts.

Authors:  P Hilleren; R Parker
Journal:  RNA       Date:  2001-05       Impact factor: 4.942

5.  Evidence that poly(A) binding protein has an evolutionarily conserved function in facilitating mRNA biogenesis and export.

Authors:  Julia A Chekanova; Dmitry A Belostotsky
Journal:  RNA       Date:  2003-12       Impact factor: 4.942

6.  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

7.  A novel function for Sam68: enhancement of HIV-1 RNA 3' end processing.

Authors:  Meredith McLaren; Kengo Asai; Alan Cochrane
Journal:  RNA       Date:  2004-07       Impact factor: 4.942

8.  R-loop-mediated genome instability in mRNA cleavage and polyadenylation mutants.

Authors:  Peter C Stirling; Yujia A Chan; Sean W Minaker; Maria J Aristizabal; Irene Barrett; Payal Sipahimalani; Michael S Kobor; Philip Hieter
Journal:  Genes Dev       Date:  2012-01-15       Impact factor: 11.361

9.  Nuclear Pnn/DRS protein binds to spliced mRNPs and participates in mRNA processing and export via interaction with RNPS1.

Authors:  Chin Li; Ru-Inn Lin; Ming-Chih Lai; Pin Ouyang; Woan-Yuh Tarn
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

10.  Nuclear transit of the RNA-binding protein She2 is required for translational control of localized ASH1 mRNA.

Authors:  Tung-Gia Du; Stephan Jellbauer; Marisa Müller; Maria Schmid; Dierk Niessing; Ralf-Peter Jansen
Journal:  EMBO Rep       Date:  2008-06-20       Impact factor: 8.807

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