Literature DB >> 15034551

eIF4AIII binds spliced mRNA in the exon junction complex and is essential for nonsense-mediated decay.

Toshiharu Shibuya1, Thomas Ø Tange, Nahum Sonenberg, Melissa J Moore.   

Abstract

The exon junction complex (EJC), a set of proteins deposited on mRNAs as a consequence of pre-mRNA splicing, is a key effector of downstream mRNA metabolism. We have identified eIF4AIII, a member of the eukaryotic translation initiation factor 4A family of RNA helicases (also known as DExH/D box proteins), as a novel EJC core component. Crosslinking and antibody inhibition studies suggest that eIF4AIII constitutes at least part of the platform anchoring other EJC components to spliced mRNAs. A nucleocytoplasmic shuttling protein, eIF4AIII associates in vitro and in vivo with two other EJC core factors, Y14 and Magoh. In mammalian cells, eIF4AIII is essential for nonsense-mediated mRNA decay (NMD). Finally, a model is proposed by which eIF4AIII represents a new functional class of DExH/D box proteins that act as RNA clamps or 'place holders' for the sequence-independent attachment of additional factors to RNAs.

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Year:  2004        PMID: 15034551     DOI: 10.1038/nsmb750

Source DB:  PubMed          Journal:  Nat Struct Mol Biol        ISSN: 1545-9985            Impact factor:   15.369


  112 in total

1.  Nonsense-mediated decay does not occur within the yeast nucleus.

Authors:  Nicolas Kuperwasser; Saverio Brogna; Ken Dower; Michael Rosbash
Journal:  RNA       Date:  2004-12       Impact factor: 4.942

2.  The nonsense-mediated decay pathway maintains synapse architecture and synaptic vesicle cycle efficacy.

Authors:  A Ashleigh Long; Cecon T Mahapatra; Elvin A Woodruff; Jeff Rohrbough; Hung-Tat Leung; Shikoh Shino; Lingling An; Rebecca W Doerge; Mark M Metzstein; William L Pak; Kendal Broadie
Journal:  J Cell Sci       Date:  2010-09-07       Impact factor: 5.285

3.  Retention of spliceosomal components along ligated exons ensures efficient removal of multiple introns.

Authors:  Tara L Crabb; Bianca J Lam; Klemens J Hertel
Journal:  RNA       Date:  2010-07-07       Impact factor: 4.942

Review 4.  The exon junction complex as a node of post-transcriptional networks.

Authors:  Hervé Le Hir; Jérôme Saulière; Zhen Wang
Journal:  Nat Rev Mol Cell Biol       Date:  2015-12-16       Impact factor: 94.444

5.  RNA aptamers to mammalian initiation factor 4G inhibit cap-dependent translation by blocking the formation of initiation factor complexes.

Authors:  Shin Miyakawa; Akihiro Oguro; Takashi Ohtsu; Hiroaki Imataka; Nahum Sonenberg; Yoshikazu Nakamura
Journal:  RNA       Date:  2006-08-29       Impact factor: 4.942

6.  Splicing of U12-type introns deposits an exon junction complex competent to induce nonsense-mediated mRNA decay.

Authors:  Tetsuro Hirose; Mei-Di Shu; Joan A Steitz
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-17       Impact factor: 11.205

7.  Control of VP16 translation by the herpes simplex virus type 1 immediate-early protein ICP27.

Authors:  Kimberly S Ellison; Robert A Maranchuk; Kelly L Mottet; James R Smiley
Journal:  J Virol       Date:  2005-04       Impact factor: 5.103

8.  Biochemical analysis of the EJC reveals two new factors and a stable tetrameric protein core.

Authors:  Thomas Ø Tange; Toshiharu Shibuya; Melissa S Jurica; Melissa J Moore
Journal:  RNA       Date:  2005-12       Impact factor: 4.942

9.  The mammalian RNA-binding protein Staufen2 links nuclear and cytoplasmic RNA processing pathways in neurons.

Authors:  Michaela Monshausen; Niels H Gehring; Kenneth S Kosik
Journal:  Neuromolecular Med       Date:  2004       Impact factor: 3.843

10.  RIPiT-Seq: a high-throughput approach for footprinting RNA:protein complexes.

Authors:  Guramrit Singh; Emiliano P Ricci; Melissa J Moore
Journal:  Methods       Date:  2013-10-02       Impact factor: 3.608

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