eIF4AIII binds spliced mRNA in the exon junction complex and is essential for nonsense-mediated decay
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Shibuya, T
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机构:Brandeis Univ, Dept Biochem, Howard Hughes Med Inst, Waltham, MA 02454 USA
Shibuya, T
Tange, TO
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机构:Brandeis Univ, Dept Biochem, Howard Hughes Med Inst, Waltham, MA 02454 USA
Tange, TO
Sonenberg, N
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机构:Brandeis Univ, Dept Biochem, Howard Hughes Med Inst, Waltham, MA 02454 USA
Sonenberg, N
Moore, MJ
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Brandeis Univ, Dept Biochem, Howard Hughes Med Inst, Waltham, MA 02454 USABrandeis Univ, Dept Biochem, Howard Hughes Med Inst, Waltham, MA 02454 USA
Moore, MJ
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[1] Brandeis Univ, Dept Biochem, Howard Hughes Med Inst, Waltham, MA 02454 USA
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.