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The EJC Factor eIF4AIII Modulates Synaptic Strength and Neuronal Protein Expression

Authors :
Giorgi, Corinna
Yeo, Gene W.
Stone, Martha E.
Katz, Donald B.
Burge, Christopher
Turrigiano, Gina
Moore, Melissa J.
Source :
Cell. July 13, 2007, Vol. 130 Issue 1, p179, 13 p.
Publication Year :
2007

Abstract

To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.cell.2007.05.028 Byline: Corinna Giorgi (1), Gene W. Yeo (2), Martha E. Stone (3), Donald B. Katz (3), Christopher Burge (4), Gina Turrigiano (5), Melissa J. Moore (1) Abstract: Proper neuronal function and several forms of synaptic plasticity are highly dependent on precise control of mRNA translation, particularly in dendrites. We find that eIF4AIII, a core exon junction complex (EJC) component loaded onto mRNAs by pre-mRNA splicing, is associated with neuronal mRNA granules and dendritic mRNAs. eIF4AIII knockdown markedly increases both synaptic strength and GLUR1 AMPA receptor abundance at synapses. eIF4AIII depletion also increases ARC, a protein required for maintenance of long-term potentiation; arc mRNA, one of the most abundant in dendrites, is a natural target for nonsense-mediated decay (NMD). Numerous new NMD candidates, some with potential to affect synaptic activity, were also identified computationally. Two models are presented for how translation-dependent decay pathways such as NMD might advantageously function as critical brakes for protein synthesis in cells such as neurons that are highly dependent on spatially and temporally restricted protein expression. Author Affiliation: (1) Department of Biochemistry, Howard Hughes Medical Institute, Brandeis University, Waltham, MA 02454, USA (2) Crick-Jacobs Center for Computational and Theoretical Biology Salk Institute, La Jolla, CA 92037, USA (3) Department of Psychology and Volen Center for Complex Systems, Brandeis University, Waltham, MA 02454, USA (4) Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA (5) Department of Biology and Volen Center for Complex Systems, Brandeis University, Waltham, MA 02454, USA Article History: Received 12 July 2006; Revised 23 December 2006; Accepted 9 May 2007 Article Note: (miscellaneous) Published: July 12, 2007

Subjects

Subjects :
Neurons
Biological sciences

Details

Language :
English
ISSN :
00928674
Volume :
130
Issue :
1
Database :
Gale General OneFile
Journal :
Cell
Publication Type :
Academic Journal
Accession number :
edsgcl.166446417