A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Reference Report

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Citation Sigrist, S.J., Thiel, P.R., Reiff, D.F., Lachance, P.E.D., Lasko, P., Schuster, C.M. (2000). Postsynaptic translation affects the efficacy and morphology of neuromuscular junctions.  Nature 405(6790): 1062--1065.
FlyBase ID FBrf0128816
Type of publication Research paper
Offprint Available Yes
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PubMed ID 10890448
PubMed Abstract Long-term synaptic plasticity may be associated with structural rearrangements within the neuronal circuitry. Although the molecular mechanisms governing such activity-controlled morphological alterations are mostly elusive, polysomal accumulations at the base of developing dendritic spines and the activity-induced synthesis of synaptic components suggest that localized translation is involved during synaptic plasticity. Here we show that large aggregates of translational components as well as messenger RNA of the postsynaptic glutamate receptor subunit DGluR-IIA are localized within subsynaptic compartments of larval neuromuscular junctions of Drosophila melanogaster. Genetic models of junctional plasticity and genetic manipulations using the translation initiation factors eIF4E and poly(A)-binding protein showed an increased occurrence of subsynaptic translation aggregates. This was associated with a significant increase in the postsynaptic DGluR-IIA protein levels and a reduction in the junctional expression of the cell-adhesion molecule Fasciclin II. In addition, the efficacy of junctional neurotransmission and the size of larval neuromuscular junctions were significantly increased. Our results therefore provide evidence for a postsynaptic translational control of long-term junctional plasticity.
Biosis 2000.404099
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Language of publication English
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Abbreviation Nature
Title Nature
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Volume range 1-
Year range 1869-
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Place of publication London
Language of publication English
ISBN/ISSN 0028-0836
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