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Moesin helps to restrain synaptic growth at the Drosophila neuromuscular junction
Author(s) -
Seabrooke Sara,
Stewart Bryan A.
Publication year - 2007
Publication title -
developmental neurobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.716
H-Index - 129
eISSN - 1932-846X
pISSN - 1932-8451
DOI - 10.1002/dneu.20595
Subject(s) - moesin , biology , neuromuscular junction , microbiology and biotechnology , phenotype , excitatory postsynaptic potential , synapse , actin , neuroscience , cytoskeleton , genetics , inhibitory postsynaptic potential , cell , gene , ezrin
The precise role of actin and actin‐binding proteins in synaptic development is unclear. In Drosophila , overexpression of a dominant‐negative NSF2 construct perturbs filamentous actin, which is associated with overgrowth of the NMJ, while co‐expression of moesin , which encodes an actin binding protein, suppresses this overgrowth phenotype. These data suggest that Moesin may play a role in synaptic development at the Drosophila NMJ. To further investigate this possibility, we examined the influence of loss‐of‐function moesin alleles on the NSF2 ‐induced overgrowth phenotype. We found that flies carrying P‐element insertions that reduce moesin expression enhanced the NMJ overgrowth phenotype, indicating a role for Moesin in normal NMJ morphology. In addition to the NMJ overgrowth phenotype, expression of dominant‐negative NSF2 is known to reduce the frequency of miniature excitatory junctional potentials and the amplitude of excitatory junctional potentials. We found that moesin coexpression did not restore the physiology of the mutant NSF2 phenotype. Together, our results demonstrate a role for moesin in regulating synaptic growth in the Drosophila NMJ and suggest that the effect of dominant‐negative NSF2 on NMJ morphology and physiology may have different underlying molecular origins. © 2007 Wiley Periodicals, Inc. Develop Neurobiol, 2008.