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The Journal of Neuroscience, August 1, 2002, 22(15):6471-6479
Regulation of Synaptic Plasticity and Synaptic Vesicle Dynamics
by the PDZ Protein Scribble
John P.
Roche*,
Mary C.
Packard*,
Stephanie
Moeckel-Cole, and
Vivian
Budnik
Department of Biology, Molecular and Cellular Biology Program,
University of Massachusetts, Amherst, Massachusetts 01003
The Drosophila tumor suppressor Scribble (Scrib) is
a PDZ-containing protein required for maintaining epithelial
cell polarity. At the larval neuromuscular junction, Scrib colocalizes
and indirectly interacts with another tumor suppressor and PDZ protein,
Discs-Large (Dlg). Previous studies demonstrate that Dlg is critical
for development of normal synapse structure and function, as well as
for normal synaptic Scrib localization. Here we show that Scrib is also
an important regulator of synaptic architecture and physiology. The most notable ultrastructural defect in scrib mutants is
an increase in the number of synaptic vesicles in an area of the
synaptic bouton thought to contain the reserve vesicle pool.
Additionally, the number of active zones is reduced in
scrib mutants. Functionally, the scrib
synapse behaves relatively normally at low-frequency stimulation.
However, several forms of plasticity at this synapse are drastically
altered in the mutants. Specifically, scrib mutants exhibit loss of facilitation and post-tetanic potentiation, and faster
synaptic depression. In addition, FM1-43 imaging of recycling synaptic
vesicles shows that vesicle dynamics are impaired in scrib mutants. These results identify Scrib as an
essential regulator of short-term synaptic plasticity. Taken together,
our results are consistent with a model in which Scrib is required to
sustain synaptic vesicle concentrations at their sites of release.
Key words:
Drosophila; synapse; facilitation; PTP; vesicle recycling; scribble; PDZ; Dlg; FM1-43; calcium; Guk-holder
*
J.P.R. and M.C.P. contributed equally to this work.
Copyright © 2002 Society for Neuroscience 0270-6474/02/22156471-09$05.00/0
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