How does a single neuron establish and maintain many functionally distinct synapses? How are specific synaptic proteins added and removed from specific synapses to regulate signal transmission efficiency? Recent evidence suggests that changes in post-synaptic protein distribution constitute a cell biological mechanism leading to long term potentiation and long term depression, which are believed to form the basis of memory and learning. It was previously shown that a phylogenetically conserved PDZ-domain containing protein (LIN-10) is required for targeting of an AMPA-type glutamate receptor (GluR) to central synapses in C. elegans. This synaptic function of LIN- 10 is likely to be phylogenetically conserved since a human orthologue (X11/Mint) can functionally replace the endogenous worm protein. The goal of this proposal is to elucidate the mechanism by which LIN-10 regulates the abundance of GluR localization at post-synaptic elements as a step towards understanding the dynamic regulation of synaptic protein localization. A comparison with the function of LIN-10 in epithelial cells will test the hypothesis that a basic mechanism for protein localization is common in both cell types.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32NS041705-02
Application #
6540463
Study Section
Special Emphasis Panel (ZRG1-MDCN-1 (20))
Program Officer
Finkelstein, Robert
Project Start
2002-06-01
Project End
Budget Start
2002-06-01
Budget End
2002-07-31
Support Year
2
Fiscal Year
2002
Total Cost
$9,202
Indirect Cost
Name
University of California Berkeley
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
094878337
City
Berkeley
State
CA
Country
United States
Zip Code
94704