| The brain is an extremely complex
circuit. For example, a single neuron can receive over 10,000 synaptic
inputs and express multiple neurotransmitter receptor types that
must be segregated to appropriate synaptic sites. While complex,
the nervous system also must remain malleable. Understanding how
the nervous system forms synapses and regulates their composition
is key to understanding the basis for learning and memory.
Our work is focused on two primary questions. First, how are different
receptor types sorted to the appropriate synapses in a neuron? Second,
how do synapses in the central nervous system change in the growing
animal? We have taken advantage of the simple anatomy and well-characterized
genetics of C. elegans to address these questions. By using genetic
screens, behavioral analysis, and molecular and cell biological
techniques in living animals, we hope to identify the proteins that
build and regulate synapses. |
| For complete list: PubMed
Rongo, C. (2002) A fresh look at the role of CaM
Kinase II in hippocampal synaptic plasticity and memory. BioEssays
24:223-233.
Firestein, B.L. and Rongo, C. (2001) DLG-1 is
a MAGUK similar to SAP97 and is required for adherens junction formation.
Molecular Biology of the Cell: 12:3465-3475.
Köppen, M., Simske, J., Sims, P., Firestein, B., Hall,
D., Radice, G., Rongo, C., and Hardin, J. (2001) Cooperative
regulation of JAM-1 by DLG-1 and LET-413 controls junctional tightness
of C. elegans epithelia. Nature Cell Biology 3:983-991.
Rongo, C. (2001) Disparate cell types use a shared
complex of PDZ proteins for polarized protein localization. Cytokine
& Growth Factor Reviews 12:349-359.
Rongo, C. and Kaplan, J.M. (1999) CaMKII regulates
the density of central glutamatergic synapses in vivo. Nature
402:195-199.
Rongo, C., Whitfield, C.W., Rodal, A., Kim, S.K., and Kaplan,
J.M. (1998) LIN-10 is a shared component of the polarized
protein localization pathways in neurons and epithelia. Cell
94:751-759.
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