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Biobehavioral Seminar Series

Mark Bear, Ph.D.Date: May 5, 2006

Time: Noon to 1:30

Title: The mGluR Theory of Fragile X Mental Retardation

Speaker: Mark F. Bear, Ph.D.  
Massachusetts Institute of Technology

Where: Waisman Conference Center
Room T216, Second Floor, North Tower

For Further Information: Contact Teresa Palumbo at 263-5837 or
palumbo@waisman.wisc.edu

About the Talk:
Many of the diverse functional consequences of activating group 1 metabotropic glutamate receptors require translation of pre-existing mRNA near synapses. One of these consequences is long-term depression (LTD) of transmission at hippocampal synapses. Loss of fragile X mental retardation protein (FMRP), the defect responsible for fragile X syndrome in humans, increases LTD in mouse hippocampus. This finding is consistent with the growing evidence that FMRP normally functions as a repressor of translation of specific mRNAs. Here we present a theory that can account for diverse neurological and psychiatric aspects of fragile X syndrome, based on the assumption that many of the protein synthesis dependent functions of metabotropic receptors are exaggerated in fragile X syndrome. The theory suggests new directions for basic research as well as novel therapeutic approaches for the treatment of humans with fragile X, the most frequent inherited cause of mental retardation and an identified cause of autism.

 

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