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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