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Association of the Small GTPase Rheb with the NMDA Receptor Subunit NR3ASucher N.J.a–c · Yu E.d · Chan S.F.d · Miri M.b · Lee B.J.b · Xiao B.e · Worley P.F.e · Jensen F.E.b, c, f
aCentre for Complementary Medicine Research, University of Western Sydney, Penrith South DC, N.S.W., Australia; bDepartment of Neurology, Division of Neuroscience, Children’s Hospital, and cDepartment of Neurology, Harvard Medical School, Boston, Mass., dSanford-Burnham Medical Research Institute, La Jolla, Calif. eDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Md., and fProgram in Neuroscience, Harvard Medical School, Boston, Mass., USA Corresponding Author
Prof. Nikolaus J. Sucher
The Centre for Complementary Medicine Research
University of Western Sydney, Locked Bag 1797
Penrith, NSW 2751 (Australia)
Tel. +61 2 4620 3345, Fax +61 2 4620 3017, E-Mail firstname.lastname@example.org
The NMDAR subunit NR3A is most highly expressed during the second postnatal week, when synaptogenesis reaches peak levels. Genetic ablation or overexpression of the NR3A subunit negatively interferes with the maturation of cortical synapses and leads to changes in the shape and number of dendritic spines, the density of which is increased in NR3A knock-out mice and decreased in NR3A-overexpressing transgenic mice. Alterations in spine density have been linked to dysregulation of mTOR signaling and synaptic protein translation. Using a yeast two-hybrid system, we identified the mTOR-activating GTPase Rheb as an interacting protein of the NMDAR subunit NR3A. We confirmed the interaction in mammalian cells by expressing recombinant Rheb and NR3A and showed that Rheb and NR3A could be co-immunoprecipitated from synaptic plasma membranes from the developing rat brain. These data suggest that NR3A sequesters synaptic Rheb and might thus function as a break of the mTOR-dependent synaptic translation of protein.
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