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Originally published In Press as doi:10.1074/jbc.M008290200 on December 5, 2000

J. Biol. Chem., Vol. 276, Issue 12, 9133-9140, March 23, 2001
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The C-terminal Tail of the Metabotropic Glutamate Receptor Subtype 7 Is Necessary but Not Sufficient for Cell Surface Delivery and Polarized Targeting in Neurons and Epithelia*

J. Brian McCarthyDagger §, Seung T. Lim, N. Barry Elkind||, James S. Trimmer, Robert M. Duvoisin**, Enrique Rodriguez-Boulan**, and Michael J. CaplanDagger

From the Departments of Dagger  Cellular and Molecular Physiology and || Cell Biology, Yale University School of Medicine, New Haven, Connecticut 06520, the  Department of Biochemistry and Cell Biology and Institute for Cell and Developmental Biology, State University of New York at Stony Brook, Stony Brook, New York 11794-5215, and the ** Dyson Vision Research Institute, Departments of Ophthalmology and Cell Biology, Weill Medical College, Cornell University, New York, New York 10021

Complex neuronal functions rely upon the precise sorting, targeting, and restriction of receptors to specific synaptic microdomains. Little is known, however, of the molecular signals responsible for mediating these selective distributions. Here we report that metabotropic glutamate receptor subtype 7a (mGluR7a) is polarized at the basolateral surface when expressed in Madin-Darby canine kidney (MDCK) epithelial cells but is not polarized when expressed in cultured hippocampal neurons. Truncation of the mGluR7 cytoplasmic tail produces a protein that is restricted to a perinuclear intracellular compartment in both neurons and MDCK cells, where this protein colocalizes with a trans-Golgi network antigen. The mGluR7 cytoplasmic domain appended to the transmembrane portion of the vesicular stomatitis virus G protein and the ectodomain of human placental alkaline phosphatase is distributed over the entire cell surface in cultured neurons. When expressed in MDCK cells, this construct remains in an intracellular compartment distinct from endosomes or lysosomes. Thus, the cytoplasmic tail domain of mGluR7 is necessary but not sufficient for polarized targeting in MDCK monolayers, whereas in neurons the cytoplasmic tail is sufficient for cell surface expression but not polarization. Additional mechanisms are likely required to mediate mGluR7 neuronal polarization and synaptic clustering.


* This work was supported by National Institutes of Health Grant GM42136 and National Eye Institute Grant EY09534.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

§ To whom correspondence should be addressed. Tel.: 212-570-2900; Fax: 212-988-3672; E-mail: jbm2001@med.cornell.edu.


Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.
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