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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
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
McCarthy §,
Seung T.
Lim¶,
N. Barry
Elkind ,
James S.
Trimmer¶,
Robert M.
Duvoisin**,
Enrique
Rodriguez-Boulan**, and
Michael J.
Caplan
From the Departments of 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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Copyright © 2001 by the American Society for Biochemistry and Molecular Biology.
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