Abstract
Group III metabotropic glutamate receptors (mGluRs) are highly enriched in the presynaptic terminals of glutamatergic synapses where they mediate feedback inhibition of neurotransmitter release. Here, we used the yeast two-hybrid system to identify a direct interaction of the C-terminal tail region of mGluR7 with the rat homologue of the protein kinase C substrate PICK1. This interaction is specifically mediated by the very C-terminal amino acids of the receptor and can be reconstituted in human embryonic kidney 293 cells by transfection of full-length mGluR7 and PICK1 cDNAs. Quantitative beta-galactosidase assays revealed that among the different group III mGluRs, mGluR7 is the major PICK1 binding partner although other subfamily members can also interact with PICK1. These data indicate that PDZ domain-containing proteins might contribute to the presynaptic localization of group III mGluRs.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Binding Sites
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Caenorhabditis elegans
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Carrier Proteins / chemistry*
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Carrier Proteins / metabolism*
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Cell Cycle Proteins
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Cell Line
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Cloning, Molecular
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Cytoskeletal Proteins
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Humans
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Kidney
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Mice
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Molecular Sequence Data
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Nuclear Proteins / chemistry*
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Nuclear Proteins / metabolism*
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Peptide Fragments / chemistry
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Peptide Fragments / metabolism
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Rats
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Receptors, Metabotropic Glutamate / chemistry*
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Receptors, Metabotropic Glutamate / metabolism*
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Recombinant Fusion Proteins / metabolism
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Recombinant Proteins / chemistry
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Recombinant Proteins / metabolism
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Sequence Alignment
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Sequence Homology, Amino Acid
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Transfection
Substances
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Carrier Proteins
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Cell Cycle Proteins
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Cytoskeletal Proteins
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Nuclear Proteins
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PICK1 protein, rat
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PICk1 protein, human
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Peptide Fragments
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Prkcabp protein, mouse
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Receptors, Metabotropic Glutamate
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Recombinant Fusion Proteins
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Recombinant Proteins
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metabotropic glutamate receptor 7