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NRAP-1 Is a Presynaptically Released NMDA Receptor Auxiliary Protein that Modifies Synaptic Strength.
- Source :
-
Neuron [Neuron] 2017 Dec 20; Vol. 96 (6), pp. 1303-1316.e6. Date of Electronic Publication: 2017 Dec 07. - Publication Year :
- 2017
-
Abstract
- NMDA receptors (NMDARs) are a subtype of postsynaptic ionotropic glutamate receptors that function as molecular coincidence detectors, have critical roles in models of learning, and are associated with a variety of neurological and psychiatric disorders. To date, no auxiliary proteins that modify NMDARs have been identified. Here, we report the identification of NRAP-1, an auxiliary protein in C. elegans that modulates NMDAR function. NMDAR-mediated currents were eliminated in nrap-1 mutants, as was NMDA-dependent behavior. We show that reconstitution of NMDA-gated current in Xenopus oocytes, or C. elegans muscle cells, depends on NRAP-1 and that recombinant NRAP-1 can convert silent NMDARs to functional channels. Our data indicate that NRAP-1, secreted from presynaptic neurons, localizes to glutamatergic synapses, where it associates with postsynaptic NMDARs to modify receptor gating. Thus, our studies reveal a novel mechanism for synaptic regulation via pre-synaptic control of NMDAR-mediated synaptic transmission.<br /> (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Animals, Genetically Modified
Caenorhabditis elegans
Caenorhabditis elegans Proteins genetics
Gene Expression Regulation genetics
Glutamic Acid pharmacology
Interneurons drug effects
Ion Channel Gating drug effects
Ion Channel Gating genetics
Membrane Proteins drug effects
Movement drug effects
Muscle Cells cytology
Muscle Cells drug effects
Mutation genetics
N-Methylaspartate pharmacology
Nuclear Proteins genetics
Oocytes
RNA-Binding Proteins
Receptors, N-Methyl-D-Aspartate genetics
Recombinant Proteins genetics
Recombinant Proteins metabolism
Signal Transduction drug effects
Signal Transduction genetics
Synapses drug effects
Synapses genetics
Xenopus
Caenorhabditis elegans Proteins metabolism
Interneurons cytology
Membrane Proteins genetics
Movement physiology
Nuclear Proteins metabolism
Receptors, N-Methyl-D-Aspartate metabolism
Synapses physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4199
- Volume :
- 96
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Neuron
- Publication Type :
- Academic Journal
- Accession number :
- 29224722
- Full Text :
- https://doi.org/10.1016/j.neuron.2017.11.019