Medical Journals

Unc-13 and Unc-10/Rim Localize Synaptic Vesicles to Specific Membrane Domains.

Authors:
  • Weimer Robby M
  • Gracheva Elena O
  • Meyrignac Olivier
  • Miller Kenneth G
  • Richmond Janet E
  • Bessereau Jean-Louis

From: Ecole Normale Supérieure, Biologie Cellulaire de la Synapse, and Institut National de la Santé et de la Recherche Médicale, U789, F-75005 Paris, France,.

The Journal of neuroscience : the official journal of the Society for Neuroscience

  • Publish Date: Aug 2006
  • ISSN: 1529-2401
  • Volume: 26
  • Issue: 31
  • Pages: 8040-7
  • Medium: Internet
  • Language: English
  • Citation (JAMA): Weimer Robby M, Gracheva Elena O, Meyrignac Olivier, et al. Unc-13 and Unc-10/Rim Localize Synaptic Vesicles to Specific Membrane Domains.. J. Neurosci. Aug 2006;26:8040-7

Abstract

Synaptic vesicles undergo a maturation step, termed priming, in which they become competent to fuse with the plasma membrane. To morphologically define the site of vesicle priming and identify fusion-competent synaptic vesicles, we combined a rapid physical-fixation technique with immunogold staining and high-resolution morphometric analysis at Caenorhabditis elegans neuromuscular junctions. In these presynaptic terminals, a subset of synaptic vesicles contact the plasma membrane within approximately 100 nm of a presynaptic dense projection. UNC-13, a protein required for vesicle priming, localizes to this same region of the plasma membrane. In an unc-13 null mutant, few synaptic vesicles contact the plasma membrane, suggesting that membrane-contacting synaptic vesicles represent the morphological correlates of primed vesicles. Interestingly, a subpopulation of membrane-contacting vesicles, located within 30 nm of a dense projection, are unperturbed in unc-13 mutants. We show that UNC-10/Rim, a protein implicated in presynaptic plasticity, localizes to dense projections and that loss of UNC-10/Rim causes an UNC-13-independent reduction in membrane-contacting synaptic vesicles within 30 nm of the dense projections. Our data together identify a discrete domain for vesicle priming within 100 nm of dense projections and further suggest that UNC-10/Rim and UNC-13 separately contribute to the membrane localization of synaptic vesicles within this domain.

Mesh Headings (Keywords): Animals, Caenorhabditis elegans, Caenorhabditis elegans Proteins, Carrier Proteins, Cells, Cultured, Membrane Microdomains, Nerve Tissue Proteins, Synaptic Vesicles


Check for Full Text / PubMed Unique Identifier (PMID): 16885217


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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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