Syntaxin-1 N-peptide and Habc-domain perform distinct essential functions in synaptic vesicle fusion

EMBO J. 2013 Jan 9;32(1):159-71. doi: 10.1038/emboj.2012.307. Epub 2012 Nov 27.

Abstract

Among SNARE proteins mediating synaptic vesicle fusion, syntaxin-1 uniquely includes an N-terminal peptide ('N-peptide') that binds to Munc18-1, and a large, conserved H(abc)-domain that also binds to Munc18-1. Previous in vitro studies suggested that the syntaxin-1 N-peptide is functionally important, whereas the syntaxin-1 H(abc)-domain is not, but limited information is available about the in vivo functions of these syntaxin-1 domains. Using rescue experiments in cultured syntaxin-deficient neurons, we now show that the N-peptide and the H(abc)-domain of syntaxin-1 perform distinct and independent roles in synaptic vesicle fusion. Specifically, we found that the N-peptide is essential for vesicle fusion as such, whereas the H(abc)-domain regulates this fusion, in part by forming the closed syntaxin-1 conformation. Moreover, we observed that deletion of the H(abc)-domain but not deletion of the N-peptide caused a loss of Munc18-1 which results in a decrease in the readily releasable pool of vesicles at a synapse, suggesting that Munc18 binding to the H(abc)-domain stabilizes Munc18-1. Thus, the N-terminal syntaxin-1 domains mediate different functions in synaptic vesicle fusion, probably via formation of distinct Munc18/SNARE-protein complexes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Animals, Newborn
  • Cells, Cultured
  • Gene Knockdown Techniques
  • Membrane Fusion
  • Mice
  • Molecular Sequence Data
  • Munc18 Proteins / metabolism*
  • Neurons / metabolism*
  • Peptides / chemistry
  • Peptides / genetics
  • Peptides / metabolism*
  • Protein Binding
  • Protein Conformation
  • Protein Interaction Mapping
  • Protein Structure, Tertiary
  • Synapses / genetics
  • Synapses / metabolism*
  • Synaptic Transmission
  • Synaptic Vesicles / genetics
  • Synaptic Vesicles / metabolism
  • Syntaxin 1 / chemistry
  • Syntaxin 1 / genetics
  • Syntaxin 1 / metabolism*

Substances

  • Munc18 Proteins
  • Peptides
  • Stxbp1 protein, mouse
  • Syntaxin 1