Synaptojanin is recruited by endophilin to promote synaptic vesicle uncoating

Neuron. 2003 Nov 13;40(4):733-48. doi: 10.1016/s0896-6273(03)00644-5.

Abstract

We describe the isolation and characterization of Drosophila synaptojanin (synj) mutants. synj encodes a phosphatidylinositol phosphatase involved in clathrin-mediated endocytosis. We show that Synj is specifically localized to presynaptic terminals and is associated with synaptic vesicles. The electrophysiological and ultrastructural defects observed in synj mutants are strikingly similar to those found in endophilin mutants, and Synj and Endo colocalize and interact biochemically. Moreover, synj; endo double mutant synaptic terminals exhibit properties that are very similar to terminals of each single mutant, and overexpression of Endophilin can partially rescue the functional defects in partial loss-of-function synj mutants. Interestingly, Synj is mislocalized and destabilized at synapses devoid of Endophilin, suggesting that Endophilin recruits and stabilizes Synj on newly formed vesicles to promote vesicle uncoating. Our data also provide further evidence that kiss-and-run is able to maintain neurotransmitter release when synapses are not extensively challenged.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Comment

MeSH terms

  • Adaptor Proteins, Signal Transducing*
  • Animals
  • Animals, Genetically Modified
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cell Differentiation / genetics
  • Clathrin / metabolism
  • Down-Regulation / genetics
  • Drosophila melanogaster
  • Endocytosis / genetics
  • Female
  • Gene Expression Regulation, Developmental / genetics
  • Male
  • Membrane Fusion / genetics
  • Microscopy, Electron
  • Mutation / genetics
  • Nerve Tissue Proteins / deficiency
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Phenotype
  • Phosphoric Monoester Hydrolases / deficiency
  • Phosphoric Monoester Hydrolases / genetics
  • Phosphoric Monoester Hydrolases / metabolism*
  • Photoreceptor Cells, Invertebrate / metabolism
  • Photoreceptor Cells, Invertebrate / pathology
  • Photoreceptor Cells, Invertebrate / ultrastructure
  • Presynaptic Terminals / metabolism*
  • Presynaptic Terminals / pathology
  • Presynaptic Terminals / ultrastructure
  • Synaptic Transmission / genetics*
  • Synaptic Vesicles / metabolism*
  • Synaptic Vesicles / pathology
  • Synaptic Vesicles / ultrastructure

Substances

  • Adaptor Proteins, Signal Transducing
  • Carrier Proteins
  • Clathrin
  • Nerve Tissue Proteins
  • synaptojanin
  • Phosphoric Monoester Hydrolases