Dynactin is necessary for synapse stabilization

Neuron. 2002 May 30;34(5):729-41. doi: 10.1016/s0896-6273(02)00721-3.

Abstract

We present evidence that synapse retraction occurs during normal synaptic growth at the Drosophila neuromuscular junction (NMJ). An RNAi-based screen to identify the molecular mechanisms that regulate synapse retraction identified Arp-1/centractin, a subunit of the dynactin complex. Arp-1 dsRNA enhances synapse retraction, and this effect is phenocopied by a mutation in P150/Glued, also a dynactin component. The Glued protein is enriched within the presynaptic nerve terminal, and presynaptic expression of a dominant-negative Glued transgene enhances retraction. Retraction is associated with a local disruption of the synaptic microtubule cytoskeleton. Electrophysiological, ultrastructural, and immunohistochemical data support a model in which presynaptic retraction precedes disassembly of the postsynaptic apparatus. Our data suggests that dynactin functions locally within the presynaptic arbor to promote synapse stability.

Publication types

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

MeSH terms

  • Actins / genetics
  • Actins / metabolism
  • Animals
  • Animals, Genetically Modified
  • Cell Differentiation / genetics
  • Central Nervous System / growth & development*
  • Central Nervous System / metabolism
  • Central Nervous System / ultrastructure
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism
  • Drosophila / growth & development*
  • Drosophila / metabolism
  • Drosophila / ultrastructure
  • Drosophila Proteins
  • Dynactin Complex
  • Female
  • Gene Expression Regulation, Developmental / genetics
  • Male
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism*
  • Motor Neurons / metabolism*
  • Motor Neurons / ultrastructure
  • Mutation / genetics
  • Neuromuscular Junction / growth & development*
  • Neuromuscular Junction / metabolism
  • Neuromuscular Junction / ultrastructure
  • Neuronal Plasticity / genetics
  • Presynaptic Terminals / metabolism*
  • Presynaptic Terminals / pathology
  • Presynaptic Terminals / ultrastructure
  • RNA / genetics
  • Transgenes / genetics

Substances

  • ACTRT3 protein, human
  • Actins
  • Cytoskeletal Proteins
  • DCTN1 protein, human
  • DCTN1-p150 protein, Drosophila
  • Drosophila Proteins
  • Dynactin Complex
  • Microtubule-Associated Proteins
  • RNA