The UNC-6/Netrin receptors UNC-40/DCC and UNC-5 inhibit growth cone filopodial protrusion via UNC-73/Trio, Rac-like GTPases and UNC-33/CRMP

Development. 2014 Nov;141(22):4395-405. doi: 10.1242/dev.110437.

Abstract

UNC-6/Netrin is a conserved axon guidance cue that can mediate both attraction and repulsion. We previously discovered that attractive UNC-40/DCC receptor signaling stimulates growth cone filopodial protrusion and that repulsive UNC-40-UNC-5 heterodimers inhibit filopodial protrusion in C. elegans. Here, we identify cytoplasmic signaling molecules required for UNC-6-mediated inhibition of filopodial protrusion involved in axon repulsion. We show that the Rac-like GTPases CED-10 and MIG-2, the Rac GTP exchange factor UNC-73/Trio, UNC-44/Ankyrin and UNC-33/CRMP act in inhibitory UNC-6 signaling. These molecules were required for the normal limitation of filopodial protrusion in developing growth cones and for inhibition of growth cone filopodial protrusion caused by activated MYR::UNC-40 and MYR::UNC-5 receptor signaling. Epistasis studies using activated CED-10 and MIG-2 indicated that UNC-44 and UNC-33 act downstream of the Rac-like GTPases in filopodial inhibition. UNC-73, UNC-33 and UNC-44 did not affect the accumulation of full-length UNC-5::GFP and UNC-40::GFP in growth cones, consistent with a model in which UNC-73, UNC-33 and UNC-44 influence cytoskeletal function during growth cone filopodial inhibition.

Keywords: Axon repulsion; Caenorhabditis elegans; Filopodia; Growth cone; UNC-40/DCC; UNC-5; UNC-6.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Caenorhabditis elegans / embryology*
  • Caenorhabditis elegans Proteins / metabolism*
  • Cell Adhesion Molecules / metabolism*
  • Epistasis, Genetic / physiology
  • Growth Cones / physiology*
  • Nerve Growth Factors / metabolism
  • Nerve Tissue Proteins / metabolism*
  • Netrins
  • Pseudopodia / physiology*
  • Receptors, Cell Surface / metabolism*
  • Signal Transduction / genetics
  • Signal Transduction / physiology*
  • Time-Lapse Imaging
  • rac GTP-Binding Proteins / metabolism

Substances

  • Caenorhabditis elegans Proteins
  • Cell Adhesion Molecules
  • Nerve Growth Factors
  • Nerve Tissue Proteins
  • Netrins
  • Receptors, Cell Surface
  • UNC-40 protein, C elegans
  • UNC-6 protein, C elegans
  • UNC-73 protein, C elegans
  • unc-33 protein, C elegans
  • UNC-5 protein, C elegans
  • Mig-2 protein, C elegans
  • rac GTP-Binding Proteins