RACK-1 acts with Rac GTPase signaling and UNC-115/abLIM in Caenorhabditis elegans axon pathfinding and cell migration

PLoS Genet. 2010 Nov 18;6(11):e1001215. doi: 10.1371/journal.pgen.1001215.

Abstract

Migrating cells and growth cones extend lamellipodial and filopodial protrusions that are required for outgrowth and guidance. The mechanisms of cytoskeletal regulation that underlie cell and growth cone migration are of much interest to developmental biologists. Previous studies have shown that the Arp2/3 complex and UNC-115/abLIM act redundantly to mediate growth cone lamellipodia and filopodia formation and axon pathfinding. While much is known about the regulation of Arp2/3, less is known about regulators of UNC-115/abLIM. Here we show that the Caenorhabditis elegans counterpart of the Receptor for Activated C Kinase (RACK-1) interacts physically with the actin-binding protein UNC-115/abLIM and that RACK-1 is required for axon pathfinding. Genetic interactions indicate that RACK-1 acts cell-autonomously in the UNC-115/abLIM pathway in axon pathfinding and lamellipodia and filopodia formation, downstream of the CED-10/Rac GTPase and in parallel to MIG-2/RhoG. Furthermore, we show that RACK-1 is involved in migration of the gonadal distal tip cells and that the signaling pathways involved in this process might be distinct from those involved in axon pathfinding. In sum, these studies pinpoint RACK-1 as a component of a novel signaling pathway involving Rac GTPases and UNC-115/abLIM and suggest that RACK-1 might be involved in the regulation of the actin cytoskeleton and lamellipodia and filopodia formation in migrating cells and growth cones.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Axons / metabolism*
  • Base Sequence
  • Caenorhabditis elegans / cytology*
  • Caenorhabditis elegans / enzymology
  • Caenorhabditis elegans Proteins / chemistry
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism*
  • Cell Movement*
  • Green Fluorescent Proteins / metabolism
  • Immunoprecipitation
  • Microfilament Proteins / chemistry
  • Microfilament Proteins / genetics
  • Microfilament Proteins / metabolism*
  • Models, Biological
  • Molecular Sequence Data
  • Motor Neurons / cytology
  • Motor Neurons / metabolism
  • Mutation / genetics
  • Organ Specificity
  • Protein Binding
  • Pseudopodia / metabolism
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Recombinant Fusion Proteins / metabolism
  • Signal Transduction*
  • Two-Hybrid System Techniques
  • rac GTP-Binding Proteins / metabolism*

Substances

  • CED-10 protein, C elegans
  • Caenorhabditis elegans Proteins
  • Microfilament Proteins
  • RACK-1 protein, C elegans
  • Receptors, Cytoplasmic and Nuclear
  • Recombinant Fusion Proteins
  • UNC-115 protein, C elegans
  • Green Fluorescent Proteins
  • rac GTP-Binding Proteins