UNC-6 and UNC-40 promote dendritic growth through PAR-4 in Caenorhabditis elegans neurons

Nat Neurosci. 2011 Feb;14(2):165-72. doi: 10.1038/nn.2717. Epub 2010 Dec 26.

Abstract

Axons navigating through the developing nervous system are instructed by external attractive and repulsive cues. Emerging evidence suggests the same cues control dendrite development, but it is not understood how they differentially instruct axons and dendrites. We studied a C. elegans motor neuron whose axon and dendrite adopt different trajectories and lengths. We found that the guidance cue UNC-6 (Netrin) is required for both axon and dendrite development. Its repulsive receptor UNC-5 repelled the axon from the ventral cell body, whereas the attractive receptor UNC-40 (DCC) was dendritically enriched and promotes antero-posterior dendritic growth. Although the endogenous ventrally secreted UNC-6 instructs axon guidance, dorsal or even membrane-tethered UNC-6 could support dendrite development. Unexpectedly, the serine-threonine kinase PAR-4 (LKB1) was selectively required for the activity of the UNC-40 pathway in dendrite outgrowth. These data suggest that axon and dendrite of one neuron interpret common environmental cues with different receptors and downstream signaling pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Caenorhabditis elegans
  • Caenorhabditis elegans Proteins / metabolism*
  • Cell Adhesion Molecules / metabolism*
  • Cell Movement / physiology
  • Dendrites / physiology*
  • Nerve Tissue Proteins / metabolism*
  • Netrins
  • Neurons / physiology*
  • Protein Serine-Threonine Kinases
  • Receptors, Cell Surface / metabolism
  • Signal Transduction / physiology

Substances

  • Caenorhabditis elegans Proteins
  • Cell Adhesion Molecules
  • Nerve Tissue Proteins
  • Netrins
  • Receptors, Cell Surface
  • UNC-40 protein, C elegans
  • UNC-6 protein, C elegans
  • UNC-5 protein, C elegans
  • PAR-3 protein, C elegans
  • Protein Serine-Threonine Kinases