Sensory regulated Wnt production from neurons helps make organ development robust to environmental changes in C. elegans

Development. 2020 Jul 23;147(14):dev186080. doi: 10.1242/dev.186080.

Abstract

Long-term survival of an animal species depends on development being robust to environmental variations and climate changes. We used C. elegans to study how mechanisms that sense environmental changes trigger adaptive responses that ensure animals develop properly. In water, the nervous system induces an adaptive response that reinforces vulval development through an unknown backup signal for vulval induction. This response involves the heterotrimeric G-protein EGL-30//Gαq acting in motor neurons. It also requires body-wall muscle, which is excited by EGL-30-stimulated synaptic transmission, suggesting a behavioral function of neurons induces backup signal production from muscle. We now report that increased acetylcholine during liquid growth activates an EGL-30-Rho pathway, distinct from the synaptic transmission pathway, that increases Wnt production from motor neurons. We also provide evidence that this neuronal Wnt contributes to EGL-30-stimulated vulval development, with muscle producing a parallel developmental signal. As diverse sensory modalities stimulate motor neurons via acetylcholine, this mechanism enables broad sensory perception to enhance Wnt-dependent development. Thus, sensory perception improves animal fitness by activating distinct neuronal functions that trigger adaptive changes in both behavior and developmental processes.

Keywords: Elegans; GNAQ; Neuron; Robustness; Vulval development; Wnt.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / metabolism
  • Actin Cytoskeleton
  • Animals
  • Animals, Genetically Modified / growth & development
  • Animals, Genetically Modified / metabolism
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / growth & development
  • Caenorhabditis elegans / metabolism*
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism*
  • Epidermal Growth Factor / metabolism
  • Female
  • GTP-Binding Protein alpha Subunits, Gq-G11 / genetics
  • GTP-Binding Protein alpha Subunits, Gq-G11 / metabolism
  • Genotype
  • Mutagenesis
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neurons / metabolism*
  • Signal Transduction
  • Synaptic Transmission / genetics
  • Vulva / growth & development
  • Vulva / metabolism
  • Wnt Proteins / genetics
  • Wnt Proteins / metabolism*

Substances

  • CWN-1 protein, C elegans
  • Caenorhabditis elegans Proteins
  • Egl-30 protein, C elegans
  • Nerve Tissue Proteins
  • UNC-73 protein, C elegans
  • Wnt Proteins
  • Lin-3 protein, C elegans
  • Epidermal Growth Factor
  • GTP-Binding Protein alpha Subunits, Gq-G11
  • Acetylcholine