A Forward Genetic Screen for Molecules Involved in Pheromone-Induced Dauer Formation in Caenorhabditis elegans

G3 (Bethesda). 2016 May 3;6(5):1475-87. doi: 10.1534/g3.115.026450.

Abstract

Animals must constantly assess their surroundings and integrate sensory cues to make appropriate behavioral and developmental decisions. Pheromones produced by conspecific individuals provide critical information regarding environmental conditions. Ascaroside pheromone concentration and composition are instructive in the decision of Caenorhabditis elegans to either develop into a reproductive adult or enter into the stress-resistant alternate dauer developmental stage. Pheromones are sensed by a small set of sensory neurons, and integrated with additional environmental cues, to regulate neuroendocrine signaling and dauer formation. To identify molecules required for pheromone-induced dauer formation, we performed an unbiased forward genetic screen and identified phd (pheromone response-defective dauer) mutants. Here, we describe new roles in dauer formation for previously identified neuronal molecules such as the WD40 domain protein QUI-1 and MACO-1 Macoilin, report new roles for nociceptive neurons in modulating pheromone-induced dauer formation, and identify tau tubulin kinases as new genes involved in dauer formation. Thus, phd mutants define loci required for the detection, transmission, or integration of pheromone signals in the regulation of dauer formation.

Keywords: C. elegans; che-12; dauer; maco-1; pheromone; qui-1; ttbk.

Publication types

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

MeSH terms

  • Animals
  • Caenorhabditis elegans / drug effects*
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans / growth & development
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism
  • Chromosome Mapping
  • Genetic Association Studies*
  • Genetic Complementation Test
  • Genetic Linkage
  • Genetic Testing*
  • Genome, Helminth
  • Genomics / methods
  • High-Throughput Nucleotide Sequencing
  • Mutation
  • Pheromones / pharmacology*
  • Signal Transduction / drug effects
  • Stress, Physiological / drug effects*
  • Stress, Physiological / genetics*

Substances

  • Caenorhabditis elegans Proteins
  • Pheromones