Crosstalk between the EGFR and LIN-12/Notch pathways in C. elegans vulval development

Science. 2004 Jan 30;303(5658):663-6. doi: 10.1126/science.1091639.

Abstract

The Caenorhabditis elegans vulva is an important paradigm for cell-cell interactions in animal development. The fates of six vulval precursor cells are patterned through the action of the epidermal growth factor receptor-mitogen-activated protein kinase (EGFR-MAPK) inductive signaling pathway, which specifies the 1 degrees fate, and the LIN-12/Notch lateral signaling pathway, which specifies the 2 degrees fate. Here, we provide evidence that the inductive signal is spatially graded and initially activates the EGFR-MAPK pathway in the prospective 2 degrees cells. Subsequently, this effect is counteracted by the expression of multiple new negative regulators of the EGFR-MAPK pathway, under direct transcriptional control of the LIN-12-mediated lateral signal.

Publication types

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

MeSH terms

  • Animals
  • Caenorhabditis elegans / cytology
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / growth & development*
  • Caenorhabditis elegans / metabolism
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism*
  • Cell Cycle Proteins / metabolism
  • ErbB Receptors / metabolism*
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental
  • Genes, Helminth
  • Genes, Reporter
  • Green Fluorescent Proteins
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Lac Operon
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • MAP Kinase Signaling System
  • Membrane Proteins / metabolism*
  • Mitogen-Activated Protein Kinases / metabolism
  • Models, Biological
  • Morphogenesis
  • Protein Tyrosine Phosphatases / metabolism
  • Receptors, Notch
  • Recombinant Fusion Proteins
  • Signal Transduction*
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Transcription, Genetic
  • Vulva / cytology
  • Vulva / growth & development
  • Vulva / metabolism

Substances

  • Caenorhabditis elegans Proteins
  • Cell Cycle Proteins
  • Egl-17 protein, C elegans
  • Intercellular Signaling Peptides and Proteins
  • Lin-12 protein, C elegans
  • Luminescent Proteins
  • Membrane Proteins
  • Receptors, Notch
  • Recombinant Fusion Proteins
  • Green Fluorescent Proteins
  • ErbB Receptors
  • let-23 protein, C elegans
  • Mitogen-Activated Protein Kinases
  • lip-1 protein, C elegans
  • Protein Tyrosine Phosphatases