LIN-39/Hox triggers cell division and represses EFF-1/fusogen-dependent vulval cell fusion

Genes Dev. 2002 Dec 15;16(24):3136-41. doi: 10.1101/gad.251202.

Abstract

General mechanisms by which Hox genes establish cell fates are known. However, a few Hox effectors mediating cell behaviors have been identified. Here we found the first effector of LIN-39/HoxD4/Dfd in Caenorhabditis elegans. In specific vulval precursor cells (VPCs), LIN-39 represses early and late expression of EFF-1, a membrane protein essential for cell fusion. Repression of eff-1 is also achieved by the activity of CEH-20/Exd/Pbx, a known cofactor of Hox proteins. Unfused VPCs in lin-39(-);eff-1(-) double mutants fail to divide but migrate, executing vulval fates. Thus, lin-39 is essential for inhibition of EFF-1-dependent cell fusion and stimulation of cell proliferation during vulva formation. Supplemental material is available at http://www.genesdev.org.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Binding Sites
  • Caenorhabditis elegans / cytology*
  • Caenorhabditis elegans Proteins / physiology*
  • Cell Differentiation
  • Cell Division
  • Cell Fusion
  • Embryonic Induction
  • Female
  • Fluorescent Antibody Technique
  • Gene Expression Regulation, Developmental
  • Helminth Proteins / metabolism
  • Homeodomain Proteins / physiology*
  • Homozygote
  • Membrane Proteins / physiology*
  • Models, Molecular
  • Mutation
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Stem Cells / metabolism
  • Transcription Factors*
  • Vulva / cytology*

Substances

  • Caenorhabditis elegans Proteins
  • Helminth Proteins
  • Homeodomain Proteins
  • Membrane Proteins
  • Recombinant Proteins
  • Transcription Factors
  • ceh-20 protein, C elegans
  • lin-39 protein, C elegans