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

  1. Gidi Shemer and
  2. Benjamin Podbilewicz1
  1. Department of Biology, Technion-Israel Institute of Technology, Haifa, 32000, Israel

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 inCaenorhabditis 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.

Keywords

Footnotes

  • 1 Corresponding author.

  • E-MAIL podbilew{at}tx.technion.ac.il; FAX 972-4-822-5153.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.251202.

    • Received October 4, 2002.
    • Accepted October 15, 2002.
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