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
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Animals, Genetically Modified
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Binding Sites
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Caenorhabditis elegans / cytology*
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Caenorhabditis elegans Proteins / physiology*
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Cell Differentiation
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Cell Division
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Cell Fusion
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Embryonic Induction
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Female
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Fluorescent Antibody Technique
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Gene Expression Regulation, Developmental
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Helminth Proteins / metabolism
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Homeodomain Proteins / physiology*
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Homozygote
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Membrane Proteins / physiology*
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Models, Molecular
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Mutation
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Recombinant Proteins / genetics
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Recombinant Proteins / metabolism
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Stem Cells / metabolism
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Transcription Factors*
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Vulva / cytology*
Substances
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Caenorhabditis elegans Proteins
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Helminth Proteins
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Homeodomain Proteins
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Membrane Proteins
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Recombinant Proteins
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Transcription Factors
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ceh-20 protein, C elegans
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lin-39 protein, C elegans