UNC-4/UNC-37-dependent repression of motor neuron-specific genes controls synaptic choice in Caenorhabditis elegans

  1. Angela R. Winnier,
  2. James Y.-J. Meir,
  3. Jennifer M. Ross,
  4. Nektarios Tavernarakis,
  5. Monica Driscoll,
  6. Takeshi Ishihara,
  7. Isao Katsura, and
  8. David M. Miller III
  1. Department of Cell Biology, Vanderbilt University Medical Center, Nashville, Tennessee 37232 USA; Department of Molecular Biology and Biochemistry, Rutgers University, New Brunswick, New Jersey 08855 USA; National Institute of Genetics, Mishima, Japan

Abstract

The UNC-4 homeoprotein and the Groucho-like corepressor UNC-37 specify synaptic choice in the Caenorhabditis elegans motor neuron circuit. In unc-4 mutants, VA motor neurons are miswired with inputs from interneurons normally reserved for their lineal sisters, the VB motor neurons. Here we show that UNC-4 and UNC-37 function together in VA motor neurons to repress VB-specific genes and that this activity depends on physical contact between UNC-37 and a conserved Engrailed-like repressor domain (eh1) in UNC-4. Missense mutations in the UNC-4 eh1 domain disrupt interactions between UNC-4 and UNC-37 and result in the loss of UNC-4-dependent repressor activity in vivo. A compensatory amino acid substitution in UNC-37 suppresses specific unc-4 alleles by restoring physical interactions with UNC-4 as well as UNC-4-dependent repression of VB-specific genes. We propose that repression of VB-specific genes by UNC-4 and UNC-37 is necessary for the creation of wild-type inputs to VA motor neurons. The existence of mammalian homologs of UNC-4 and UNC-37 indicates that a similar mechanism could regulate synaptic choice in the vertebrate spinal cord.

Keywords

Footnotes

  • These authors contributed equally to this work.

  • Corresponding author.

  • E-MAIL david.miller{at}mcmail.vanderbilt.edu; FAX (615) 343-4539.

    • Received August 3, 1999.
    • Accepted September 14, 1999.
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