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A LIM-homeodomain combinatorial code for motor-neuron pathway selection

Author

Listed:
  • Stefan Thor

    (Molecular Neurobiology Laboratory, The Salk Institute
    Harvard Medical School)

  • Siv G. E. Andersson

    (Center for Neurobiology and Behavior, College of Physicians and Surgeons of Columbia University)

  • Andrew Tomlinson

    (Center for Neurobiology and Behavior, College of Physicians and Surgeons of Columbia University)

  • John B. Thomas

    (Molecular Neurobiology Laboratory, The Salk Institute)

Abstract

Different classes of vertebrate motor neuron that innervate distinct muscle targets express unique combinations of LIM-homeodomain transcription factors1,2, suggesting that a combinatorial code of LIM-homeodomain proteins may underlie the control of motor-neuron pathway selection. Studies of LIM-homeodomain genes in mouse, Drosophila melanogaster and Caenorhabditis elegans have revealed functions of these genes in neuronal survival, axon guidance, neurotransmitter expression and neuronal function3,4,5,6,7,8, but, to our knowledge, none of these studies have addressed the issue of a functional code. Here we study two members of this gene family in Drosophila, namely lim3, the homologue of the vertebrate Lhx3 and Lhx4 genes, and islet, thehomologue of the vertebrate Isl1 and Isl2 genes. We show that Drosophila lim3 is expressed by a specific subset of islet-expressing motor neurons and that mutating or misexpressing lim3 switches motor-neuron projections predictably. Our results provide evidence that lim3 and islet constitute a combinatorial code that generates distinct motor-neuron identities.

Suggested Citation

  • Stefan Thor & Siv G. E. Andersson & Andrew Tomlinson & John B. Thomas, 1999. "A LIM-homeodomain combinatorial code for motor-neuron pathway selection," Nature, Nature, vol. 397(6714), pages 76-80, January.
    • Handle: RePEc:nat:nature:v:397:y:1999:i:6714:d:10.1038_16275
    DOI: 10.1038/16275
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