4.4 Article

Mechanisms of Ephrin Receptor Protein Kinase-Independent Signaling in Amphid Axon Guidance in Caenorhabditis elegans

Journal

GENETICS
Volume 195, Issue 3, Pages 899-+

Publisher

GENETICS SOCIETY AMERICA
DOI: 10.1534/genetics.113.154393

Keywords

Ephrin; amphid; left-right asymmetry; Abl tyrosine kinase; phosphatidylinositol 3-kinase

Funding

  1. National Institutes of Health (NIH) Office of Research Infrastructure Programs [P40 OD010440]
  2. University of California, San Diego (UCSD)/Salk Training Grant in Developmental Biology of Neural Diseases [T32 HD007495]
  3. UCSD Neural Circuits Postdoctoral Training Program [T32 NS007220]
  4. Ruth S. Kirschstein National Research Service Award [F32 GM090652]
  5. US Public Health Service [NIH R01 GM054657]

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Eph receptors and their ephrin ligands are key conserved regulators of axon guidance and can function in a variety of signaling modes. Here we analyze the genetic and cellular requirements for Eph signaling in a Caenorhabditis elegans axon guidance choice point, the ventral guidance of axons in the amphid commissure. The C. elegans Eph receptor EFN-1 has both kinase-dependent and kinase-independent roles in amphid ventral guidance. Of the four C. elegans ephrins, we find that only EFN-1 has a major role in amphid axon ventral guidance, and signals in both a receptor kinase-dependent and kinase-independent manner. Analysis of EFN-1 and EFN-1 expression and tissue-specific requirements is consistent with a model in which VAB-1 acts in amphid neurons, interacting with EFN-1 expressed on surrounding cells. Unexpectedly, left-hand neurons are more strongly affected than right-hand neurons by loss of Eph signaling, indicating a previously undetected left-right asymmetry in the requirement for Eph signaling. By screening candidate genes involved in Eph signaling, we find that the Eph kinase-independent pathway involves the ABL-1 nonreceptor tyrosine kinase and possibly the phosphatidylinositol 3-kinase pathway. Overexpression of ABL-1 is sufficient to rescue EFN-1 ventral guidance defects cell autonomously. Our results reveal new aspects of Eph signaling in a single axon guidance decision in vivo.

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