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Title page for ETD etd-11282008-174034

Type of Document Dissertation
Author Cheng, Hua
URN etd-11282008-174034
Title Analysis of Eph receptor signaling during oocyte meiotic maturation in Caenorhabditis elegans
Degree PhD
Department cell and developmental biology
Advisory Committee
Advisor Name Title
David Miller Committee Chair
Chang Chung Committee Member
david greenstein Committee Member
Ethan Lee Committee Member
Jin Chen Committee Member
  • receptor trafficking
  • meiotic maturation
  • Caenorhabditis elegans -- Reproduction -- Regulation
  • Protein-tyrosine kinase -- Receptors
  • Eph receptor
  • G proteins -- Physiological effect
Date of Defense 2008-10-15
Availability unrestricted
A conserved biological feature of sexual reproduction in animals is that oocytes arrest in meiotic prophase and resume meiosis in response to extra-ovarian signals. In Caenorhabditis. elegans, a sperm-sensing mechanism regulates oocyte meiotic maturation and ovulation. Sperm release the major sperm protein (MSP) signal to promotes meiotic maturation by antagonizing Eph receptor signaling and counteracting inhibitory inputs from the gonadal sheath cells. I show that MSP promotes oocyte meiotic maturation in part through direct interaction with the VAB-1/Eph receptor. Four conserved proteins, including a disabled protein (DAB-1), a vav family GEF (VAV-1), a protein kinase C (PKC-1), and a STAM homolog (PQN-19), function with VAB-1 in oocytes. We also show that antagonistic Gáo/i and Gás signaling pathways function in the soma to regulate meiotic maturation in parallel to the VAB-1 pathway. Furthermore, I show that in the absence of MSP VAB-1 inhibits meiotic maturation while either in or in transit to the endocytic recycling compartment (ERC). VAB-1::GFP localization to the RAB-11-positive ERC is antagonized by MSP signaling. Two negative regulators of oocyte meiotic maturation, DAB-1/Disabled and RAN-1, interact with the VAB-1 receptor and are required for its accumulation in the ERC in the absence of MSP/sperm. Inactivation of the endosomal recycling regulators rme-1 or rab-11.1 causes a vab-1-dependent reduction in the meiotic maturation rate in the presence of MSP/sperm. In addition, I show that Gás signaling in the gonadal sheath cells, affects VAB-1::GFP trafficking in oocytes. Taken together, our findings show that oocyte Eph receptor and somatic cell G protein signaling pathways control meiotic diapause in C. elegans, highlighting contrasts and parallels between MSP signaling in C. elegans and luteinizing hormone signaling in mammals. Moreover, my finding suggests that regulated endocytic trafficking of the VAB-1/Eph receptor contributes to the control of oocyte meiotic maturation in C. elegans. Eph receptor trafficking in other systems may be influenced by the conserved proteins DAB-1/Disabled and RAN-1 and by cross-talk with G-protein signaling in neighboring cells.

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