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Genetic Analysis of LET-23 Mediated IP₃ Signaling in Caenorhabditis elegans

Citation

Bui, Yêń Kim (2003) Genetic Analysis of LET-23 Mediated IP₃ Signaling in Caenorhabditis elegans. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/92D0-6V64. https://resolver.caltech.edu/CaltechETD:etd-09092002-222935

Abstract

Our understanding of signal transduction has increased from the use of genetically tractable organisms combined with biochemical anaylsis in cell culture. An example is LET-23 receptor tyrosine kinase signaling in Caenorhabditis elegans. The epidermal growth factor receptor homolog, LET-23 RTK, mediates multiple functions: development of the male tale, vulva induction, viability, and fertility. One of the ways in which activation of the same receptor can generate a specific response is through distinct signaling pathways downstream. Fertility is mediated by a RAS-independent inositol 1,4,5- triphopshate (IP₃) signaling pathway downstream of LET-23 activation.

In this thesis, I take a genetic route to the analysis of IP₃ signaling in C. elegans, which mediates ovulation in the fertility pathway. Genetic screens for suppressor or enhancers of mutant phenotypes remain an imporant tool for dissecting signaling pathways. They can uncover new genes or new mutations in existing genes, which upon analysis, will help us understand more about how that particular protein functions. I describe a genetic screen to identify genes that act to suppress the ovulation/sterility defects associated with both a a gain of function in the IP₃ receptor and loss of function in the IP₃ 3-kinase. Initial characterization of four suppressors identified are reported. Disruption of genes identified by genome sequencing has allowed us to determine whether a protein is essential for a given response. The importance of regulating IP₃ levels is ilustrated by the complexity of kinases and phosphatases that metabolize IP₃. Nomarksi video microscopy analysis shows the C. elegans IP₃ 3-kinase defective mutant, lfe-2, has no ovulation phenotype. Using reverse genetics, I targeted a deletion in the C. elegans 5-phosphatase, ipp-5, and demonstrate that IPP-5 plays a critical negative regulatory function for distal spermatheca contraction behavior. Evidence for levels of IP₃ signaling regulating spermatheca contractions, which affects fertitlity, comes from my analysis of multiple mutants that perturb IP₃ signaling. The work presented in this thesis provide the most extensive genetic analysis of IP₃ signaling to date. These results imply thresholds are important for achieving an appropriate response. Finally, I present the genetic characterization of a novel phospholipase C, Ce PLC210 and implicate its critical function for regulating spermatheca-uturine valve contraction behavior. A multitude of proteins is involved in generating a precise biological response.

Item Type:Thesis (Dissertation (Ph.D.))
Subject Keywords:5-phosphatase; C. elegans; inositol triphosphate; ovulation; phospholipase C; rhythmic behavior
Degree Grantor:California Institute of Technology
Division:Biology
Major Option:Biology
Thesis Availability:Public (worldwide access)
Research Advisor(s):
  • Sternberg, Paul W.
Thesis Committee:
  • Sternberg, Paul W. (chair)
  • Meyerowitz, Elliot M.
  • Schuman, Erin Margaret
  • Deshaies, Raymond Joseph
  • Fraser, Scott E.
Defense Date:20 June 2002
Record Number:CaltechETD:etd-09092002-222935
Persistent URL:https://resolver.caltech.edu/CaltechETD:etd-09092002-222935
DOI:10.7907/92D0-6V64
Default Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:3396
Collection:CaltechTHESIS
Deposited By: Imported from ETD-db
Deposited On:16 Sep 2002
Last Modified:01 Sep 2022 23:54

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