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Prenylated protein regulation in the Caenorhabditis elegans brain

Objective

"Protein prenylation is essential for the viability of all eukaryotic cells. Prenylated proteins regulate fundamental processes such as cell growth, differentiation and movement. Therefore, it is not surprising that prenylated proteins play a critical role in the pathophysiology of human diseases such as cancer and atherosclerosis. Indeed, mutations in the farnesylated oncogene Ras are found in 10-15% of all human tumors. Recent studies demonstrated that PDE6D acts as a soluble chaperon of Ras, thus it might regulate its oncogenic activity. In addition, PDE6D is important for the efficient transport of the rhodopsin kinase GRK1 and the alpha and beta subunits of PDE6 from the ER to the outer segments of cones and rods cells. Thus may play a critical role in normal vision physiology. PDE6D is conserved and has homologs across the animal kingdom. In the C. elegans worm, RNAi experiments against the PDE6D homolog pdl-1 failed to produce any abnormalities in the nematode physiology or behavior. However, we isolated a pdl-1 suppressor mutant that inhibits the fast recovery of worms after hypoxic stress.
We demonstrated that pdl-1 regulate the correct localization of the O2 sensor gcy-35. Thus, pdl-1 is essential for normal O2 responses in the C. elegans worm. Based on those finding my research proposal aims to:
1) Understand how pdl-1 is transported inside cells and elucidate novel regulators of its activity.
2) Identify new PDL-1 substrates, and explore their function in the C. elegans brain.
Hence, my research proposal aim is to understand protein prenylation regulation at all levels; from the molecular signaling network to the physiology and behavior of the whole animal. For this aim, we use behavioral paradigms together with state of the art microscopy, biochemistry and computational methods. We hope that our studies will strengthen the prenylated protein field in Europe and assist in development of better therapies for cancer, and atherosclerosis diseases."

Call for proposal

FP7-PEOPLE-2012-CIG
See other projects for this call

Funding Scheme

MC-CIG - Support for training and career development of researcher (CIG)

Coordinator

THE HEBREW UNIVERSITY OF JERUSALEM
Address
Edmond J Safra Campus Givat Ram
91904 Jerusalem
Israel
Activity type
Higher or Secondary Education Establishments
EU contribution
€ 100 000
Administrative Contact
Hani Ben Yehuda (Ms.)