A Genome-Wide Rnai Screen Reveals A Trio-Regulated Rho Gtpase Circuitry Transducing Mitogenic Signals Initiated By G Protein-Coupled Receptors

Activating mutations in GNAQ and GNA11, encoding members of the G alpha(q) family of G protein alpha subunits, are the driver oncogenes in uveal melanoma, and mutations in Gq-linked G protein-coupled receptors have been identified recently in numerous human malignancies. How G alpha(q) and its coupled receptors transduce mitogenic signals is still unclear because of the complexity of signaling events perturbed upon Gq activation. Using a synthetic-biology approach and a genome-wide RNAi screen, we found that a highly conserved guanine nucleotide exchange factor, Trio, is essential for activating Rhoand Rac-regulated signaling pathways acting on JNK and p38, and thereby transducing proliferative signals from G alpha(q) to the nucleus independently of phospholipase C-beta. Indeed, whereas many biological responses elicited by Gq depend on the transient activation of second-messenger systems, Gq utilizes a hard-wired protein-protein-interaction-based signaling circuitry to achieve the sustained stimulation of proliferative pathways, thereby controlling normal and aberrant cell growth.