Hippo-independent activation of YAP by the GNAQ uveal melanoma oncogene through a Trio-regulated Rho GTPase Signaling Circuitry

Abstract

Mutually exclusive activating mutations in the GNAQ and GNA11 oncogenes, encoding heterotrimeric Gαq family members, have been identified in ~83% and ~6% of uveal and skin melanomas, respectively. However, the molecular events underlying these GNAQ-driven malignancies are not yet defined, thus limiting the ability to develop cancer-targeted therapies. Here, we focused on the transcriptional coactivator YAP, a critical component of the Hippo signaling pathway that controls organ size. We found that Gαq stimulates YAP through a Trio-Rho/Rac signaling circuitry promoting actin polymerization, independently of phospholipase Cβ and the canonical Hippo pathway. Furthermore, we show that Gαq promotes the YAP-dependent growth of uveal melanoma cells, thereby identifying YAP as a suitable therapeutic target in uveal melanoma, a GNAQ/. GNA11-initiated human malignancy. •The GNAQ oncogene stimulates the transcriptional coactivator YAP in uveal melanoma•A Hippo- and PLCβ-independent Rho GTPase signaling circuitry links GNAQ to YAP•YAP is essential for GNAQ-induced uveal melanoma cell proliferation•YAP represents a suitable therapeutic target for melanomas harboring GNAQ mutations. Feng etal. find that aberrant Gαq/11 activation due to oncogenic mutations leads to YAP-dependent growth in uveal melanoma. In this context, YAP stimulation is independent of PLCβ and the canonical Hippo pathway and instead acts through Trio-Rho/Rac signaling and actin polymerization. © 2014 Elsevier Inc.