Disease-Causing Mutations in the G Protein G alpha s Subvert the Roles of GDP and GTP

摘要

The single most frequent cancer-causing mutation across all heterotrimeric G proteins is R201C in G alpha s. The current model explaining the gain-of-function activity of the R201 mutations is through the loss of GTPase activity and resulting inability to switch off to the GDP state. Here, we find that the R201C mutation can bypass the need for GTP binding by directly activating GDP-bound G alpha s through stabilization of an intramolecular hydrogen bond network. Having found that a gain-of-function mutation can convert GDP into an activator, we postulated that a reciprocal mutation might disrupt the normal role of GTP. Indeed, we found R228C, a loss-of-function mutation in G alpha s that causes pseudohypoparathyroidism type 1a (PHP-Ia), compromised the adenylyl cyclase-activating activity of G alpha s bound to a non-hydrolyzable GTP analog. These findings show that disease-causing mutations in G alpha s can subvert the canonical roles of GDP and GTP, providing new insights into the regulation mechanism of G proteins.