Interaction of Protein Kinase C Isozymes with Rho GTPases

Publisher Website
Google Scholar
Abstract
Evidence is provided for direct protein−protein interactions between protein kinase C (PKC) α, βI, βII, γ, δ, ε, and ζ and members of the Rho family of small GTPases. Previous investigations, based on the immunoprecipitation approach, have provided evidence consistent with a direct interaction, but this remained to be proven. In the study presented here, an in vitro assay, consisting only of purified proteins and the requisite PKC activators and cofactors, was used to determine the effects of Rho GTPases on the activities of the different PKC isoforms. It was found that the activity of PKCα was potently enhanced by RhoA and Cdc42 and to a lesser extent by Rac1, whereas the effects on the activities of PKCβI, -βII, -γ, -δ, -ε, and -ζ were much reduced. These results indicate a direct interaction between PKCα and each of the Rho GTPases. However, the Rho GTPase concentration dependencies for the potentiating effects on PKCα activity differed for each Rho GTPase and were in the following order: RhoA > Cdc42 > Rac1. PKCα was activated in a phorbol ester- and Ca2+-dependent manner. This was reflected by a substantial decrease in the phorbol ester concentration requirements for activity in the presence of Ca2+, which for each Rho GTPase was induced within a low nanomolar phorbol ester concentration range. The activity of PKCα also was found to be dependent on the nature of the GTP- or GDP-bound state of the Rho GTPases, suggesting that the interaction may be regulated by conformational changes in both PKCα and Rho GTPases. Such an interaction could result in significant cross-talk between the distinct pathways regulated by these two signaling elements.