Direct regulation of p190RhoGEF by activated Rho and Rac GTPases

作者：Dada Olugbenga; Gutowski Stephen; Brautigam Chad A; Chen Zhe; Sternweis Paul C^*

来源：Journal of Structural Biology, 2018, 202(1): 13-24.

DOI：10.1016/j.jsb.2017.11.014

• RhoGEF
• PH domain
• GTPase
• Crosstalk
• Crystal structure
• Membrane localization

Rho family GTPases regulate a wide range of cellular processes. This includes cellular dynamics where three subfamilies, Rho, Rac, and Cdc42, are known to regulate cell shape and migration though coordinate action. Activation of Rho proteins largely depends on Rho Guanine nucleotide Exchange Factors (RhoGEFs) through a catalytic Dbl homology (DH) domain linked to a pleckstrin homology (PH) domain that subserves various functions. The PH domains from Lbc RhoGEFs, which specifically activate RhoA, have been shown to bind to activated RhoA. Here, p190RhoGEF is shown to also bind Racl.GTP. Crystal structures reveal that activated Racl and RhoA use their effector-binding surfaces to associate with the same hydrophobic surface on the PH domain. Both activated RhoA and Racl can stimulate exchange of nucleotide on RhoA by localization of p190RhoGEF to its substrate, RhoA.GDP, in vitro. The binding of activated RhoA provides a mechanism for positive feedback regulation as previously proposed for the family of Lbc RhoGEFs. In contrast, the novel interaction between activated Racl and p190RhoGEF reveals a potential mechanism for cross-talk regulation where Rac can directly effect stimulation of RhoA. The greater capacity of Racl to stimulate p190RhoGEF among the Lbc RhoGEFs suggests functional specialization.

• 出版日期2018-4