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Gαs directly drives PDZ-RhoGEF signaling to Cdc42
Journal of Biological ChemistryVol. 295Issue 50p16920–16928Published online: October 6, 2020- Alejandro Castillo-Kauil
- Irving García-Jiménez
- Rodolfo Daniel Cervantes-Villagrana
- Sendi Rafael Adame-García
- Yarely Mabell Beltrán-Navarro
- J. Silvio Gutkind
- and others
Cited in Scopus: 8Gα proteins promote dynamic adjustments of cell shape directed by actin-cytoskeleton reorganization via their respective RhoGEF effectors. For example, Gα13 binding to the RGS-homology (RH) domains of several RH-RhoGEFs allosterically activates these proteins, causing them to expose their catalytic Dbl-homology (DH)/pleckstrin-homology (PH) regions, which triggers downstream signals. However, whether additional Gα proteins might directly regulate the RH-RhoGEFs was not known. To explore this question, we first examined the morphological effects of expressing shortened RH-RhoGEF DH/PH constructs of p115RhoGEF/ARHGEF1, PDZ-RhoGEF (PRG)/ARHGEF11, and LARG/ARHGEF12.