Binding of the cytosolic p200 protein to Golgi membranes is regulated by heterotrimeric G proteins

Abstract

The formation of vesicles for protein trafficking requires the dynamic binding of cytosolic coat proteins onto Golgi membranes and this binding is regulated by a variety of GTPases, including heterotrimeric G pro-teins. We have previously shown the presence of the pertussis toxin-sensitive G _i-3 protein on Golgi membranes and demonstrated a functional role for G _i-3 in the trafficking of secretory proteins through the Golgi complex. We have also described a brefeldin A-sensitive phosphoprotein, p200, which is found in the cytoplasm and on Golgi membranes. The present study investigates the role of heterotrimeric G proteins in the regulation of p200 binding to Golgi membranes. An in vitro binding assay was used to measure the binding of cytosolic p200 to LLC-PK₁ cell microsomal membranes and to purified rat liver Golgi membranes in the presence of specific activators of G proteins. The binding of p200 to Golgi membranes was compared to that of the coatomer protein-COP, for which G protein-dependent membrane binding has previously been established. Membrane binding of both p200 and-COP was induced maxi-mally by activation of all G proteins in the presence of GTP S. More selective activation of the heterotrimeric G proteins, with AlFn or mastoparan, also induced membrane binding of p200 and-COP. Pertussis toxin pretreatment of Golgi membranes, to selectively inacti-vate G _i-3, reduced the AlFn and mastoparan-induced binding of p200 to Golgi membranes, whereas no sig-nificant effect of pertussis toxin on-COP binding was found in this assay. The effect of pertussis toxin thus implicates G _i-3, as one component of a regulatory path-way, in the binding of cytosolic p200 to Golgi mem-branes. The effects of AlFn and pertussis toxin on p200 membrane binding were also shown in intact cells by immunofluorescence staining. AlFn treatment of cells induced translocation of p200 from the cytoplasm onto the Golgi complex, resulting in a conformational change in some Golgi membranes. The translocation of p200 was blocked by pretreatment of intact NRK cells with pertussis toxin. The data presented here support the conclusion that the binding of the p200 protein to Golgi membranes involves regulation by the pertussis toxin-sensitive heterotrimeric G proteins, specifically the G _i-3 protein.