Identification and characterization of potential effector molecules of theRas-related GTPase Rap2

In search for effecters of the Ras-related GTPase Rapa, we used the yeast t wo-hybrid method and identified the C-terminal Ras/Rap interaction domain o f the Ral exchange factors (RalGEFs) Ral GDP dissociation stimulator (RalGD S), RalGDS-like (RGL), and RalGDS-like factor (Rlf), These proteins, which also interact with activated Ras and Rap1, are effecters of Ras and mediate the activation of Ral in response to the activation of Ras. Here we show t hat the full-length RalGEFs interact with the GTP-bound form of Rap2 in the two-hybrid system as well as in vitro. When co-transfected in HeLa cells, an activated Rapa mutant (Rap2Val-12) but not an inactive protein (Rap2Ala- 35) co-immunoprecipitates with RalGDS and Rlf; moreover, Rap2-RalGEF comple xes can be isolated from the particulate fraction of transfected cells and were localized by confocal microscopy to the resident compartment of Rap2, i.e. the endoplasmic reticulum. However, the overexpression of activated Ra p2 neither leads to the activation of the Ral GTPase via RalGEFs nor inhibi ts Ras-dependent Ral activation in vivo. Several hypotheses that could expl ain these results, including compartmentalization of proteins involved in s ignal transduction, are discussed. Our results suggest that in cells, the i nteraction of Rap2 with RalGEFs might trigger other cellular responses than activation of the Ral GTPase.