Rac GTPase instructs NF-kB activation by conveying the SCF complex and IkBα to the ruffling membranes

NF-kB is an ubiquitously expressed transcription factor that plays a central role in directing a vast range of cellular functions. Its activation is controlled by the Rac GTPase and relies on the coordinated cooperation of the E3-ligase complex SCF βTrCP , composed by Skp-1/Cullin-1, Rbx/Roc1 and the β−TrCP proteins. Recently, Cullin-1 has been reported to form a complex with the activated Rac GTPase. Here we show that the specific activation of the Rac GTPase, besides directing its own positioning, induces the re-localization of the SCF component Cullin-1 to the ruffling membranes. This occurred only if the ruffles were stimulated by the Rac GTPase and was accompanied by the repositioning to the same intracellular compartment of the SCF protein Skp-1 and the ubiquitin-like molecule Nedd-8. The SCF substrate IkBα was also directed to the ruffling membranes in a Rac-dependent way. The novelty of these findings is in respect to the demonstration that the correct positioning at the ruffling membranes is crucial for the subsequent series of events that leads to IkBα proteasomal degradation and the resultant activation of NF-kB. Consequently, this points to the role of Rac as a docking molecule in NF-kB activation.