Publication | Open Access
Aurora-A Phosphorylates, Activates, and Relocalizes the Small GTPase RalA
117
Citations
56
References
2009
Year
CytoskeletonCellular PhysiologyTumor BiologySignaling PathwayCell RegulationReceptor Tyrosine KinaseAutophagySmall Gtpase RalaSmall Gtpase RasRadiation OncologyCell SignalingCell BiologySignal TransductionOncogenic RasKinase Aurora-aTumor SuppressorIntracellular TraffickingCellular BiochemistryMedicine
The small GTPase Ras, which transmits extracellular signals to the cell, and the kinase Aurora-A, which promotes proper mitosis, can both be inappropriately activated in human tumors. Here, we show that Aurora-A in conjunction with oncogenic Ras enhances transformed cell growth. Furthermore, such transformation and in some cases also tumorigenesis depend upon S194 of RalA, a known Aurora-A phosphorylation site. Aurora-A promotes not only RalA activation but also translocation from the plasma membrane and activation of the effector protein RalBP1. Taken together, these data suggest that Aurora-A may converge upon oncogenic Ras signaling through RalA.
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