ArhGAP15, a Rac-specific GTPase-activating Protein,Plays a Dual Role in Inhibiting Small GTPase Signaling |
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Authors: | Maria Radu Sonali J. Rawat Alexander Beeser Anton Iliuk Weiguo Andy Tao Jonathan Chernoff |
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Affiliation: | From the ‡Cancer Biology Program, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.;the §Department of Biochemistry and Molecular Biology, Drexel University, Philadelphia, Pennsylvania 19102, and ;the ¶Department of Biochemistry, Purdue University, West Lafayette, Indiana 47907 |
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Abstract: | Signaling from small GTPases is a tightly regulated process. In this work we used a protein microarray screen to identify the Rac-specific GAP, ArhGAP15, as a substrate of the Rac effectors Pak1 and Pak2. In addition to serving as a substrate of Pak1/2, we found that ArhGAP15, via its PH domain, bound to these kinases. The association of ArhGAP15 to Pak1/2 resulted in mutual inhibition of GAP and kinase catalytic activity, respectively. Knock-down of ArhGAP15 resulted in activation of Pak1/2, both indirectly, as a result of Rac activation, and directly, as a result of disruption of the ArhGAP15/Pak complex. Our data suggest that ArhGAP15 plays a dual negative role in regulating small GTPase signaling, by acting at the level of the GTPase itself, as well interacting with its effector, Pak kinase. |
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Keywords: | ERK Protein Kinases Protein Phosphorylation Signal Transduction Small GTPases |
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