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Originally published as MBC in Press, 10.1091/mbc.E02-02-0092 on July 11, 2002
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Vol. 13, Issue 9, 3064-3077, September 2002

Aurora B Kinase Exists in a Complex with Survivin and INCENP and Its Kinase Activity Is Stimulated by Survivin Binding and Phosphorylation

Margaret A. Bolton,* Weijie Lan,* Shannon E. Powers,* Mark L. McCleland,* Jian Kuang,dagger and P. Todd Stukenberg*Dagger

 *Department of Biochemistry and Molecular Genetics, University of Virginia Medical Center, Charlottesville, Virginia 22908; and  dagger Department of Experimental Therapeutics, University of Texas, MD Anderson Center, Houston, Texas 77908

Aurora B regulates chromosome segregation and cytokinesis and is the first protein to be implicated as a regulator of bipolar attachment of spindle microtubules to kinetochores. Evidence from several systems suggests that Aurora B is physically associated with inner centromere protein (INCENP) in mitosis and has genetic interactions with Survivin. It is unclear whether the Aurora B and INCENP interaction is cell cycle regulated and if Survivin physically interacts in this complex. In this study, we cloned the Xenopus Survivin gene, examined its association with Aurora B and INCENP, and determined the effect of its binding on Aurora B kinase activity. We demonstrate that in the Xenopus early embryo, all of the detectable Survivin is in a complex with both Aurora B and INCENP throughout the cell cycle. Survivin and Aurora B bind different domains on INCENP. Aurora B activity is stimulated >10-fold in mitotic extracts; this activation is phosphatase sensitive, and the binding of Survivin is required for full Aurora B activity. We also find the hydrodynamic properties of the Aurora B/Survivin/INCENP complex are cell cycle regulated. Our data indicate that Aurora B kinase activity is regulated by both Survivin binding and cell cycle-dependent phosphorylation.


Dagger Corresponding author. E-mail address: pts7h{at}virginia.edu.


Molecular Biology of the Cell
Vol. 13, 3064-3077, September 2002
Copyright © 2002 by The American Society for Cell Biology



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