Abstract
During mitosis, chromosome alignment depends on the regulated dynamics of microtubules and on motor protein activities. At the kinetochore, the interplay between microtubule-binding proteins, motors, and kinases is poorly understood. Cenp-E is a kinetochore-associated kinesin involved in chromosome congression, but the mechanism by which this is achieved is unclear. Here, we present a study of the regulation of Cenp-E motility by using purified full-length (FL) Xenopus Cenp-E protein, which demonstrates that FL Cenp-E is a genuine plus-end-directed motor. Furthermore, we find that the Cenp-E tail completely blocks the motility of Cenp-E in vitro. This is achieved through direct interaction between its motor and tail domains. Finally, we show that Cenp-E autoinhibition is reversed by MPS1- or CDK1-cyclin B-mediated phosphorylation of the Cenp-E tail. This suggests a model of dynamic control of Cenp-E motility, and hence chromosome congression, dependent upon phosphorylation at the kinetochore. © 2008 Elsevier Inc. All rights reserved.
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CITATION STYLE
Espeut, J., Gaussen, A., Bieling, P., Morin, V., Prieto, S., Fesquet, D., … Abrieu, A. (2008). Phosphorylation Relieves Autoinhibition of the Kinetochore Motor Cenp-E. Molecular Cell, 29(5), 637–643. https://doi.org/10.1016/j.molcel.2008.01.004
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