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Vol. 17, Issue 10, 4390-4399, October 2006
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Department of Biological Sciences, Stanford University, Stanford, CA 94305-5020
Submitted April 24, 2006;
Revised July 18, 2006;
Accepted July 21, 2006
Monitoring Editor: Yixian Zheng
Accurate chromosome segregation is controlled by the spindle checkpoint, which responds to the lack of microtubule–kinetochore attachment or of tension across sister kinetochores through phosphorylation of kinetochore proteins by the Mps1, Bub1, BubR1, Aurora B, and Plk1/Plx1 kinases. The presence of the 3F3/2 phosphoepitope on kinetochores, generated by Plk1/Plx1-mediated phosphorylation of an unknown protein, correlates with the activation of the tension-sensitive checkpoint pathway. Using immunodepletion approach and a rephosphorylation assay in Xenopus extracts, we report here that not only the formation of the 3F3/2 phosphoepitope is dependent on the checkpoint activation but also the loading of the 3F3/2 substrate to kinetochores requires the prior assembly of Mps1, Bub1 and BubR1 onto kinetochores. Interestingly, generation of the 3F3/2 epitope in checkpoint extracts requires the kinase activities of Mps1 and Bub1 but not that of BubR1. Furthermore, we demonstrate that checkpoint proteins in Xenopusextracts are assembled onto kinetochores in a highly ordered pathway consisting of three steps. Mps1 and Bub1 are loaded first, and BubR1 and Plx1 second, followed by Mad1 and Mad2. The characterization of this ordered assembly pathway provides a framework for the biochemical mechanism of the checkpoint signaling and will aid in the eventual identification of the 3F3/2 substrate.
Address correspondence to: Guowei Fang (gwfang{at}stanford.edu)
Abbreviations used: Plk1/Plx1, Polo-like kinase 1.
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