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Vol. 18, Issue 9, 3264-3276, September 2007
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*Department of Biology, Indiana University, Bloomington, IN 47405;
Department of Biochemistry and Molecular Genetics, University of Virginia Medical School, Charlottesville, VA 22908; and
Department of Biochemistry and Molecular Biology, Indiana University Medical Sciences, Bloomington, IN 47405
Submitted February 1, 2007;
Revised May 24, 2007;
Accepted June 5, 2007
Monitoring Editor: Ted Salmon
Chromosome congression and segregation require the proper attachment of microtubules to the two sister kinetochores. Disruption of either Aurora B kinase or the Kinesin-13 mitotic centromere-associated kinesin (MCAK) increases chromosome misalignment and missegregation due to improper kinetochore–microtubule attachments. MCAK localization and activity are regulated by Aurora B, but how Aurora B phosphorylation of MCAK affects spindle assembly is unclear. Here, we show that the binding of MCAK to chromosome arms is also regulated by Aurora B and that Aurora B-dependent chromosome arm and centromere localization is regulated by distinct two-site phosphoregulatory mechanisms. MCAK association with chromosome arms is promoted by phosphorylation of T95 on MCAK, whereas phosphorylation of S196 on MCAK promotes dissociation from the arms. Although targeting of MCAK to centromeres requires phosphorylation of S110 on MCAK, dephosphorylation of T95 on MCAK increases the binding of MCAK to centromeres. Our study reveals a new role for Aurora B, which is to prevent excess MCAK binding to chromatin to facilitate chromatin-nucleated spindle assembly. Our study also shows that the interplay between multiple phosphorylation sites of MCAK may be critical to temporally and spatially control MCAK function.
The online version of this article contains supplemental material at MBC Online (http://www.molbiolcell.org).
Address correspondence to: Claire E. Walczak (cwalczak{at}indiana.edu).
Abbreviations used: GFP, green fluorescent protein; MT, microtubule; PAGE, polyacrylamide gel electrophoresis.
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