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Polo-like kinase 1 regulates the stability of the mitotic centromere-associated kinesin in mitosis

Belsham, Hannah R.; Friel, Claire T.; Sanhaji, Mourad; Ritter, Andreas; Belsham, Hannah; Roth, Susanne; Louwen, Frank; Yuan, Juping

Authors

Hannah R. Belsham

Mourad Sanhaji

Andreas Ritter

Hannah Belsham

Susanne Roth

Frank Louwen

Juping Yuan



Abstract

Proper bi-orientation of chromosomes is critical for the accurate segregation of chromosomes in mitosis. A key regulator of this process is MCAK, the mitotic centromere-associated kinesin. During mitosis the activity and localization of MCAK are regulated by mitotic key kinases including Plk1 and Aurora B. We show here that S621 in the MCAK's C-terminal domain is the major phosphorylation site for Plk1. This phosphorylation regulates MCAK's stability and facilitates its recognition by the ubiquitin/proteasome dependent APC/CCdc20 pathway leading to its D-box dependent degradation in mitosis. While phosphorylation of S621 does not directly affect its microtubule depolymerising activity, loss of Plk1 phosphorylation on S621 indirectly enhances its depolymerization activity in vivo by stabilizing MCAK, leading to an increased level of protein. Interfering with phosphorylation at S621 causes spindle formation defects and chromosome misalignments. Therefore, this study suggests a new mechanism by which Plk1 regulates MCAK: by regulating its degradation and hence controlling its turnover in mitosis. © 2008-2014 Impact Journals, LLC.

Citation

Belsham, H. R., Friel, C. T., Sanhaji, M., Ritter, A., Belsham, H., Roth, S., …Yuan, J. (2014). Polo-like kinase 1 regulates the stability of the mitotic centromere-associated kinesin in mitosis. Oncotarget, 5(10), 3130-3144. https://doi.org/10.18632/oncotarget.1861

Journal Article Type Article
Acceptance Date Mar 24, 2014
Online Publication Date Mar 24, 2014
Publication Date Mar 24, 2014
Deposit Date Jun 14, 2018
Journal Oncotarget
Electronic ISSN 1949-2553
Publisher Impact Journals
Peer Reviewed Peer Reviewed
Volume 5
Issue 10
Pages 3130-3144
DOI https://doi.org/10.18632/oncotarget.1861
Public URL https://nottingham-repository.worktribe.com/output/1117877
PMID 24931513