Abstract
Protein kinases play a pivotal role in execution of cell division. Polo and Polo-like kinases have emerged as major regulators for various cell cycle checkpoints. Early genetic studies have demonstrated that CDC5, a budding yeast counterpart of vertebrate Plks, is essential for successful mitotic progression. Mammalian Plks localize primarily to the centrosome during interphase and the mitotic apparatus during mitosis. Many key cell cycle regulators such as p53, Cdc25C, cyclin B, components of the anaphase-promoting complex, and mitotic motor proteins are directly targeted by Plks. Although the exact mechanism of action of these protein kinases in vivo remains to be elucidated, Plks are important mediators for various cell cycle checkpoints that monitor centrosome duplication, DNA replication, formation of bipolar mitotic spindle, segregation of chromosomes, and mitotic exit, thus protecting cells against genetic instability during cell division.
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Acknowledgements
We apologize to many authors whose articles could not be cited in this review due to space limitations. We thank Dr Frank Traganos for critical reading of the manuscript and the members in Dr Dai's laboratory for helpful discussions. We also thank Ms Lisa Buerle for editorial and administrative assistance. The work is supported in part by grants from the National Institutes of Health to WD (CA90658 and CA74229) and to ML (GM31973).
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Xie, S., Xie, B., Lee, M. et al. Regulation of cell cycle checkpoints by polo-like kinases. Oncogene 24, 277–286 (2005). https://doi.org/10.1038/sj.onc.1208218
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DOI: https://doi.org/10.1038/sj.onc.1208218
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