4.8 Article

The Plk3-Cdc25 circuit

Journal

ONCOGENE
Volume 24, Issue 2, Pages 299-305

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/sj.onc.1208278

Keywords

Polo-like kinases; Cdc25 phosphatases; phosphorylation; cell-cycle regulation

Funding

  1. NCI NIH HHS [R01 CA90934] Funding Source: Medline
  2. NIEHS NIH HHS [U01 ES011038, P30-ES06096, T32 ES07250, P30 ES05652] Funding Source: Medline

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Polo-like kinases (Plks) are key regulators of the cell cycle, especially in the G2 phase and mitosis. They are incorporated into signaling networks that regulate many aspects of the cell cycle, including but not limited to centrosome maturation and separation, mitotic entry, chromosome segregation, mitotic exit, and cytokinesis. The Plks have well conserved 30-amino-acid elements, designated polo boxes (PBs), located in their carboxyl-termini, which with their flanking regions constitute a functional Polo-box domain (PBD). Members of the Plk family exist in a variety of organisms including Polo in Drosophila melanogaster; Cdc5 in Saccharomyces cerevisiae; Plo1 in Schizosaccharomyces pombe; Plx1 in Xenopus laevis; and Plk1, Snk/Plk2, Fnk/Prk/Plk3, and Sak in mammals. Polo, Cdc5, and Plo1 are essential for viability. The Plks can be separated into two groups according to their functions. The first group ( Polo, Cdc5, plo1, Plx1, and Plk1) primarily performs mitotic functions, whereas the second group (Plk2 and Plk3) appears to have additional functions during the G1, S, and G2 phases of the cell cycle. Several contributions to this issue will discuss different aspects of Plk involvement in cell-cycle regulation. This review, therefore, will focus on the role of Plk3 in regulating Cdc25 phosphatase function and its effect on the cell cycle.

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