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PMID: 15640846 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

The Plk3-Cdc25 circuit.

Oncogene ·Vol. 24 ·No. 2 ·2005-01-10 ·Pages 299-305

Myer DL, Bahassi el M, Stambrook PJ

Abstract

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.

MeSH Terms
Animals Cell Cycle Proteins/physiology Humans Mitosis/physiology Protein Serine-Threonine Kinases/physiology Tumor Suppressor Proteins Xenopus Proteins/physiology cdc25 Phosphatases/physiology
Chemicals
Cell Cycle Proteins Tumor Suppressor Proteins Xenopus Proteins PLK3 protein, Xenopus PLK3 protein, human Plk3 protein, rat Plk3 protein, mouse Protein Serine-Threonine Kinases CDC25A protein, human CDC25C protein, human Cdc25a protein, mouse Cdc25a protein, rat Cdc25c protein, mouse cdc25 Phosphatases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Myer David L
Department of Cell Biology, Neurobiology and Anatomy, University of Cincinnati College of Medicine, 3125 Eden Avenue, Cincinnati, OH 45267, USA.
Bahassi El Mustapha
Stambrook Peter J
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
2005-01-10
Pages
299-305
Language
English
Region
England
NLM ID
8711562
Subset
IM
Grants
NIEHS NIH HHS · P30 ES05652 · United States
NIEHS NIH HHS · P30-ES06096 · United States
NCI NIH HHS · R01 CA90934 · United States
NIEHS NIH HHS · T32 ES07250 · United States
NIEHS NIH HHS · U01 ES011038 · United States
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