[KSCI] Korea Science Citation Index Service

http://dx.doi.org/10.5483/BMBRep.2013.46.6.041

PP2A function toward mitotic kinases and substrates during the cell cycle

Jeong, Ae Lee (Center for Women's Disease, Department of Biological Science, Sookmyung Women's University)
Yang, Young (Center for Women's Disease, Department of Biological Science, Sookmyung Women's University)

Publication Information

BMB Reports / v.46, no.6, 2013 , pp. 289-294 More about this Journal

Abstract

To maintain cellular homeostasis against the demands of the extracellular environment, a precise regulation of kinases and phosphatases is essential. In cell cycle regulation mechanisms, activation of the cyclin-dependent kinase (CDK1) and cyclin B complex (CDK1:cyclin B) causes a remarkable change in protein phosphorylation. Activation of CDK1:cyclin B is regulated by two auto-amplification loops-CDK1:cyclin B activates Cdc25, its own activating phosphatase, and inhibits Wee1, its own inhibiting kinase. Recent biological evidence has revealed that the inhibition of its counteracting phosphatase activity also occurs, and it is parallel to CDK1:cyclin B activation during mitosis. Phosphatase regulation of mitotic kinases and their substrates is essential to ensure that the progression of the cell cycle is ordered. Outlining how the mutual control of kinases and phosphatases governs the localization and timing of cell division will give us a new understanding about cell cycle regulation.

Keywords

Aurora B; CDK1:cyclin B; Cell cycle; PLK1; PP2A;

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Times Cited By KSCI : 1 (Citation Analysis)

Reference
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