Controlling the cell cycle The role of calcium/calmodulin-stimulated protein kinases I and II

被引:79
作者
Skelding, Kathryn A. [1 ]
Rostas, John A. P.
Verrills, Nicole M.
机构
[1] Univ Newcastle, Sch Biomed Sci & Pharm, Fac Hlth, Callaghan, NSW 2308, Australia
基金
英国医学研究理事会;
关键词
calcium/calmodulin; protein phosphorylation; CaMKII; CaMKI; cell cycle; KN-93; KN-62; SUPPRESSES TUMOR-GROWTH; MOUSE EGG ACTIVATION; INTRACELLULAR CALCIUM; ANAPHASE TRANSITION; MEIOTIC MATURATION; INHIBITOR PROTEIN; MOLECULAR-CLONING; ALPHA-CAMKII; CALMODULIN; PHOSPHORYLATION;
D O I
10.4161/cc.10.4.14798
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Many studies have implicated Ca2+ and calmodulin (CaM) as regulators of the cell cycle. Ca2+/CaM-stimulated proteins, including the family of multifunctional Ca2+/CaM-stimulated protein kinases (CaMK), have also been identified as mediators of cell cycle progression. CaMKII is the best-characterized member of this family, and is regulated by multi-site phosphorylation and targeting. Using pharmacological inhibitors that were believed to be specific for CaMKII, CaMKII has been implicated in every phase of the cell cycle. However, these 'specific' inhibitors also produce effects on other CaMKs. These additional effects are usually ignored, and the effects of the inhibitors are normally attributed to CaMKII without further investigation. Using new specific molecular techniques, it has become clear that CaMKI is an important regulator of G(1), whereas CaMKII is essential for regulating G(2)/M and the metaphase-anaphase transition. If the mechanisms controlling these events can be fully elucidated, new targets for controlling proliferative diseases may be identified.
引用
收藏
页码:631 / 639
页数:9
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