Mitotic Regulation by NEK Kinase Networks

被引:72
作者
Fry, Andrew M. [1 ]
Bayliss, Richard [2 ]
Roig, Joan [3 ]
机构
[1] Univ Leicester, Dept Mol & Cell Biol, Leicester, Leics, England
[2] Univ Leeds, Sch Mol & Cellular Biol, Leeds, W Yorkshire, England
[3] CSIC, IBMB, Barcelona, Spain
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
protein kinase; mitosis; microtubule; centrosome; cilia; NIMA-RELATED KINASE; CENTROSOMAL PROTEIN C-NAP1; CYSTIC KIDNEY-DISEASE; CELL-CYCLE REGULATION; COILED-COIL PROTEIN; DNA-DAMAGE; FAMILY KINASE; SUBSTRATE-SPECIFICITY; CANDIDATE SUBSTRATE; NLRP3; ACTIVATION;
D O I
10.3389/fcell.2017.00102
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Genetic studies in yeast and Drosophila led to identification of cyclin-dependent kinases (CDKs), Polo-like kinases (PLKs) and Aurora kinases as essential regulators of mitosis. These enzymes have since been found in the majority of eukaryotes and their cell cycle-related functions characterized in great detail. However, genetic studies in another fungal species, Aspergillus nidulans, identified a distinct family of protein kinases, the NEKs, that are also widely conserved and have key roles in the cell cycle, but which remain less well studied. Nevertheless, it is now clear that multiple NEK family members act in networks to regulate specific events of mitosis, including centrosome separation, spindle assembly and cytokinesis. Here, we describe our current understanding of how the NEK kinases contribute to these processes, particularly through targeted phosphorylation of proteins associated with the microtubule cytoskeleton. We also present the latest findings on molecular events that control the activation state of the NEKs and how these are revealing novel modes of enzymatic regulation relevant not only to other kinases but also to pathological mechanisms of disease.
引用
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页数:13
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