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Nek2蛋白激酶的底物特异性和细胞周期调控,Nek2蛋白激酶可能是构巢曲霉有丝分裂调节因子NIMA的人类同源物。

Substrate specificity and cell cycle regulation of the Nek2 protein kinase, a potential human homolog of the mitotic regulator NIMA of Aspergillus nidulans.

作者信息

Fry A M, Schultz S J, Bartek J, Nigg E A

机构信息

Swiss Institute for Experimental Cancer Research (ISREC), Epalinges.

出版信息

J Biol Chem. 1995 May 26;270(21):12899-905. doi: 10.1074/jbc.270.21.12899.

DOI:10.1074/jbc.270.21.12899
PMID:7759549
Abstract

The human Nek2 protein kinase is the closest known mammalian relative of the mitotic regulator NIMA of Aspergillus nidulans. The two kinases share 47% sequence identity over their catalytic domains and display a similar cell cycle-dependent expression peaking at the G2 to M phase transition. Hence, it is attractive to speculate that human Nek2 and fungal NIMA may carry out similar functions at the onset of mitosis. To study the biochemical properties and substrate specificity of human Nek2 and compare them to those reported previously for other NIMA-related protein kinases, we have expressed Nek2 in insect cells. We show that recombinant Nek2 is active as a serine/threonine-specific protein kinase and may undergo autophosphorylation. Both human Nek2 and fungal NIMA phosphorylate a similar, albeit not identical, set of proteins and synthetic peptides, and beta-casein was found to be a suitable substrate for assaying Nek2 in vitro. By exploiting these findings, we have studied the cell cycle regulation of Nek2 activity in HeLa cells. We show that Nek2 activity parallels its abundance, being low during M and G1 but high during S and G2 phase. Taken together, our results suggest that human Nek2 resembles fungal NIMA in its primary structure, cell cycle regulation of expression, and substrate specificity, but that Nek2 may function earlier in the cell cycle than NIMA.

摘要

人类Nek2蛋白激酶是已知与构巢曲霉有丝分裂调节因子NIMA亲缘关系最近的哺乳动物蛋白激酶。这两种激酶在其催化结构域上有47%的序列一致性,并且在细胞周期依赖性表达上相似,在G2到M期转换时达到峰值。因此,推测人类Nek2和真菌NIMA在有丝分裂开始时可能执行相似功能很有吸引力。为了研究人类Nek2的生化特性和底物特异性,并将它们与先前报道的其他NIMA相关蛋白激酶的特性进行比较,我们在昆虫细胞中表达了Nek2。我们发现重组Nek2作为一种丝氨酸/苏氨酸特异性蛋白激酶具有活性,并且可能发生自磷酸化。人类Nek2和真菌NIMA都磷酸化一组相似但不完全相同的蛋白质和合成肽,并且发现β-酪蛋白是体外检测Nek2的合适底物。利用这些发现,我们研究了HeLa细胞中Nek2活性的细胞周期调控。我们发现Nek2活性与其丰度平行,在M期和G1期低,但在S期和G2期高。综上所述,我们的结果表明,人类Nek2在一级结构、表达的细胞周期调控和底物特异性方面类似于真菌NIMA,但Nek2可能在细胞周期中比NIMA更早发挥作用。

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