Identification of Proteins That Interact with the Central Coiled-Coil Region of the Human Protein Kinase NEK1

生物 激酶 丝氨酸苏氨酸激酶 细胞生物学 遗传学 多囊肾病 细胞周期蛋白 有丝分裂 细胞周期 蛋白激酶A cDNA文库 互补DNA 细胞 基因 肾
作者
Marcelo J. Surpili,Tatiana M. Delben,Jörg Kobarg
出处
期刊:Biochemistry [American Chemical Society]
卷期号:42 (51): 15369-15376 被引量:85
标识
DOI:10.1021/bi034575v
摘要

NEK protein kinases are evolutionarily conserved kinases structurally related to the Aspergillus nidulans mitotic regulator NIMA. At least nine members of the NEK family in vertebrates have been described to date, but for most of them the interacting protein partners are unknown. The pleiotropic deleterious effects and the formation of kidney cysts caused by NEK1 mutation in mice emphasize its involvement in the regulation of diverse cellular processes and in the etiology of polycystic kidney disease (PKD), respectively. Here we report the identification of proteins that interacted with the human NEK1 protein kinase in a yeast two-hybrid screen of a human fetal brain cDNA library, using the catalytic and regulatory domains of NEK1 separately as baits. These proteins are known to take part either in the development of PKD, in the double-strand DNA break repair at the G2/M transition phase of the cell cycle, or in neural cell development. The proteins involved in PKD include the motor protein KIF3A and the proteins tuberin and α-catulin. Mapping studies of the human NEK1 regulatory domain (NRD) indicated a strong interaction of most of the proteins retrieved from the library with putative coiled coils located in the central region of NRD. Our results give further support to the previous observation that NEK1 is of functional importance for the etiology of PKD.
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