Kimura M, Matsuda Y, Yoshioka T, Okano Y
Department of Molecular Pathobiochemistry, Gifu University School of Medicine, Tsukasamachi-40, Gifu 500-8705, Japan.
J Biol Chem. 1999 Mar 12;274(11):7334-40. doi: 10.1074/jbc.274.11.7334.
We earlier isolated cDNAs encoding novel human protein kinases AIK and AIK2 sharing high amino acid sequence identities with Drosophila Aurora and Saccharomyces cerevisiae Ipl1 kinases whose mutations cause abnormal chromosome segregation. In the present study, a third human cDNA (AIK3) highly homologous to aurora/IPL1 was isolated, and the nucleotide sequence was determined. This cDNA encodes 309 amino acids with a predicted molecular mass of 35.9 kDa. C-terminal kinase domain of AIK3 protein shares high amino acid sequence identities with those of Aurora/Ipl1 family protein kinases including human AIK, human AIK2, Xenopus pEg2, Drosophila Aurora, and yeast Ipl1, whereas the N-terminal domain of AIK3 protein shares little homology with any other Aurora/Ipl1 family members. AIK3 gene was assigned to human chromosome 19q13.43, which is a frequently deleted or rearranged region in several tumor tissues, by fluorescence in situ hybridization, somatic cell hybrid panel, and radiation hybrid cell panel. Northern blot analyses revealed that AIK3 expression was limited to testis. The expression levels of AIK3 in several cancer cell lines were elevated severalfold compared with normal fibroblasts. In HeLa cells, the endogenous AIK3 protein level is low in G1/S, accumulates during G2/M, and reduces after mitosis. Immunofluorescence studies using a specific antibody have shown that AIK3 is localized to centrosome during mitosis from anaphase to cytokinesis. These results suggest that AIK3 may play a role(s) in centrosome function at later stages of mitosis.
我们之前分离出了编码新型人类蛋白激酶AIK和AIK2的cDNA,它们与果蝇极光激酶和酿酒酵母Ipl1激酶具有高度的氨基酸序列同一性,其突变会导致异常的染色体分离。在本研究中,我们分离出了与极光/IPL1高度同源的第三个人类cDNA(AIK3),并测定了其核苷酸序列。该cDNA编码309个氨基酸,预测分子量为35.9 kDa。AIK3蛋白的C末端激酶结构域与极光/Ipl1家族蛋白激酶(包括人类AIK、人类AIK2、非洲爪蟾pEg2、果蝇极光激酶和酵母Ipl1)的C末端激酶结构域具有高度的氨基酸序列同一性,而AIK3蛋白的N末端结构域与其他任何极光/Ipl1家族成员几乎没有同源性。通过荧光原位杂交、体细胞杂交板和辐射杂交细胞板,将AIK3基因定位于人类染色体19q13.43,该区域在几种肿瘤组织中经常发生缺失或重排。Northern印迹分析显示AIK3的表达仅限于睾丸。与正常成纤维细胞相比,几种癌细胞系中AIK3的表达水平提高了几倍。在HeLa细胞中,内源性AIK3蛋白水平在G1/S期较低,在G2/M期积累,并在有丝分裂后降低。使用特异性抗体进行的免疫荧光研究表明,AIK3在有丝分裂后期到胞质分裂期间定位于中心体。这些结果表明,AIK3可能在有丝分裂后期的中心体功能中发挥作用。