Qin C L, Tang J, Kim K
Department of Medicine (Division of Infectious Diseases), Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Mol Biochem Parasitol. 1998 Jun 1;93(2):273-83. doi: 10.1016/s0166-6851(98)00042-5.
As an initial effort to dissect the signaling pathways responsible for pathogenesis of Toxoplasma gondii infection, we report the cloning and in vitro functional studies of TPK3 (Toxoplasma protein kinase-3), a homologue of shaggy/glycogen synthase kinase-3 (GSK-3) kinases. The shaggy/GSK-3 family of kinases are highly conserved protein kinases that play important roles in cell fate determination, nuclear signaling and hormonal regulation. The TPK3 gene was isolated by RT-PCR with degenerate primers corresponding to highly conserved regions of serine/threonine protein kinases. The complete sequences of genomic and cDNA clones indicated the open reading frame, 1185 bp in size, is interrupted by five introns. The predicted protein sequence of TPK3 shows 54% identity to shaggy/GSK-3 over the catalytic domains. Southern analysis revealed TPK3 is a single copy locus in the Toxoplasma genome. Antisera to other GSK-3 proteins from other species recognized GST-TPK3 and a protein of the predicted size in parasites lysates. In vitro kinase assays with GST-TPK3 indicated that TPK3 autophosphorylates and phosphorylates protein phosphatase inhibitor-2 (I-2), a specific substrate of GSK-3 kinase.
作为剖析弓形虫感染发病机制相关信号通路的初步尝试,我们报告了TPK3(弓形虫蛋白激酶-3)的克隆及体外功能研究,TPK3是一种与shaggy/糖原合酶激酶-3(GSK-3)同源的激酶。shaggy/GSK-3激酶家族是高度保守的蛋白激酶,在细胞命运决定、核信号传导和激素调节中发挥重要作用。通过RT-PCR,使用对应于丝氨酸/苏氨酸蛋白激酶高度保守区域的简并引物分离出TPK3基因。基因组和cDNA克隆的完整序列表明,大小为1185 bp的开放阅读框被5个内含子打断。TPK3的预测蛋白序列在催化结构域与shaggy/GSK-3显示出54%的同一性。Southern分析表明TPK3是弓形虫基因组中的单拷贝基因座。来自其他物种的针对其他GSK-3蛋白的抗血清识别GST-TPK3以及寄生虫裂解物中预测大小的蛋白。用GST-TPK3进行的体外激酶分析表明,TPK3可自身磷酸化并磷酸化蛋白磷酸酶抑制剂-2(I-2),I-2是GSK-3激酶的特异性底物。