Xiao G, Harhaj E W, Sun S C
Department of Microbiology and Immunology, Pennsylvania State University College of Medicine, Hershey, Pennsylvania 17033, USA.
J Biol Chem. 2000 Nov 3;275(44):34060-7. doi: 10.1074/jbc.M002970200.
The human T-cell leukemia virus type 1 Tax oncoprotein deregulates the NF-kappa B signaling pathway by persistently stimulating a key signal transducer, the I kappa B kinase (IKK). Tax physically associates with the IKK regulatory subunit, IKK gamma, although the underlying biochemical mechanism and functional significance remain unclear. We show that the Tax-IKK gamma interaction requires two homologous leucine zipper domains located within IKK gamma. These leucine zipper domains are unique for the presence of a conserved upstream region that is essential for Tax binding. Site-directed mutagenesis analysis revealed that a leucine-repeat region of Tax is important for IKK gamma binding. Interestingly, all the Tax mutants defective in IKK gamma binding failed to engage the IKK complex or stimulate IKK activity, and these functional defects can be rescued by fusing the Tax mutants to IKK gamma. These results provide mechanistic insights into how Tax specifically targets and functionally activates the cellular kinase IKK.
人类1型T细胞白血病病毒Tax癌蛋白通过持续刺激关键信号转导分子IκB激酶(IKK)来失调NF-κB信号通路。Tax与IKK调节亚基IKKγ发生物理性结合,尽管其潜在的生化机制和功能意义仍不清楚。我们发现Tax与IKKγ的相互作用需要IKKγ内的两个同源亮氨酸拉链结构域。这些亮氨酸拉链结构域因存在对Tax结合至关重要的保守上游区域而独特。定点诱变分析表明Tax的一个亮氨酸重复区域对IKKγ结合很重要。有趣的是,所有在IKKγ结合方面有缺陷的Tax突变体都无法与IKK复合物结合或刺激IKK活性,并且通过将Tax突变体与IKKγ融合可挽救这些功能缺陷。这些结果为Tax如何特异性靶向并功能性激活细胞激酶IKK提供了机制性见解。