Sakurai H, Shigemori N, Hasegawa K, Sugita T
Lead Generation Research Laboratory, Tanabe Seiyaku Co., Ltd., Osaka, Japan.
Biochem Biophys Res Commun. 1998 Feb 13;243(2):545-9. doi: 10.1006/bbrc.1998.8124.
Several mitogen-activated protein kinase kinase kinases (MAPKKKs), including NF-kappa B-inducing kinase (NIK), play critical roles in NF-kappa B activation. We isolated cDNA for human TGF-beta activated kinase 1 (TAK1), a member of the MAPKKK family, and evaluated its ability to stimulate NF-kappa B activation. Overexpression of TAK1 together with its activator protein, TAK1 binding protein 1 (TAB1), induced the nuclear translocation of NF-kappa B p50/p65 heterodimer accompanied by the degradation of I kappa B alpha and I kappa B beta, and the expression of kappa B-dependent reporter gene. A dominant negative mutant of NIK did not inhibit TAK1-induced NF-kappa B activation. These results suggest that TAK1 induces NF-kappa B activation through a novel NIK-independent signaling pathway.
包括核因子κB诱导激酶(NIK)在内的几种丝裂原活化蛋白激酶激酶激酶(MAPKKK)在核因子κB激活过程中发挥关键作用。我们分离出了人转化生长因子β激活激酶1(TAK1)的互补DNA(cDNA),TAK1是MAPKKK家族的一员,并评估了其刺激核因子κB激活的能力。TAK1与其激活蛋白TAK1结合蛋白1(TAB1)一起过表达,诱导了核因子κB p50/p65异二聚体的核转位,同时伴有IκBα和IκBβ的降解以及κB依赖性报告基因的表达。NIK的显性负性突变体并不抑制TAK1诱导的核因子κB激活。这些结果表明,TAK1通过一条不依赖NIK的新信号通路诱导核因子κB激活。