Jin D Y, Teramoto H, Giam C Z, Chun R F, Gutkind J S, Jeang K T
Molecular Virology Section, Laboratory of Molecular Microbiology, NIAID, National Institutes of Health, Bethesda, Maryland 20892-0460, USA.
J Biol Chem. 1997 Oct 10;272(41):25816-23. doi: 10.1074/jbc.272.41.25816.
Tumor necrosis factor alpha (TNFalpha) has pleiotropic effects on cellular metabolism. One of the signaling paths from the TNFalpha receptor induces a stress-activated protein kinase cascade. Components within this TNFalpha kinase cascade include mitogen-activated protein kinase/extracellular signal-regulated kinase kinase kinase 1 (MEKK1) and stress-activated protein kinase/extracellular signal-regulated kinase kinase (SEK), which regulate the activity of c-Jun N-terminal kinase 1 (JNK1). Currently, molecules upstream of MEKK1 that link TNFalpha receptor to downstream kinases are not well understood. Besides TNFalpha, many other stimuli including several oncoproteins can activate JNK1. In most cases, the signaling cascade(s) leading from oncoproteins to JNK1 is poorly elucidated. We report here that the human T-cell lymphotrophic virus, type I (HTLV-I) oncoprotein, Tax, can activate JNK1. We isolated a novel human cell factor, G-protein pathway suppressor 2 (GPS2), by its ability to bind the HTLV-I oncoprotein, and we show that this factor can potently suppress Tax activation of JNK1. In trying to understand the mechanism of GPS2 activity, we found that it also suppressed TNFalpha activation of JNK1 but not TNFalpha activation of p38 kinase nor phorbol activation of extracellular signal-regulated kinase 2. Because GPS2 has minimal effect on MEKK1- or SEK-regulated JNK1 activity, it could act at a point between the TNFalpha receptor and MEKK1 in the initial step(s) of this kinase cascade. Alternatively, it is not excluded that GPS2 could work in a parallel pathway that leads from TNFalpha to JNK1. GPS2 represents a new molecule that could contribute important insights toward how cytokine- and oncoprotein-mediated signal transduction might converge.
肿瘤坏死因子α(TNFα)对细胞代谢具有多效性作用。TNFα受体的一条信号通路可诱导应激激活蛋白激酶级联反应。该TNFα激酶级联反应中的成分包括丝裂原活化蛋白激酶/细胞外信号调节激酶激酶激酶1(MEKK1)和应激激活蛋白激酶/细胞外信号调节激酶激酶(SEK),它们调节c-Jun氨基末端激酶1(JNK1)的活性。目前,将TNFα受体与下游激酶连接起来的MEKK1上游分子尚不清楚。除了TNFα,许多其他刺激因素,包括几种癌蛋白,都能激活JNK1。在大多数情况下,从癌蛋白到JNK1的信号级联反应尚不清楚。我们在此报告,人类I型嗜T细胞病毒(HTLV-I)癌蛋白Tax可激活JNK1。我们通过其与HTLV-I癌蛋白结合的能力分离出一种新型人类细胞因子,即G蛋白途径抑制因子2(GPS2),并且我们表明该因子可有效抑制Tax对JNK1的激活。在试图了解GPS2活性机制的过程中,我们发现它还抑制TNFα对JNK1的激活,但不抑制TNFα对p38激酶的激活,也不抑制佛波醇对细胞外信号调节激酶2的激活。由于GPS2对MEKK1或SEK调节的JNK1活性影响极小,它可能在该激酶级联反应的初始步骤中作用于TNFα受体和MEKK1之间的某个点。或者,不排除GPS2可以在从TNFα到JNK1的平行途径中发挥作用。GPS2代表一种新分子,它可能为细胞因子和癌蛋白介导的信号转导如何汇聚提供重要见解。