Cheung Po-Yan, Zhang Yi, Long Jiafu, Lin Shengcai, Zhang Mingjie, Jiang Yong, Wu Zhenguo
Department of Biochemistry, Hong Kong University of Science & Technology, Clear Water Bay, Kowloon, Hong Kong, China.
J Biol Chem. 2004 Oct 29;279(44):45308-11. doi: 10.1074/jbc.C400333200. Epub 2004 Sep 16.
To look for regulators of the mitogen-activated protein kinase (MAPK) kinase 6 (MKK6), a yeast two-hybrid screen was initiated using MKK6 as bait. p150(Glued) dynactin, a key component of the cytoplasmic dynein-dynactin motor complex, was found to specifically interact with MKK6 and its close homologue MKK3. Silencing of p150(Glued) expression by small interference RNA reduced the stimulus-induced phosphorylation of MKK3/6 and p38 MAPKs. The similar adverse effect was also seen when the cytoplasmic dynein motor was disrupted by other means. Like p150(Glued), MKK3/6 directly associate with microtubules. Disruption of microtubules prior to cell stimulation specifically inhibits the stimulus-induced phosphorylation of both MKK3/6 and p38 MAPKs. Our unexpected findings reveal a specific requirement for p150(Glued)/dynein/functional microtubules in activation of MKK3/6 and p38 MAPKs in vivo.
为寻找丝裂原活化蛋白激酶(MAPK)激酶6(MKK6)的调节因子,以MKK6为诱饵开展了酵母双杂交筛选。动力蛋白激活蛋白p150(Glued)是胞质动力蛋白-动力蛋白激活蛋白复合物的关键组分,被发现可与MKK6及其紧密同源物MKK3特异性相互作用。通过小干扰RNA沉默p150(Glued)的表达,可降低刺激诱导的MKK3/6和p38 MAPK的磷酸化水平。当通过其他方式破坏胞质动力蛋白时,也观察到了类似的不利影响。与p150(Glued)一样,MKK3/6也直接与微管相关。在细胞刺激前破坏微管,可特异性抑制刺激诱导的MKK3/6和p38 MAPK的磷酸化。我们意外的发现揭示了体内MKK3/6和p38 MAPK激活过程中对p150(Glued)/动力蛋白/功能性微管的特定需求。