Noguchi K, Kokubu A, Kitanaka C, Ichijo H, Kuchino Y
Department of Bioactive Molecules, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo, 162-8640, Japan.
Biochem Biophys Res Commun. 2001 Mar;281(5):1313-20. doi: 10.1006/bbrc.2001.4498.
We previously reported that JNK is involved in the regulation of c-Myc-mediated apoptosis triggered by UV irradiation and anticancer drug treatment. Here we show that ASK1 is an upstream regulator for c-Myc-mediated apoptosis triggered by UV, and we found a direct role for Ser-62 and Ser-71 in the regulation of protein stability and function of c-Myc. The ASK1-JNK pathway enhanced the protein stability of c-Myc through phosphorylation at Ser-62 and Ser-71, which was required for c-Myc-dependent apoptosis by ASK1-signaling. Interestingly, ASK1-signaling attenuated the degradation of ubiquitinated c-Myc without affecting the ubiquitination process. Together, these findings indicate that the ASK1-JNK pathway promotes the proapoptotic activity of c-Myc by modulating c-Myc protein stability through phosphorylation at Ser-62 and Ser-71.
我们之前报道过,JNK参与紫外线照射和抗癌药物治疗引发的c-Myc介导的细胞凋亡的调控。在此我们表明,ASK1是紫外线引发的c-Myc介导的细胞凋亡的上游调节因子,并且我们发现Ser-62和Ser-71在c-Myc的蛋白质稳定性和功能调控中具有直接作用。ASK1-JNK通路通过Ser-62和Ser-71的磷酸化增强了c-Myc的蛋白质稳定性,这是ASK1信号传导导致的c-Myc依赖性细胞凋亡所必需的。有趣的是,ASK1信号传导减弱了泛素化c-Myc的降解,而不影响泛素化过程。总之,这些发现表明,ASK1-JNK通路通过在Ser-62和Ser-71处进行磷酸化来调节c-Myc蛋白质稳定性,从而促进c-Myc的促凋亡活性。