Department of Natural Sciences, University of California, Merced, USA.
IUBMB Life. 2010 Mar;62(3):237-46. doi: 10.1002/iub.314.
c-Myc is a transcription factor that is implicated in many cellular processes including proliferation, apoptosis and cancers. Recently, c-Myc was shown to be involved in regulation of glutamate cysteine ligase through E-box sequences. This investigation examined whether c-Myc also regulates phase II genes through interaction with the electrophile response element (EpRE). Experiments were conducted in human bronchial epithelial cells using si-RNA to knock down c-Myc. RT-PCR and reporter assays were used to measure transcription and promoter activity. c-Myc downregulated transcription and promoter activity of phase II genes. Chromatin immunoprecipitation verified binding of c-Myc to EpRE while coimmunoprecipitation demonstrated interaction of c-Myc with Nrf2. c-Myc also forms a ternary complex with Nrf2 and p-c-Jun. Finally, c-Myc decreased Nrf2 stability. Thus, our results suggest regulation of the EpRE/Nrf2 signaling pathway by c-Myc through both interaction with the EpRE binding complex and increased degradation of Nrf2.
c-Myc 是一种转录因子,涉及许多细胞过程,包括增殖、凋亡和癌症。最近,c-Myc 被证明通过 E 盒序列参与调节谷氨酸半胱氨酸连接酶。这项研究探讨了 c-Myc 是否通过与亲电物反应元件 (EpRE) 的相互作用来调节 II 相基因。在人支气管上皮细胞中进行了实验,使用 si-RNA 敲低 c-Myc。RT-PCR 和报告基因检测用于测量转录和启动子活性。c-Myc 下调 II 相基因的转录和启动子活性。染色质免疫沉淀验证了 c-Myc 与 EpRE 的结合,而共免疫沉淀证明了 c-Myc 与 Nrf2 的相互作用。c-Myc 还与 Nrf2 和 p-c-Jun 形成三元复合物。最后,c-Myc 降低了 Nrf2 的稳定性。因此,我们的结果表明 c-Myc 通过与 EpRE 结合复合物相互作用和增加 Nrf2 的降解来调节 EpRE/Nrf2 信号通路。