c-Myc Is a Nrf2-Interacting Protein that Negatively Regulates Phase II Genes Through Their Electrophile Responsive Elements

被引:54
作者
Levy, Smadar [1 ]
Forman, Henry Jay [1 ]
机构
[1] Univ Calif, Dept Nat Sci, Merced, CA USA
基金
美国国家卫生研究院;
关键词
c-Myc; Nrf2; EpRE; phase II genes; GAMMA-GLUTAMYLCYSTEINE SYNTHETASE; GLUTAMATE-CYSTEINE LIGASE; NAPHTHOFLAVONE-INDUCED EXPRESSION; ONCOGENIC TRANSCRIPTION FACTOR; HEAVY SUBUNIT GENE; NAD(P)H-QUINONE OXIDOREDUCTASE; ANTIOXIDANT DEFENSES; EPITHELIAL-CELLS; MELANOMA-CELLS; GLUTATHIONE;
D O I
10.1002/iub.314
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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) 2010 IUBMB IUBMB Life, 62(3): 237-246, 2010
引用
收藏
页码:237 / 246
页数:10
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