Nakajima Yoshihiro, Ikeda Masaaki, Kimura Takuma, Honma Sato, Ohmiya Yoshihiro, Honma Ken-ichi
Cell Dynamics Research Group, Research Institute for Cell Engineering, National Institute of Advanced Industrial Science and Technology (AIST), Midorigaoka, Ikeda, Osaka 563-8577, Japan.
FEBS Lett. 2004 May 7;565(1-3):122-6. doi: 10.1016/j.febslet.2004.03.083.
Circadian rhythms are generated by an extremely complicated transcription-translation feedback loop. To precisely analyze the molecular mechanisms of the circadian clock, it is critical to monitor multiple gene expressions and/or interactions with their transcription factors simultaneously. We have developed a novel reporter assay system, the tricolor reporter in vitro assay system, which consists of green- and red-emitting Phrixothrix luciferases as dual reporters and blue-emitting Renilla luciferase as internal control. We have successfully employed this system in analyzing the effects of clock gene products on the enhancer elements of Per1 and Bmal1 promoters. The results indicate that the orphan nuclear receptor RORalpha regulates bidirectionally Bmal1 (positively) and Per1 (negatively) transcriptions simultaneously.
昼夜节律由一个极其复杂的转录-翻译反馈环产生。为了精确分析生物钟的分子机制,同时监测多个基因的表达和/或它们与转录因子的相互作用至关重要。我们开发了一种新型报告基因检测系统,即三色报告基因体外检测系统,它由发出绿色和红色荧光的多管发光虫荧光素酶作为双报告基因,以及发出蓝色荧光的海肾荧光素酶作为内参组成。我们已成功应用该系统分析生物钟基因产物对Per1和Bmal1启动子增强子元件的影响。结果表明,孤儿核受体RORα同时双向调节Bmal1(正向)和Per1(负向)的转录。