Saez L, Meyer P, Young M W
Laboratory of Genetics, The Rockefeller University, New York, New York 10021, USA.
Cold Spring Harb Symp Quant Biol. 2007;72:69-74. doi: 10.1101/sqb.2007.72.034.
Circadian rhythms in Drosophila are supported by a negative feedback loop, in which PERIOD (PER) and Timeless (TIM) shut down their own transcription as they translocate once a day from the cytoplasm of clock-containing cells to the nucleus. Period length is partially determined by an interval of cytoplasmic retention of the TIM and PER proteins. To study this process, we examined PER/TIM/Doubletime (DBT) physical interactions and nuclear translocation by imaging individual cultured Drosophila cells. Using live cell video microscopy and green fluorescent protein (GFP) tags, we observed dynamic patterns of stability and localization for DBT, PER, and TIM that resembled those previously found in vivo. These studies suggest that a cytoplasmic interval timer regulates nuclear translocation of these proteins. The cultured cell assay provides a potent system to study interactions among new and known genes involved in the generation of circadian behavior.
果蝇的昼夜节律由一个负反馈回路维持,在这个回路中,周期蛋白(PER)和无时间蛋白(TIM)每天从含时钟细胞的细胞质转移到细胞核一次,在此过程中它们会关闭自身的转录。周期长度部分由TIM和PER蛋白在细胞质中的保留时间间隔决定。为了研究这个过程,我们通过对单个培养的果蝇细胞进行成像,检测了PER/TIM/双时相蛋白(DBT)的物理相互作用和核转运。利用活细胞视频显微镜和绿色荧光蛋白(GFP)标签,我们观察到DBT、PER和TIM的稳定性和定位动态模式,这些模式与之前在体内发现的相似。这些研究表明,细胞质间隔定时器调节这些蛋白质的核转运。培养细胞检测为研究参与昼夜节律行为产生的新基因和已知基因之间的相互作用提供了一个有力的系统。