Vallone Daniela, Gondi Srinivas Babu, Whitmore David, Foulkes Nicholas S
Max-Planck-Institut für Entwicklungsbiologie, Spemannstrasse 35-39, D-72076 Tübingen, Germany.
Proc Natl Acad Sci U S A. 2004 Mar 23;101(12):4106-11. doi: 10.1073/pnas.0305436101. Epub 2004 Mar 15.
In most organisms, light plays a key role in the synchronization of the circadian timing system with the environmental day-night cycle. Light pulses that phase-shift the circadian clock also induce the expression of period (per) genes in vertebrates. Here, we report the cloning of a zebrafish per gene, zfper4, which is remarkable in being repressed by light. We have developed an in vivo luciferase reporter assay for this gene in cells that contain a light-entrainable clock. High-definition bioluminescence traces have enabled us to accurately measure phase-shifting of the clock by light. We have also exploited this model to study how four E-box elements in the zfper4 promoter regulate expression. Mutagenesis reveals that the integrity of these four E-boxes is crucial for maintaining low basal expression together with robust rhythmicity and repression by light. Importantly, in the context of a minimal heterologous promoter, the E-box elements also direct a robust circadian rhythm of expression that is significantly phase-advanced compared with the original zfper4 promoter and lacks the light-repression property. Thus, these results reveal flexibility in the phase and light responsiveness of E-box-directed rhythmic expression, depending on the promoter context.
在大多数生物体中,光在昼夜节律计时系统与环境昼夜循环的同步过程中起着关键作用。能使昼夜节律钟发生相位移动的光脉冲也会诱导脊椎动物中周期(per)基因的表达。在此,我们报告斑马鱼per基因zfper4的克隆,该基因的显著特点是受光抑制。我们针对这个基因在含有可光调节时钟的细胞中开发了一种体内荧光素酶报告基因检测方法。高清晰度生物发光轨迹使我们能够精确测量光对时钟的相位移动。我们还利用这个模型研究了zfper4启动子中的四个E盒元件如何调节表达。诱变结果表明,这四个E盒的完整性对于维持低基础表达、强大的节律性以及光抑制作用至关重要。重要的是,在最小异源启动子的背景下,E盒元件也能指导一种强大的昼夜节律表达,与原始的zfper4启动子相比,其相位显著提前,并且缺乏光抑制特性。因此,这些结果揭示了E盒指导的节律性表达在相位和光反应性方面的灵活性,这取决于启动子背景。