Lim Chunghun, Chung Brian Y, Pitman Jena L, McGill Jermaine J, Pradhan Suraj, Lee Jongbin, Keegan Kevin P, Choe Joonho, Allada Ravi
Department of Neurobiology and Physiology, Northwestern University, Evanston, Illinois 60208, USA.
Curr Biol. 2007 Jun 19;17(12):1082-9. doi: 10.1016/j.cub.2007.05.039. Epub 2007 Jun 7.
Gene transcription is a central timekeeping process in animal clocks. In Drosophila, the basic helix-loop helix (bHLH)-PAS transcription-factor heterodimer, CLOCK/CYCLE (CLK/CYC), transcriptionally activates the clock components period (per), timeless (tim), Par domain protein 1 (Pdp1), and vrille (vri), which feed back and regulate distinct features of CLK/CYC function. Microarray studies have identified numerous rhythmically expressed transcripts, some of which are potential direct CLK targets. Here we demonstrate a circadian function for one such target, a bHLH-Orange repressor, CG17100/CLOCKWORK ORANGE (CWO). cwo is rhythmically expressed, and levels are reduced in Clk mutants, suggesting that cwo is CLK activated in vivo. cwo mutants display reduced-amplitude molecular and behavioral rhythms with lengthened periods. Molecular analysis suggests that CWO acts, in part, by repressing CLK target genes. We propose that CWO acts as a transcriptional and behavioral rhythm amplifier.
基因转录是动物生物钟中的一个核心计时过程。在果蝇中,基本的螺旋-环-螺旋(bHLH)-PAS转录因子异二聚体,即生物钟蛋白/周期蛋白(CLK/CYC),转录激活生物钟组分周期蛋白(per)、无时间性蛋白(tim)、同源结构域蛋白1(Pdp1)和维里蛋白(vri),这些组分反馈并调节CLK/CYC功能的不同特征。微阵列研究已鉴定出许多有节律表达的转录本,其中一些是CLK潜在的直接靶标。在此,我们证明了其中一个这样的靶标,即bHLH-橙色阻遏物CG17100/发条橙(CWO)具有昼夜节律功能。cwo有节律地表达,且在Clk突变体中的水平降低,这表明cwo在体内是由CLK激活的。cwo突变体表现出分子和行为节律的振幅降低且周期延长。分子分析表明,CWO部分通过抑制CLK靶基因发挥作用。我们提出,CWO作为转录和行为节律放大器发挥作用。