Allada R, White N E, So W V, Hall J C, Rosbash M
NSF, Center for Biological Timing, and Department of Biology, Brandeis University, Waltham, Massachusetts 02254, USA.
Cell. 1998 May 29;93(5):791-804. doi: 10.1016/s0092-8674(00)81440-3.
We report the identification, characterization, and cloning of a novel Drosophila circadian rhythm gene, dClock. The mutant, initially called Jrk, manifests dominant effects: heterozygous flies have a period alteration and half are arrhythmic, while homozygous flies are uniformly arrhythmic. Furthermore, these flies express low levels of the two clock proteins, PERIOD (PER) and TIMELESS (TIM), due to low per and tim transcription. Mapping and cloning of the Jrk gene indicates that it encodes the Drosophila homolog of mouse Clock. The mutant phenotype results from a premature stop codon that eliminates much of the putative activation domain of this bHLH-PAS transcription factor, thus explaining the dominant features of Jrk. The remarkable sequence conservation strongly supports common clock components present in the common ancestor of Drosophila and mammals.
我们报告了一个新的果蝇昼夜节律基因dClock的鉴定、特征描述及克隆。该突变体最初被称为Jrk,表现出显性效应:杂合子果蝇有周期改变,且一半无节律,而纯合子果蝇均无节律。此外,由于per和tim转录水平低,这些果蝇中两种生物钟蛋白,周期蛋白(PER)和无时间蛋白(TIM)的表达水平也低。Jrk基因的定位和克隆表明它编码小鼠Clock的果蝇同源物。突变体表型是由一个提前的终止密码子导致的,该密码子消除了这种bHLH-PAS转录因子的大部分假定激活结构域,从而解释了Jrk的显性特征。显著的序列保守性有力地支持了果蝇和哺乳动物共同祖先中存在的共同生物钟成分。