A mutant Drosophila homolog of mammalian Clock disrupts circadian rhythms and transcription of period and timeless

被引:614
作者
Allada, R
White, NE
So, WV
Hall, JC
Rosbash, M [1 ]
机构
[1] Brandeis Univ, Howard Hughes Med Inst, Waltham, MA 02254 USA
[2] Brandeis Univ, Ctr Biol Timing, NSF, Waltham, MA 02254 USA
[3] Brandeis Univ, Dept Biol, Waltham, MA 02254 USA
[4] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
D O I
10.1016/S0092-8674(00)81440-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:791 / 804
页数:14
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