Closing the circadian loop:: CLOCK-induced transcription of its own inhibitors per and tim

被引:690
作者
Darlington, TK
Wager-Smith, K
Ceriani, MF
Staknis, D
Gekakis, N
Steeves, TDL
Weitz, CJ
Takahashi, JS
Kay, SA
机构
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92093 USA
[2] Scripps Res Inst, NSF, Ctr Biol Timing, La Jolla, CA 92093 USA
[3] Harvard Univ, Sch Med, Dept Neurobiol, Boston, MA 02115 USA
[4] Northwestern Univ, NSF,Ctr Biol Timing, Howard Hughes Med Inst, Dept Neurobiol & Physiol, Evanston, IL 60208 USA
关键词
D O I
10.1126/science.280.5369.1599
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The circadian oscillator generates a rhythmic output with a period of about 24 hours. Despite extensive studies in several model systems, the biochemical mode of action has not yet been demonstrated for any of its components. Here, the Drosophila CLOCK protein was shown to induce transcription of the circadian rhythm genes period and timeless. dCLOCK functioned as a heterodimer with a Drosophila homolog of BMAL1. These proteins acted through an E-box sequence in the period promoter. The timeless promoter contains an 18-base pair element encompassing an E-box, which was sufficient to confer dCLOCK responsiveness to a reporter gene. PERIOD and TIMELESS proteins blocked dCLOCK's ability to transactivate their promoters via the E-box. Thus, dCLOCK drives expression of period and timeless, which in turn inhibit dCLOCK's activity and close the circadian loop.
引用
收藏
页码:1599 / 1603
页数:5
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