每1
生物钟
时钟
生物
振荡基因
细胞生物学
昼夜节律
电箱
遗传学
转录因子
抄写(语言学)
基因
增强子
神经科学
语言学
哲学
作者
Nicholas Gekakis,David Staknis,Hubert B. Nguyen,Fred C. Davis,Lisa D. Wilsbacher,David P. King,Joseph S. Takahashi,Charles J. Weitz
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1998-06-05
卷期号:280 (5369): 1564-1569
被引量:1976
标识
DOI:10.1126/science.280.5369.1564
摘要
The mouse Clock gene encodes a bHLH-PAS protein that regulates circadian rhythms and is related to transcription factors that act as heterodimers. Potential partners of CLOCK were isolated in a two-hybrid screen, and one, BMAL1, was coexpressed with CLOCK and PER1 at known circadian clock sites in brain and retina. CLOCK-BMAL1 heterodimers activated transcription from E-box elements, a type of transcription factor–binding site, found adjacent to the mouse per1 gene and from an identical E-box known to be important for per gene expression in Drosophila. Mutant CLOCK from the dominant-negative Clock allele and BMAL1 formed heterodimers that bound DNA but failed to activate transcription. Thus, CLOCK-BMAL1 heterodimers appear to drive the positive component of per transcriptional oscillations, which are thought to underlie circadian rhythmicity.
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