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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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Nicholas Gekakis
Carnegie Mellon University
David Staknis
Harvard University
Hubert B. Nguyen
Northeastern University
Science
Harvard University
Howard Hughes Medical Institute
Northeastern University
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Gekakis et al. (Fri,) studied this question.
synapsesocial.com/papers/6a00c79bda5c1eb07f2dbadc — DOI: https://doi.org/10.1126/science.280.5369.1564
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