Abstract
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.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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ARNTL Transcription Factors
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Animals
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Basic Helix-Loop-Helix Transcription Factors
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Biological Clocks
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CLOCK Proteins
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Cell Cycle Proteins
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Circadian Rhythm / genetics
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Circadian Rhythm / physiology*
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Cloning, Molecular
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Cricetinae
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DNA / metabolism
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Dimerization
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Feedback
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Gene Expression
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Helix-Loop-Helix Motifs
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Male
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Mesocricetus
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Mice
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Mutation
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Nuclear Proteins / genetics*
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Nuclear Proteins / metabolism
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Period Circadian Proteins
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Promoter Regions, Genetic
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Retina / metabolism
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Suprachiasmatic Nucleus / metabolism
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Trans-Activators / genetics
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Trans-Activators / metabolism*
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Transcription Factors / genetics
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Transcription Factors / metabolism*
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Transcriptional Activation*
Substances
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ARNTL Transcription Factors
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Arntl protein, mouse
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Basic Helix-Loop-Helix Transcription Factors
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Cell Cycle Proteins
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Nuclear Proteins
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Per1 protein, mouse
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Period Circadian Proteins
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Trans-Activators
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Transcription Factors
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DNA
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CLOCK Proteins
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Clock protein, mouse