Functional D-box sequences reset the circadian clock and drive mRNA rhythms

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作者
Hikari Yoshitane
Yoshimasa Asano
Aya Sagami
Seinosuke Sakai
Yutaka Suzuki
Hitoshi Okamura
Wataru Iwasaki
Haruka Ozaki
Yoshitaka Fukada
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[1] The University of Tokyo,Department of Biological Sciences, School of Science
[2] The University of Tokyo,Department of Medical Genome Sciences, Graduate School of Frontier Sciences
[3] Kyoto University,Department of Systems Biology, Graduate School of Pharmaceutical Sciences
[4] University of Tsukuba,Bioinformatics Laboratory, Faculty of Medicine
[5] University of Tsukuba,Center for Artificial Intelligence Research
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The circadian clock drives gene expression rhythms, leading to daily changes in physiology and behavior. In mammals, Albumin D-site-Binding Protein (DBP) rhythmically activates transcription of various genes through a DNA cis-element, D-box. The DBP-dependent transactivation is repressed by competitive binding of E4BP4 to the D-box. Despite the elaborate regulation, physiological roles of the D-box in the circadian clockwork are still elusive. Here we identified 1490 genomic regions recognized commonly by DBP and E4BP4 in the mouse liver. We comprehensively defined functional D-box sequences using an improved bioinformatics method, MOCCS2. In RNA-Seq analysis of E4bp4-knockout and wild type liver, we showed the importance of E4BP4-mediated circadian repression in gene expression rhythms. In addition to the circadian control, we found that environmental stimuli caused acute induction of E4BP4 protein, evoking phase-dependent phase shifts of cellular circadian rhythms and resetting the clock. Collectively, D-box-mediated transcriptional regulation plays pivotal roles in input and output in the circadian clock system.
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