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Functional D-box sequences reset the circadian clock and drive mRNA rhythms
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 competit...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687812/ https://www.ncbi.nlm.nih.gov/pubmed/31428688 http://dx.doi.org/10.1038/s42003-019-0522-3 |
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author | Yoshitane, Hikari Asano, Yoshimasa Sagami, Aya Sakai, Seinosuke Suzuki, Yutaka Okamura, Hitoshi Iwasaki, Wataru Ozaki, Haruka Fukada, Yoshitaka |
author_facet | Yoshitane, Hikari Asano, Yoshimasa Sagami, Aya Sakai, Seinosuke Suzuki, Yutaka Okamura, Hitoshi Iwasaki, Wataru Ozaki, Haruka Fukada, Yoshitaka |
author_sort | Yoshitane, Hikari |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6687812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66878122019-08-19 Functional D-box sequences reset the circadian clock and drive mRNA rhythms Yoshitane, Hikari Asano, Yoshimasa Sagami, Aya Sakai, Seinosuke Suzuki, Yutaka Okamura, Hitoshi Iwasaki, Wataru Ozaki, Haruka Fukada, Yoshitaka Commun Biol Article 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. Nature Publishing Group UK 2019-08-08 /pmc/articles/PMC6687812/ /pubmed/31428688 http://dx.doi.org/10.1038/s42003-019-0522-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yoshitane, Hikari Asano, Yoshimasa Sagami, Aya Sakai, Seinosuke Suzuki, Yutaka Okamura, Hitoshi Iwasaki, Wataru Ozaki, Haruka Fukada, Yoshitaka Functional D-box sequences reset the circadian clock and drive mRNA rhythms |
title | Functional D-box sequences reset the circadian clock and drive mRNA rhythms |
title_full | Functional D-box sequences reset the circadian clock and drive mRNA rhythms |
title_fullStr | Functional D-box sequences reset the circadian clock and drive mRNA rhythms |
title_full_unstemmed | Functional D-box sequences reset the circadian clock and drive mRNA rhythms |
title_short | Functional D-box sequences reset the circadian clock and drive mRNA rhythms |
title_sort | functional d-box sequences reset the circadian clock and drive mrna rhythms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687812/ https://www.ncbi.nlm.nih.gov/pubmed/31428688 http://dx.doi.org/10.1038/s42003-019-0522-3 |
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