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A direct repeat of E-box-like elements is required for cell-autonomous circadian rhythm of clock genes
BACKGROUND: The circadian expression of the mammalian clock genes is based on transcriptional feedback loops. Two basic helix-loop-helix (bHLH) PAS (for Period-Arnt-Sim) domain-containing transcriptional activators, CLOCK and BMAL1, are known to regulate gene expression by interacting with a promote...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2254435/ https://www.ncbi.nlm.nih.gov/pubmed/18177499 http://dx.doi.org/10.1186/1471-2199-9-1 |
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author | Nakahata, Yasukazu Yoshida, Mayumi Takano, Atsuko Soma, Haruhiko Yamamoto, Takuro Yasuda, Akio Nakatsu, Toru Takumi, Toru |
author_facet | Nakahata, Yasukazu Yoshida, Mayumi Takano, Atsuko Soma, Haruhiko Yamamoto, Takuro Yasuda, Akio Nakatsu, Toru Takumi, Toru |
author_sort | Nakahata, Yasukazu |
collection | PubMed |
description | BACKGROUND: The circadian expression of the mammalian clock genes is based on transcriptional feedback loops. Two basic helix-loop-helix (bHLH) PAS (for Period-Arnt-Sim) domain-containing transcriptional activators, CLOCK and BMAL1, are known to regulate gene expression by interacting with a promoter element termed the E-box (CACGTG). The non-canonical E-boxes or E-box-like sequences have also been reported to be necessary for circadian oscillation. RESULTS: We report a new cis-element required for cell-autonomous circadian transcription of clock genes. This new element consists of a canonical E-box or a non-canonical E-box and an E-box-like sequence in tandem with the latter with a short interval, 6 base pairs, between them. We demonstrate that both E-box or E-box-like sequences are needed to generate cell-autonomous oscillation. We also verify that the spacing nucleotides with constant length between these 2 E-elements are crucial for robust oscillation. Furthermore, by in silico analysis we conclude that several clock and clock-controlled genes possess a direct repeat of the E-box-like elements in their promoter region. CONCLUSION: We propose a novel possible mechanism regulated by double E-box-like elements, not to a single E-box, for circadian transcriptional oscillation. The direct repeat of the E-box-like elements identified in this study is the minimal required element for the generation of cell-autonomous transcriptional oscillation of clock and clock-controlled genes. |
format | Text |
id | pubmed-2254435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22544352008-02-26 A direct repeat of E-box-like elements is required for cell-autonomous circadian rhythm of clock genes Nakahata, Yasukazu Yoshida, Mayumi Takano, Atsuko Soma, Haruhiko Yamamoto, Takuro Yasuda, Akio Nakatsu, Toru Takumi, Toru BMC Mol Biol Research Article BACKGROUND: The circadian expression of the mammalian clock genes is based on transcriptional feedback loops. Two basic helix-loop-helix (bHLH) PAS (for Period-Arnt-Sim) domain-containing transcriptional activators, CLOCK and BMAL1, are known to regulate gene expression by interacting with a promoter element termed the E-box (CACGTG). The non-canonical E-boxes or E-box-like sequences have also been reported to be necessary for circadian oscillation. RESULTS: We report a new cis-element required for cell-autonomous circadian transcription of clock genes. This new element consists of a canonical E-box or a non-canonical E-box and an E-box-like sequence in tandem with the latter with a short interval, 6 base pairs, between them. We demonstrate that both E-box or E-box-like sequences are needed to generate cell-autonomous oscillation. We also verify that the spacing nucleotides with constant length between these 2 E-elements are crucial for robust oscillation. Furthermore, by in silico analysis we conclude that several clock and clock-controlled genes possess a direct repeat of the E-box-like elements in their promoter region. CONCLUSION: We propose a novel possible mechanism regulated by double E-box-like elements, not to a single E-box, for circadian transcriptional oscillation. The direct repeat of the E-box-like elements identified in this study is the minimal required element for the generation of cell-autonomous transcriptional oscillation of clock and clock-controlled genes. BioMed Central 2008-01-04 /pmc/articles/PMC2254435/ /pubmed/18177499 http://dx.doi.org/10.1186/1471-2199-9-1 Text en Copyright © 2008 Nakahata et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Nakahata, Yasukazu Yoshida, Mayumi Takano, Atsuko Soma, Haruhiko Yamamoto, Takuro Yasuda, Akio Nakatsu, Toru Takumi, Toru A direct repeat of E-box-like elements is required for cell-autonomous circadian rhythm of clock genes |
title | A direct repeat of E-box-like elements is required for cell-autonomous circadian rhythm of clock genes |
title_full | A direct repeat of E-box-like elements is required for cell-autonomous circadian rhythm of clock genes |
title_fullStr | A direct repeat of E-box-like elements is required for cell-autonomous circadian rhythm of clock genes |
title_full_unstemmed | A direct repeat of E-box-like elements is required for cell-autonomous circadian rhythm of clock genes |
title_short | A direct repeat of E-box-like elements is required for cell-autonomous circadian rhythm of clock genes |
title_sort | direct repeat of e-box-like elements is required for cell-autonomous circadian rhythm of clock genes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2254435/ https://www.ncbi.nlm.nih.gov/pubmed/18177499 http://dx.doi.org/10.1186/1471-2199-9-1 |
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