Cargando…
Potential contribution of tandem circadian enhancers to nonlinear oscillations in clock gene expression
Limit-cycle oscillations require the presence of nonlinear processes. Although mathematical studies have long suggested that multiple nonlinear processes are required for autonomous circadian oscillation in clock gene expression, the underlying mechanism remains controversial. Here we show experimen...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555660/ https://www.ncbi.nlm.nih.gov/pubmed/28637769 http://dx.doi.org/10.1091/mbc.E17-02-0129 |
_version_ | 1783256953053511680 |
---|---|
author | Tokuda, Isao T. Okamoto, Akihiko Matsumura, Ritsuko Takumi, Toru Akashi, Makoto |
author_facet | Tokuda, Isao T. Okamoto, Akihiko Matsumura, Ritsuko Takumi, Toru Akashi, Makoto |
author_sort | Tokuda, Isao T. |
collection | PubMed |
description | Limit-cycle oscillations require the presence of nonlinear processes. Although mathematical studies have long suggested that multiple nonlinear processes are required for autonomous circadian oscillation in clock gene expression, the underlying mechanism remains controversial. Here we show experimentally that cell-autonomous circadian transcription of a mammalian clock gene requires a functionally interdependent tandem E-box motif; the lack of either of the two E-boxes results in arrhythmic transcription. Although previous studies indicated the role of the tandem motifs in increasing circadian amplitude, enhancing amplitude does not explain the mechanism for limit-cycle oscillations in transcription. In this study, mathematical analysis suggests that the interdependent behavior of enhancer elements including not only E-boxes but also ROR response elements might contribute to limit-cycle oscillations by increasing transcriptional nonlinearity. As expected, introduction of the interdependence of circadian enhancer elements into mathematical models resulted in autonomous transcriptional oscillation with low Hill coefficients. Together these findings suggest that interdependent tandem enhancer motifs on multiple clock genes might cooperatively enhance nonlinearity in the whole circadian feedback system, which would lead to limit-cycle oscillations in clock gene expression. |
format | Online Article Text |
id | pubmed-5555660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-55556602017-10-30 Potential contribution of tandem circadian enhancers to nonlinear oscillations in clock gene expression Tokuda, Isao T. Okamoto, Akihiko Matsumura, Ritsuko Takumi, Toru Akashi, Makoto Mol Biol Cell Articles Limit-cycle oscillations require the presence of nonlinear processes. Although mathematical studies have long suggested that multiple nonlinear processes are required for autonomous circadian oscillation in clock gene expression, the underlying mechanism remains controversial. Here we show experimentally that cell-autonomous circadian transcription of a mammalian clock gene requires a functionally interdependent tandem E-box motif; the lack of either of the two E-boxes results in arrhythmic transcription. Although previous studies indicated the role of the tandem motifs in increasing circadian amplitude, enhancing amplitude does not explain the mechanism for limit-cycle oscillations in transcription. In this study, mathematical analysis suggests that the interdependent behavior of enhancer elements including not only E-boxes but also ROR response elements might contribute to limit-cycle oscillations by increasing transcriptional nonlinearity. As expected, introduction of the interdependence of circadian enhancer elements into mathematical models resulted in autonomous transcriptional oscillation with low Hill coefficients. Together these findings suggest that interdependent tandem enhancer motifs on multiple clock genes might cooperatively enhance nonlinearity in the whole circadian feedback system, which would lead to limit-cycle oscillations in clock gene expression. The American Society for Cell Biology 2017-08-15 /pmc/articles/PMC5555660/ /pubmed/28637769 http://dx.doi.org/10.1091/mbc.E17-02-0129 Text en © 2017 Tokuda, Okamoto, et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. |
spellingShingle | Articles Tokuda, Isao T. Okamoto, Akihiko Matsumura, Ritsuko Takumi, Toru Akashi, Makoto Potential contribution of tandem circadian enhancers to nonlinear oscillations in clock gene expression |
title | Potential contribution of tandem circadian enhancers to nonlinear oscillations in clock gene expression |
title_full | Potential contribution of tandem circadian enhancers to nonlinear oscillations in clock gene expression |
title_fullStr | Potential contribution of tandem circadian enhancers to nonlinear oscillations in clock gene expression |
title_full_unstemmed | Potential contribution of tandem circadian enhancers to nonlinear oscillations in clock gene expression |
title_short | Potential contribution of tandem circadian enhancers to nonlinear oscillations in clock gene expression |
title_sort | potential contribution of tandem circadian enhancers to nonlinear oscillations in clock gene expression |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555660/ https://www.ncbi.nlm.nih.gov/pubmed/28637769 http://dx.doi.org/10.1091/mbc.E17-02-0129 |
work_keys_str_mv | AT tokudaisaot potentialcontributionoftandemcircadianenhancerstononlinearoscillationsinclockgeneexpression AT okamotoakihiko potentialcontributionoftandemcircadianenhancerstononlinearoscillationsinclockgeneexpression AT matsumuraritsuko potentialcontributionoftandemcircadianenhancerstononlinearoscillationsinclockgeneexpression AT takumitoru potentialcontributionoftandemcircadianenhancerstononlinearoscillationsinclockgeneexpression AT akashimakoto potentialcontributionoftandemcircadianenhancerstononlinearoscillationsinclockgeneexpression |