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Number of active transcription factor binding sites is essential for the Hes7 oscillator

BACKGROUND: It is commonly accepted that embryonic segmentation of vertebrates is regulated by a segmentation clock, which is induced by the cycling genes Hes1 and Hes7. Their products form dimers that bind to the regulatory regions and thereby repress the transcription of their own encoding genes....

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Autores principales: Zeiser, Stefan, Liebscher, H Volkmar, Tiedemann, Hendrik, Rubio-Aliaga, Isabel, Przemeck, Gerhard KH, de Angelis, Martin Hrabé, Winkler, Gerhard
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1402261/
https://www.ncbi.nlm.nih.gov/pubmed/16504083
http://dx.doi.org/10.1186/1742-4682-3-11
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author Zeiser, Stefan
Liebscher, H Volkmar
Tiedemann, Hendrik
Rubio-Aliaga, Isabel
Przemeck, Gerhard KH
de Angelis, Martin Hrabé
Winkler, Gerhard
author_facet Zeiser, Stefan
Liebscher, H Volkmar
Tiedemann, Hendrik
Rubio-Aliaga, Isabel
Przemeck, Gerhard KH
de Angelis, Martin Hrabé
Winkler, Gerhard
author_sort Zeiser, Stefan
collection PubMed
description BACKGROUND: It is commonly accepted that embryonic segmentation of vertebrates is regulated by a segmentation clock, which is induced by the cycling genes Hes1 and Hes7. Their products form dimers that bind to the regulatory regions and thereby repress the transcription of their own encoding genes. An increase of the half-life of Hes7 protein causes irregular somite formation. This was shown in recent experiments by Hirata et al. In the same work, numerical simulations from a delay differential equations model, originally invented by Lewis, gave additional support. For a longer half-life of the Hes7 protein, these simulations exhibited strongly damped oscillations with, after few periods, severely attenuated the amplitudes. In these simulations, the Hill coefficient, a crucial model parameter, was set to 2 indicating that Hes7 has only one binding site in its promoter. On the other hand, Bessho et al. established three regulatory elements in the promoter region. RESULTS: We show that – with the same half life – the delay system is highly sensitive to changes in the Hill coefficient. A small increase changes the qualitative behaviour of the solutions drastically. There is sustained oscillation and hence the model can no longer explain the disruption of the segmentation clock. On the other hand, the Hill coefficient is correlated with the number of active binding sites, and with the way in which dimers bind to them. In this paper, we adopt response functions in order to estimate Hill coefficients for a variable number of active binding sites. It turns out that three active transcription factor binding sites increase the Hill coefficient by at least 20% as compared to one single active site. CONCLUSION: Our findings lead to the following crucial dichotomy: either Hirata's model is correct for the Hes7 oscillator, in which case at most two binding sites are active in its promoter region; or at least three binding sites are active, in which case Hirata's delay system does not explain the experimental results. Recent experiments by Chen et al. seem to support the former hypothesis, but the discussion is still open.
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spelling pubmed-14022612006-03-16 Number of active transcription factor binding sites is essential for the Hes7 oscillator Zeiser, Stefan Liebscher, H Volkmar Tiedemann, Hendrik Rubio-Aliaga, Isabel Przemeck, Gerhard KH de Angelis, Martin Hrabé Winkler, Gerhard Theor Biol Med Model Research BACKGROUND: It is commonly accepted that embryonic segmentation of vertebrates is regulated by a segmentation clock, which is induced by the cycling genes Hes1 and Hes7. Their products form dimers that bind to the regulatory regions and thereby repress the transcription of their own encoding genes. An increase of the half-life of Hes7 protein causes irregular somite formation. This was shown in recent experiments by Hirata et al. In the same work, numerical simulations from a delay differential equations model, originally invented by Lewis, gave additional support. For a longer half-life of the Hes7 protein, these simulations exhibited strongly damped oscillations with, after few periods, severely attenuated the amplitudes. In these simulations, the Hill coefficient, a crucial model parameter, was set to 2 indicating that Hes7 has only one binding site in its promoter. On the other hand, Bessho et al. established three regulatory elements in the promoter region. RESULTS: We show that – with the same half life – the delay system is highly sensitive to changes in the Hill coefficient. A small increase changes the qualitative behaviour of the solutions drastically. There is sustained oscillation and hence the model can no longer explain the disruption of the segmentation clock. On the other hand, the Hill coefficient is correlated with the number of active binding sites, and with the way in which dimers bind to them. In this paper, we adopt response functions in order to estimate Hill coefficients for a variable number of active binding sites. It turns out that three active transcription factor binding sites increase the Hill coefficient by at least 20% as compared to one single active site. CONCLUSION: Our findings lead to the following crucial dichotomy: either Hirata's model is correct for the Hes7 oscillator, in which case at most two binding sites are active in its promoter region; or at least three binding sites are active, in which case Hirata's delay system does not explain the experimental results. Recent experiments by Chen et al. seem to support the former hypothesis, but the discussion is still open. BioMed Central 2006-02-23 /pmc/articles/PMC1402261/ /pubmed/16504083 http://dx.doi.org/10.1186/1742-4682-3-11 Text en Copyright © 2006 Zeiser 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
Zeiser, Stefan
Liebscher, H Volkmar
Tiedemann, Hendrik
Rubio-Aliaga, Isabel
Przemeck, Gerhard KH
de Angelis, Martin Hrabé
Winkler, Gerhard
Number of active transcription factor binding sites is essential for the Hes7 oscillator
title Number of active transcription factor binding sites is essential for the Hes7 oscillator
title_full Number of active transcription factor binding sites is essential for the Hes7 oscillator
title_fullStr Number of active transcription factor binding sites is essential for the Hes7 oscillator
title_full_unstemmed Number of active transcription factor binding sites is essential for the Hes7 oscillator
title_short Number of active transcription factor binding sites is essential for the Hes7 oscillator
title_sort number of active transcription factor binding sites is essential for the hes7 oscillator
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1402261/
https://www.ncbi.nlm.nih.gov/pubmed/16504083
http://dx.doi.org/10.1186/1742-4682-3-11
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