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microRNA input into a neural ultradian oscillator controls emergence and timing of alternative cell states
Progenitor maintenance, timed differentiation and the potential to enter quiescence are three fundamental processes that underlie the development of any organ system. In the nervous system, progenitor cells show short-period oscillations in the expression of the transcriptional repressor Hes1, while...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3959193/ https://www.ncbi.nlm.nih.gov/pubmed/24595054 http://dx.doi.org/10.1038/ncomms4399 |
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author | Goodfellow, Marc Phillips, Nicholas E. Manning, Cerys Galla, Tobias Papalopulu, Nancy |
author_facet | Goodfellow, Marc Phillips, Nicholas E. Manning, Cerys Galla, Tobias Papalopulu, Nancy |
author_sort | Goodfellow, Marc |
collection | PubMed |
description | Progenitor maintenance, timed differentiation and the potential to enter quiescence are three fundamental processes that underlie the development of any organ system. In the nervous system, progenitor cells show short-period oscillations in the expression of the transcriptional repressor Hes1, while neurons and quiescent progenitors show stable low and high levels of Hes1, respectively. Here we use experimental data to develop a mathematical model of the double-negative interaction between Hes1 and a microRNA, miR-9, with the aim of understanding how cells transition from one state to another. We show that the input of miR-9 into the Hes1 oscillator tunes its oscillatory dynamics, and endows the system with bistability and the ability to measure time to differentiation. Our results suggest that a relatively simple and widespread network of cross-repressive interactions provides a unifying framework for progenitor maintenance, the timing of differentiation and the emergence of alternative cell states. |
format | Online Article Text |
id | pubmed-3959193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-39591932014-03-20 microRNA input into a neural ultradian oscillator controls emergence and timing of alternative cell states Goodfellow, Marc Phillips, Nicholas E. Manning, Cerys Galla, Tobias Papalopulu, Nancy Nat Commun Article Progenitor maintenance, timed differentiation and the potential to enter quiescence are three fundamental processes that underlie the development of any organ system. In the nervous system, progenitor cells show short-period oscillations in the expression of the transcriptional repressor Hes1, while neurons and quiescent progenitors show stable low and high levels of Hes1, respectively. Here we use experimental data to develop a mathematical model of the double-negative interaction between Hes1 and a microRNA, miR-9, with the aim of understanding how cells transition from one state to another. We show that the input of miR-9 into the Hes1 oscillator tunes its oscillatory dynamics, and endows the system with bistability and the ability to measure time to differentiation. Our results suggest that a relatively simple and widespread network of cross-repressive interactions provides a unifying framework for progenitor maintenance, the timing of differentiation and the emergence of alternative cell states. Nature Pub. Group 2014-03-04 /pmc/articles/PMC3959193/ /pubmed/24595054 http://dx.doi.org/10.1038/ncomms4399 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Article Goodfellow, Marc Phillips, Nicholas E. Manning, Cerys Galla, Tobias Papalopulu, Nancy microRNA input into a neural ultradian oscillator controls emergence and timing of alternative cell states |
title | microRNA input into a neural ultradian oscillator controls emergence and timing of alternative cell states |
title_full | microRNA input into a neural ultradian oscillator controls emergence and timing of alternative cell states |
title_fullStr | microRNA input into a neural ultradian oscillator controls emergence and timing of alternative cell states |
title_full_unstemmed | microRNA input into a neural ultradian oscillator controls emergence and timing of alternative cell states |
title_short | microRNA input into a neural ultradian oscillator controls emergence and timing of alternative cell states |
title_sort | microrna input into a neural ultradian oscillator controls emergence and timing of alternative cell states |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3959193/ https://www.ncbi.nlm.nih.gov/pubmed/24595054 http://dx.doi.org/10.1038/ncomms4399 |
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