Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Goodfellow, Marc, Phillips, Nicholas E., Manning, Cerys, Galla, Tobias, Papalopulu, Nancy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2014
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
_version_ 1782308008429092864
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
work_keys_str_mv AT goodfellowmarc micrornainputintoaneuralultradianoscillatorcontrolsemergenceandtimingofalternativecellstates
AT phillipsnicholase micrornainputintoaneuralultradianoscillatorcontrolsemergenceandtimingofalternativecellstates
AT manningcerys micrornainputintoaneuralultradianoscillatorcontrolsemergenceandtimingofalternativecellstates
AT gallatobias micrornainputintoaneuralultradianoscillatorcontrolsemergenceandtimingofalternativecellstates
AT papalopulunancy micrornainputintoaneuralultradianoscillatorcontrolsemergenceandtimingofalternativecellstates