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Temporal competition between differentiation programs determines cell fate choice
Multipotent differentiation, where cells adopt one of several possible fates, occurs in diverse systems ranging from bacteria to mammals. This decision-making process is driven by multiple differentiation programs that operate simultaneously in the cell. How these programs interact to govern cell fa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Molecular Biology Organization
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737729/ https://www.ncbi.nlm.nih.gov/pubmed/22146301 http://dx.doi.org/10.1038/msb.2011.88 |
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author | Kuchina, Anna Espinar, Lorena Çaǧatay, Tolga Balbin, Alejandro O Zhang, Fang Alvarado, Alma Garcia-Ojalvo, Jordi Süel, Gürol M |
author_facet | Kuchina, Anna Espinar, Lorena Çaǧatay, Tolga Balbin, Alejandro O Zhang, Fang Alvarado, Alma Garcia-Ojalvo, Jordi Süel, Gürol M |
author_sort | Kuchina, Anna |
collection | PubMed |
description | Multipotent differentiation, where cells adopt one of several possible fates, occurs in diverse systems ranging from bacteria to mammals. This decision-making process is driven by multiple differentiation programs that operate simultaneously in the cell. How these programs interact to govern cell fate choice is poorly understood. To investigate this issue, we simultaneously measured activities of the competing sporulation and competence programs in single Bacillus subtilis cells. This approach revealed that these competing differentiation programs progress independently without cross-regulation before the decision point. Cells seem to arrive at a fate choice through differences in the relative timing between the two programs. To test this proposed dynamic mechanism, we altered the relative timing by engineering artificial cross-regulation between the sporulation and competence circuits. Results suggest a simple model that does not require a checkpoint or intricate cross-regulation before cellular decision-making. Rather, cell fate choice appears to be the outcome of a ‘molecular race’ between differentiation programs that compete in time, providing a simple dynamic mechanism for decision-making. |
format | Online Article Text |
id | pubmed-3737729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | European Molecular Biology Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-37377292013-08-08 Temporal competition between differentiation programs determines cell fate choice Kuchina, Anna Espinar, Lorena Çaǧatay, Tolga Balbin, Alejandro O Zhang, Fang Alvarado, Alma Garcia-Ojalvo, Jordi Süel, Gürol M Mol Syst Biol Article Multipotent differentiation, where cells adopt one of several possible fates, occurs in diverse systems ranging from bacteria to mammals. This decision-making process is driven by multiple differentiation programs that operate simultaneously in the cell. How these programs interact to govern cell fate choice is poorly understood. To investigate this issue, we simultaneously measured activities of the competing sporulation and competence programs in single Bacillus subtilis cells. This approach revealed that these competing differentiation programs progress independently without cross-regulation before the decision point. Cells seem to arrive at a fate choice through differences in the relative timing between the two programs. To test this proposed dynamic mechanism, we altered the relative timing by engineering artificial cross-regulation between the sporulation and competence circuits. Results suggest a simple model that does not require a checkpoint or intricate cross-regulation before cellular decision-making. Rather, cell fate choice appears to be the outcome of a ‘molecular race’ between differentiation programs that compete in time, providing a simple dynamic mechanism for decision-making. European Molecular Biology Organization 2011-12-06 /pmc/articles/PMC3737729/ /pubmed/22146301 http://dx.doi.org/10.1038/msb.2011.88 Text en Copyright © 2011, EMBO and Macmillan Publishers Limited https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial Share Alike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission. |
spellingShingle | Article Kuchina, Anna Espinar, Lorena Çaǧatay, Tolga Balbin, Alejandro O Zhang, Fang Alvarado, Alma Garcia-Ojalvo, Jordi Süel, Gürol M Temporal competition between differentiation programs determines cell fate choice |
title | Temporal competition between differentiation programs determines cell fate choice |
title_full | Temporal competition between differentiation programs determines cell fate choice |
title_fullStr | Temporal competition between differentiation programs determines cell fate choice |
title_full_unstemmed | Temporal competition between differentiation programs determines cell fate choice |
title_short | Temporal competition between differentiation programs determines cell fate choice |
title_sort | temporal competition between differentiation programs determines cell fate choice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737729/ https://www.ncbi.nlm.nih.gov/pubmed/22146301 http://dx.doi.org/10.1038/msb.2011.88 |
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