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Cell fate potentials and switching kinetics uncovered in a classic bistable genetic switch
Bistable switches are common gene regulatory motifs directing two mutually exclusive cell fates. Theoretical studies suggest that bistable switches are sufficient to encode more than two cell fates without rewiring the circuitry due to the non-equilibrium, heterogeneous cellular environment. However...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050291/ https://www.ncbi.nlm.nih.gov/pubmed/30018349 http://dx.doi.org/10.1038/s41467-018-05071-1 |
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author | Fang, Xiaona Liu, Qiong Bohrer, Christopher Hensel, Zach Han, Wei Wang, Jin Xiao, Jie |
author_facet | Fang, Xiaona Liu, Qiong Bohrer, Christopher Hensel, Zach Han, Wei Wang, Jin Xiao, Jie |
author_sort | Fang, Xiaona |
collection | PubMed |
description | Bistable switches are common gene regulatory motifs directing two mutually exclusive cell fates. Theoretical studies suggest that bistable switches are sufficient to encode more than two cell fates without rewiring the circuitry due to the non-equilibrium, heterogeneous cellular environment. However, such a scenario has not been experimentally observed. Here by developing a new, dual single-molecule gene-expression reporting system, we find that for the two mutually repressing transcription factors CI and Cro in the classic bistable bacteriophage λ switch, there exist two new production states, in which neither CI nor Cro is produced, or both CI and Cro are produced. We construct the corresponding potential landscape and map the transition kinetics among the four production states. These findings uncover cell fate potentials beyond the classical picture of bistable switches, and open a new window to explore the genetic and environmental origins of the cell fate decision-making process in gene regulatory networks. |
format | Online Article Text |
id | pubmed-6050291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60502912018-07-23 Cell fate potentials and switching kinetics uncovered in a classic bistable genetic switch Fang, Xiaona Liu, Qiong Bohrer, Christopher Hensel, Zach Han, Wei Wang, Jin Xiao, Jie Nat Commun Article Bistable switches are common gene regulatory motifs directing two mutually exclusive cell fates. Theoretical studies suggest that bistable switches are sufficient to encode more than two cell fates without rewiring the circuitry due to the non-equilibrium, heterogeneous cellular environment. However, such a scenario has not been experimentally observed. Here by developing a new, dual single-molecule gene-expression reporting system, we find that for the two mutually repressing transcription factors CI and Cro in the classic bistable bacteriophage λ switch, there exist two new production states, in which neither CI nor Cro is produced, or both CI and Cro are produced. We construct the corresponding potential landscape and map the transition kinetics among the four production states. These findings uncover cell fate potentials beyond the classical picture of bistable switches, and open a new window to explore the genetic and environmental origins of the cell fate decision-making process in gene regulatory networks. Nature Publishing Group UK 2018-07-17 /pmc/articles/PMC6050291/ /pubmed/30018349 http://dx.doi.org/10.1038/s41467-018-05071-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Fang, Xiaona Liu, Qiong Bohrer, Christopher Hensel, Zach Han, Wei Wang, Jin Xiao, Jie Cell fate potentials and switching kinetics uncovered in a classic bistable genetic switch |
title | Cell fate potentials and switching kinetics uncovered in a classic bistable genetic switch |
title_full | Cell fate potentials and switching kinetics uncovered in a classic bistable genetic switch |
title_fullStr | Cell fate potentials and switching kinetics uncovered in a classic bistable genetic switch |
title_full_unstemmed | Cell fate potentials and switching kinetics uncovered in a classic bistable genetic switch |
title_short | Cell fate potentials and switching kinetics uncovered in a classic bistable genetic switch |
title_sort | cell fate potentials and switching kinetics uncovered in a classic bistable genetic switch |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050291/ https://www.ncbi.nlm.nih.gov/pubmed/30018349 http://dx.doi.org/10.1038/s41467-018-05071-1 |
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