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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...

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Autores principales: Fang, Xiaona, Liu, Qiong, Bohrer, Christopher, Hensel, Zach, Han, Wei, Wang, Jin, Xiao, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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