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Winner-takes-all resource competition redirects cascading cell fate transitions

Failure of modularity remains a significant challenge for assembling synthetic gene circuits with tested modules as they often do not function as expected. Competition over shared limited gene expression resources is a crucial underlying reason. It was reported that resource competition makes two se...

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Autores principales: Zhang, Rong, Goetz, Hanah, Melendez-Alvarez, Juan, Li, Jiao, Ding, Tian, Wang, Xiao, Tian, Xiao-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870843/
https://www.ncbi.nlm.nih.gov/pubmed/33558556
http://dx.doi.org/10.1038/s41467-021-21125-3
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author Zhang, Rong
Goetz, Hanah
Melendez-Alvarez, Juan
Li, Jiao
Ding, Tian
Wang, Xiao
Tian, Xiao-Jun
author_facet Zhang, Rong
Goetz, Hanah
Melendez-Alvarez, Juan
Li, Jiao
Ding, Tian
Wang, Xiao
Tian, Xiao-Jun
author_sort Zhang, Rong
collection PubMed
description Failure of modularity remains a significant challenge for assembling synthetic gene circuits with tested modules as they often do not function as expected. Competition over shared limited gene expression resources is a crucial underlying reason. It was reported that resource competition makes two seemingly separate genes connect in a graded linear manner. Here we unveil nonlinear resource competition within synthetic gene circuits. We first build a synthetic cascading bistable switches (Syn-CBS) circuit in a single strain with two coupled self-activation modules to achieve two successive cell fate transitions. Interestingly, we find that the in vivo transition path was redirected as the activation of one switch always prevails against the other, contrary to the theoretically expected coactivation. This qualitatively different type of resource competition between the two modules follows a ‘winner-takes-all’ rule, where the winner is determined by the relative connection strength between the modules. To decouple the resource competition, we construct a two-strain circuit, which achieves successive activation and stable coactivation of the two switches. These results illustrate that a highly nonlinear hidden interaction between the circuit modules due to resource competition may cause counterintuitive consequences on circuit functions, which can be controlled with a division of labor strategy.
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spelling pubmed-78708432021-02-11 Winner-takes-all resource competition redirects cascading cell fate transitions Zhang, Rong Goetz, Hanah Melendez-Alvarez, Juan Li, Jiao Ding, Tian Wang, Xiao Tian, Xiao-Jun Nat Commun Article Failure of modularity remains a significant challenge for assembling synthetic gene circuits with tested modules as they often do not function as expected. Competition over shared limited gene expression resources is a crucial underlying reason. It was reported that resource competition makes two seemingly separate genes connect in a graded linear manner. Here we unveil nonlinear resource competition within synthetic gene circuits. We first build a synthetic cascading bistable switches (Syn-CBS) circuit in a single strain with two coupled self-activation modules to achieve two successive cell fate transitions. Interestingly, we find that the in vivo transition path was redirected as the activation of one switch always prevails against the other, contrary to the theoretically expected coactivation. This qualitatively different type of resource competition between the two modules follows a ‘winner-takes-all’ rule, where the winner is determined by the relative connection strength between the modules. To decouple the resource competition, we construct a two-strain circuit, which achieves successive activation and stable coactivation of the two switches. These results illustrate that a highly nonlinear hidden interaction between the circuit modules due to resource competition may cause counterintuitive consequences on circuit functions, which can be controlled with a division of labor strategy. Nature Publishing Group UK 2021-02-08 /pmc/articles/PMC7870843/ /pubmed/33558556 http://dx.doi.org/10.1038/s41467-021-21125-3 Text en © The Author(s) 2021 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
Zhang, Rong
Goetz, Hanah
Melendez-Alvarez, Juan
Li, Jiao
Ding, Tian
Wang, Xiao
Tian, Xiao-Jun
Winner-takes-all resource competition redirects cascading cell fate transitions
title Winner-takes-all resource competition redirects cascading cell fate transitions
title_full Winner-takes-all resource competition redirects cascading cell fate transitions
title_fullStr Winner-takes-all resource competition redirects cascading cell fate transitions
title_full_unstemmed Winner-takes-all resource competition redirects cascading cell fate transitions
title_short Winner-takes-all resource competition redirects cascading cell fate transitions
title_sort winner-takes-all resource competition redirects cascading cell fate transitions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870843/
https://www.ncbi.nlm.nih.gov/pubmed/33558556
http://dx.doi.org/10.1038/s41467-021-21125-3
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