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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-7870843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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