Cargando…
A continuous-time stochastic Boolean model provides a quantitative description of the budding yeast cell cycle
The cell division cycle is regulated by a complex network of interacting genes and proteins. The control system has been modeled in many ways, from qualitative Boolean switching-networks to quantitative differential equations and highly detailed stochastic simulations. Here we develop a continuous-t...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700812/ https://www.ncbi.nlm.nih.gov/pubmed/36434030 http://dx.doi.org/10.1038/s41598-022-24302-6 |
_version_ | 1784839394417442816 |
---|---|
author | Laomettachit, Teeraphan Kraikivski, Pavel Tyson, John J. |
author_facet | Laomettachit, Teeraphan Kraikivski, Pavel Tyson, John J. |
author_sort | Laomettachit, Teeraphan |
collection | PubMed |
description | The cell division cycle is regulated by a complex network of interacting genes and proteins. The control system has been modeled in many ways, from qualitative Boolean switching-networks to quantitative differential equations and highly detailed stochastic simulations. Here we develop a continuous-time stochastic model using seven Boolean variables to represent the activities of major regulators of the budding yeast cell cycle plus one continuous variable representing cell growth. The Boolean variables are updated asynchronously by logical rules based on known biochemistry of the cell-cycle control system using Gillespie’s stochastic simulation algorithm. Time and cell size are updated continuously. By simulating a population of yeast cells, we calculate statistical properties of cell cycle progression that can be compared directly to experimental measurements. Perturbations of the normal sequence of events indicate that the cell cycle is 91% robust to random ‘flips’ of the Boolean variables, but 9% of the perturbations induce lethal mistakes in cell cycle progression. This simple, hybrid Boolean model gives a good account of the growth and division of budding yeast cells, suggesting that this modeling approach may be as accurate as detailed reaction-kinetic modeling with considerably less demands on estimating rate constants. |
format | Online Article Text |
id | pubmed-9700812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97008122022-11-27 A continuous-time stochastic Boolean model provides a quantitative description of the budding yeast cell cycle Laomettachit, Teeraphan Kraikivski, Pavel Tyson, John J. Sci Rep Article The cell division cycle is regulated by a complex network of interacting genes and proteins. The control system has been modeled in many ways, from qualitative Boolean switching-networks to quantitative differential equations and highly detailed stochastic simulations. Here we develop a continuous-time stochastic model using seven Boolean variables to represent the activities of major regulators of the budding yeast cell cycle plus one continuous variable representing cell growth. The Boolean variables are updated asynchronously by logical rules based on known biochemistry of the cell-cycle control system using Gillespie’s stochastic simulation algorithm. Time and cell size are updated continuously. By simulating a population of yeast cells, we calculate statistical properties of cell cycle progression that can be compared directly to experimental measurements. Perturbations of the normal sequence of events indicate that the cell cycle is 91% robust to random ‘flips’ of the Boolean variables, but 9% of the perturbations induce lethal mistakes in cell cycle progression. This simple, hybrid Boolean model gives a good account of the growth and division of budding yeast cells, suggesting that this modeling approach may be as accurate as detailed reaction-kinetic modeling with considerably less demands on estimating rate constants. Nature Publishing Group UK 2022-11-24 /pmc/articles/PMC9700812/ /pubmed/36434030 http://dx.doi.org/10.1038/s41598-022-24302-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Laomettachit, Teeraphan Kraikivski, Pavel Tyson, John J. A continuous-time stochastic Boolean model provides a quantitative description of the budding yeast cell cycle |
title | A continuous-time stochastic Boolean model provides a quantitative description of the budding yeast cell cycle |
title_full | A continuous-time stochastic Boolean model provides a quantitative description of the budding yeast cell cycle |
title_fullStr | A continuous-time stochastic Boolean model provides a quantitative description of the budding yeast cell cycle |
title_full_unstemmed | A continuous-time stochastic Boolean model provides a quantitative description of the budding yeast cell cycle |
title_short | A continuous-time stochastic Boolean model provides a quantitative description of the budding yeast cell cycle |
title_sort | continuous-time stochastic boolean model provides a quantitative description of the budding yeast cell cycle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700812/ https://www.ncbi.nlm.nih.gov/pubmed/36434030 http://dx.doi.org/10.1038/s41598-022-24302-6 |
work_keys_str_mv | AT laomettachitteeraphan acontinuoustimestochasticbooleanmodelprovidesaquantitativedescriptionofthebuddingyeastcellcycle AT kraikivskipavel acontinuoustimestochasticbooleanmodelprovidesaquantitativedescriptionofthebuddingyeastcellcycle AT tysonjohnj acontinuoustimestochasticbooleanmodelprovidesaquantitativedescriptionofthebuddingyeastcellcycle AT laomettachitteeraphan continuoustimestochasticbooleanmodelprovidesaquantitativedescriptionofthebuddingyeastcellcycle AT kraikivskipavel continuoustimestochasticbooleanmodelprovidesaquantitativedescriptionofthebuddingyeastcellcycle AT tysonjohnj continuoustimestochasticbooleanmodelprovidesaquantitativedescriptionofthebuddingyeastcellcycle |