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A cell size- and cell cycle-aware stochastic model for predicting time-dynamic gene network activity in individual cells
BACKGROUND: Despite the development of various modeling approaches to predict gene network activity, a time dynamic stochastic model taking into account real-time changes in cell volume and cell cycle stages is still missing. RESULTS: Here we present a stochastic single-cell model that can be applie...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673848/ https://www.ncbi.nlm.nih.gov/pubmed/26646617 http://dx.doi.org/10.1186/s12918-015-0240-5 |
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author | Song, Ruijie Peng, Weilin Liu, Ping Acar, Murat |
author_facet | Song, Ruijie Peng, Weilin Liu, Ping Acar, Murat |
author_sort | Song, Ruijie |
collection | PubMed |
description | BACKGROUND: Despite the development of various modeling approaches to predict gene network activity, a time dynamic stochastic model taking into account real-time changes in cell volume and cell cycle stages is still missing. RESULTS: Here we present a stochastic single-cell model that can be applied to any eukaryotic gene network with any number of components. The model tracks changes in cell volume, DNA replication, and cell division, and dynamically adjusts rates of stochastic reactions based on this information. By tracking cell division, the model can maintain cell lineage information, allowing the researcher to trace the descendants of any single cell and therefore study cell lineage effects. To test the predictive power of our model, we applied it to the canonical galactose network of the yeast Saccharomyces cerevisiae. Using a minimal set of free parameters and across several galactose induction conditions, the model effectively captured several details of the experimentally-obtained single-cell network activity levels as well as phenotypic switching rates. CONCLUSION: Our model can readily be customized to model any gene network in any of the commonly used cells types, offering a novel and user-friendly stochastic modeling capability to the systems biology field. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-015-0240-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4673848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46738482015-12-10 A cell size- and cell cycle-aware stochastic model for predicting time-dynamic gene network activity in individual cells Song, Ruijie Peng, Weilin Liu, Ping Acar, Murat BMC Syst Biol Research Article BACKGROUND: Despite the development of various modeling approaches to predict gene network activity, a time dynamic stochastic model taking into account real-time changes in cell volume and cell cycle stages is still missing. RESULTS: Here we present a stochastic single-cell model that can be applied to any eukaryotic gene network with any number of components. The model tracks changes in cell volume, DNA replication, and cell division, and dynamically adjusts rates of stochastic reactions based on this information. By tracking cell division, the model can maintain cell lineage information, allowing the researcher to trace the descendants of any single cell and therefore study cell lineage effects. To test the predictive power of our model, we applied it to the canonical galactose network of the yeast Saccharomyces cerevisiae. Using a minimal set of free parameters and across several galactose induction conditions, the model effectively captured several details of the experimentally-obtained single-cell network activity levels as well as phenotypic switching rates. CONCLUSION: Our model can readily be customized to model any gene network in any of the commonly used cells types, offering a novel and user-friendly stochastic modeling capability to the systems biology field. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-015-0240-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-09 /pmc/articles/PMC4673848/ /pubmed/26646617 http://dx.doi.org/10.1186/s12918-015-0240-5 Text en © Song et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Song, Ruijie Peng, Weilin Liu, Ping Acar, Murat A cell size- and cell cycle-aware stochastic model for predicting time-dynamic gene network activity in individual cells |
title | A cell size- and cell cycle-aware stochastic model for predicting time-dynamic gene network activity in individual cells |
title_full | A cell size- and cell cycle-aware stochastic model for predicting time-dynamic gene network activity in individual cells |
title_fullStr | A cell size- and cell cycle-aware stochastic model for predicting time-dynamic gene network activity in individual cells |
title_full_unstemmed | A cell size- and cell cycle-aware stochastic model for predicting time-dynamic gene network activity in individual cells |
title_short | A cell size- and cell cycle-aware stochastic model for predicting time-dynamic gene network activity in individual cells |
title_sort | cell size- and cell cycle-aware stochastic model for predicting time-dynamic gene network activity in individual cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673848/ https://www.ncbi.nlm.nih.gov/pubmed/26646617 http://dx.doi.org/10.1186/s12918-015-0240-5 |
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