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Are Quasi-Steady-State Approximated Models Suitable for Quantifying Intrinsic Noise Accurately?
Large gene regulatory networks (GRN) are often modeled with quasi-steady-state approximation (QSSA) to reduce the huge computational time required for intrinsic noise quantification using Gillespie stochastic simulation algorithm (SSA). However, the question still remains whether the stochastic QSSA...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4556639/ https://www.ncbi.nlm.nih.gov/pubmed/26327626 http://dx.doi.org/10.1371/journal.pone.0136668 |
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author | Sengupta, Dola Kar, Sandip |
author_facet | Sengupta, Dola Kar, Sandip |
author_sort | Sengupta, Dola |
collection | PubMed |
description | Large gene regulatory networks (GRN) are often modeled with quasi-steady-state approximation (QSSA) to reduce the huge computational time required for intrinsic noise quantification using Gillespie stochastic simulation algorithm (SSA). However, the question still remains whether the stochastic QSSA model measures the intrinsic noise as accurately as the SSA performed for a detailed mechanistic model or not? To address this issue, we have constructed mechanistic and QSSA models for few frequently observed GRNs exhibiting switching behavior and performed stochastic simulations with them. Our results strongly suggest that the performance of a stochastic QSSA model in comparison to SSA performed for a mechanistic model critically relies on the absolute values of the mRNA and protein half-lives involved in the corresponding GRN. The extent of accuracy level achieved by the stochastic QSSA model calculations will depend on the level of bursting frequency generated due to the absolute value of the half-life of either mRNA or protein or for both the species. For the GRNs considered, the stochastic QSSA quantifies the intrinsic noise at the protein level with greater accuracy and for larger combinations of half-life values of mRNA and protein, whereas in case of mRNA the satisfactory accuracy level can only be reached for limited combinations of absolute values of half-lives. Further, we have clearly demonstrated that the abundance levels of mRNA and protein hardly matter for such comparison between QSSA and mechanistic models. Based on our findings, we conclude that QSSA model can be a good choice for evaluating intrinsic noise for other GRNs as well, provided we make a rational choice based on experimental half-life values available in literature. |
format | Online Article Text |
id | pubmed-4556639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45566392015-09-10 Are Quasi-Steady-State Approximated Models Suitable for Quantifying Intrinsic Noise Accurately? Sengupta, Dola Kar, Sandip PLoS One Research Article Large gene regulatory networks (GRN) are often modeled with quasi-steady-state approximation (QSSA) to reduce the huge computational time required for intrinsic noise quantification using Gillespie stochastic simulation algorithm (SSA). However, the question still remains whether the stochastic QSSA model measures the intrinsic noise as accurately as the SSA performed for a detailed mechanistic model or not? To address this issue, we have constructed mechanistic and QSSA models for few frequently observed GRNs exhibiting switching behavior and performed stochastic simulations with them. Our results strongly suggest that the performance of a stochastic QSSA model in comparison to SSA performed for a mechanistic model critically relies on the absolute values of the mRNA and protein half-lives involved in the corresponding GRN. The extent of accuracy level achieved by the stochastic QSSA model calculations will depend on the level of bursting frequency generated due to the absolute value of the half-life of either mRNA or protein or for both the species. For the GRNs considered, the stochastic QSSA quantifies the intrinsic noise at the protein level with greater accuracy and for larger combinations of half-life values of mRNA and protein, whereas in case of mRNA the satisfactory accuracy level can only be reached for limited combinations of absolute values of half-lives. Further, we have clearly demonstrated that the abundance levels of mRNA and protein hardly matter for such comparison between QSSA and mechanistic models. Based on our findings, we conclude that QSSA model can be a good choice for evaluating intrinsic noise for other GRNs as well, provided we make a rational choice based on experimental half-life values available in literature. Public Library of Science 2015-09-01 /pmc/articles/PMC4556639/ /pubmed/26327626 http://dx.doi.org/10.1371/journal.pone.0136668 Text en © 2015 Sengupta, Kar http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Sengupta, Dola Kar, Sandip Are Quasi-Steady-State Approximated Models Suitable for Quantifying Intrinsic Noise Accurately? |
title | Are Quasi-Steady-State Approximated Models Suitable for Quantifying Intrinsic Noise Accurately? |
title_full | Are Quasi-Steady-State Approximated Models Suitable for Quantifying Intrinsic Noise Accurately? |
title_fullStr | Are Quasi-Steady-State Approximated Models Suitable for Quantifying Intrinsic Noise Accurately? |
title_full_unstemmed | Are Quasi-Steady-State Approximated Models Suitable for Quantifying Intrinsic Noise Accurately? |
title_short | Are Quasi-Steady-State Approximated Models Suitable for Quantifying Intrinsic Noise Accurately? |
title_sort | are quasi-steady-state approximated models suitable for quantifying intrinsic noise accurately? |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4556639/ https://www.ncbi.nlm.nih.gov/pubmed/26327626 http://dx.doi.org/10.1371/journal.pone.0136668 |
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