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Noise Contributions in an Inducible Genetic Switch: A Whole-Cell Simulation Study

Stochastic expression of genes produces heterogeneity in clonal populations of bacteria under identical conditions. We analyze and compare the behavior of the inducible lac genetic switch using well-stirred and spatially resolved simulations for Escherichia coli cells modeled under fast and slow-gro...

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Autores principales: Roberts, Elijah, Magis, Andrew, Ortiz, Julio O., Baumeister, Wolfgang, Luthey-Schulten, Zaida
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053318/
https://www.ncbi.nlm.nih.gov/pubmed/21423716
http://dx.doi.org/10.1371/journal.pcbi.1002010
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author Roberts, Elijah
Magis, Andrew
Ortiz, Julio O.
Baumeister, Wolfgang
Luthey-Schulten, Zaida
author_facet Roberts, Elijah
Magis, Andrew
Ortiz, Julio O.
Baumeister, Wolfgang
Luthey-Schulten, Zaida
author_sort Roberts, Elijah
collection PubMed
description Stochastic expression of genes produces heterogeneity in clonal populations of bacteria under identical conditions. We analyze and compare the behavior of the inducible lac genetic switch using well-stirred and spatially resolved simulations for Escherichia coli cells modeled under fast and slow-growth conditions. Our new kinetic model describing the switching of the lac operon from one phenotype to the other incorporates parameters obtained from recently published in vivo single-molecule fluorescence experiments along with in vitro rate constants. For the well-stirred system, investigation of the intrinsic noise in the circuit as a function of the inducer concentration and in the presence/absence of the feedback mechanism reveals that the noise peaks near the switching threshold. Applying maximum likelihood estimation, we show that the analytic two-state model of gene expression can be used to extract stochastic rates from the simulation data. The simulations also provide mRNA–protein probability landscapes, which demonstrate that switching is the result of crossing both mRNA and protein thresholds. Using cryoelectron tomography of an E. coli cell and data from proteomics studies, we construct spatial in vivo models of cells and quantify the noise contributions and effects on repressor rebinding due to cell structure and crowding in the cytoplasm. Compared to systems without spatial heterogeneity, the model for the fast-growth cells predicts a slight decrease in the overall noise and an increase in the repressors rebinding rate due to anomalous subdiffusion. The tomograms for E. coli grown under slow-growth conditions identify the positions of the ribosomes and the condensed nucleoid. The smaller slow-growth cells have increased mRNA localization and a larger internal inducer concentration, leading to a significant decrease in the lifetime of the repressor–operator complex and an increase in the frequency of transcriptional bursts.
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spelling pubmed-30533182011-03-18 Noise Contributions in an Inducible Genetic Switch: A Whole-Cell Simulation Study Roberts, Elijah Magis, Andrew Ortiz, Julio O. Baumeister, Wolfgang Luthey-Schulten, Zaida PLoS Comput Biol Research Article Stochastic expression of genes produces heterogeneity in clonal populations of bacteria under identical conditions. We analyze and compare the behavior of the inducible lac genetic switch using well-stirred and spatially resolved simulations for Escherichia coli cells modeled under fast and slow-growth conditions. Our new kinetic model describing the switching of the lac operon from one phenotype to the other incorporates parameters obtained from recently published in vivo single-molecule fluorescence experiments along with in vitro rate constants. For the well-stirred system, investigation of the intrinsic noise in the circuit as a function of the inducer concentration and in the presence/absence of the feedback mechanism reveals that the noise peaks near the switching threshold. Applying maximum likelihood estimation, we show that the analytic two-state model of gene expression can be used to extract stochastic rates from the simulation data. The simulations also provide mRNA–protein probability landscapes, which demonstrate that switching is the result of crossing both mRNA and protein thresholds. Using cryoelectron tomography of an E. coli cell and data from proteomics studies, we construct spatial in vivo models of cells and quantify the noise contributions and effects on repressor rebinding due to cell structure and crowding in the cytoplasm. Compared to systems without spatial heterogeneity, the model for the fast-growth cells predicts a slight decrease in the overall noise and an increase in the repressors rebinding rate due to anomalous subdiffusion. The tomograms for E. coli grown under slow-growth conditions identify the positions of the ribosomes and the condensed nucleoid. The smaller slow-growth cells have increased mRNA localization and a larger internal inducer concentration, leading to a significant decrease in the lifetime of the repressor–operator complex and an increase in the frequency of transcriptional bursts. Public Library of Science 2011-03-10 /pmc/articles/PMC3053318/ /pubmed/21423716 http://dx.doi.org/10.1371/journal.pcbi.1002010 Text en Roberts et al. 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
Roberts, Elijah
Magis, Andrew
Ortiz, Julio O.
Baumeister, Wolfgang
Luthey-Schulten, Zaida
Noise Contributions in an Inducible Genetic Switch: A Whole-Cell Simulation Study
title Noise Contributions in an Inducible Genetic Switch: A Whole-Cell Simulation Study
title_full Noise Contributions in an Inducible Genetic Switch: A Whole-Cell Simulation Study
title_fullStr Noise Contributions in an Inducible Genetic Switch: A Whole-Cell Simulation Study
title_full_unstemmed Noise Contributions in an Inducible Genetic Switch: A Whole-Cell Simulation Study
title_short Noise Contributions in an Inducible Genetic Switch: A Whole-Cell Simulation Study
title_sort noise contributions in an inducible genetic switch: a whole-cell simulation study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053318/
https://www.ncbi.nlm.nih.gov/pubmed/21423716
http://dx.doi.org/10.1371/journal.pcbi.1002010
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