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Modular Design of Artificial Tissue Homeostasis: Robust Control through Synthetic Cellular Heterogeneity
Synthetic biology efforts have largely focused on small engineered gene networks, yet understanding how to integrate multiple synthetic modules and interface them with endogenous pathways remains a challenge. Here we present the design, system integration, and analysis of several large scale synthet...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400602/ https://www.ncbi.nlm.nih.gov/pubmed/22829755 http://dx.doi.org/10.1371/journal.pcbi.1002579 |
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author | Miller, Miles Hafner, Marc Sontag, Eduardo Davidsohn, Noah Subramanian, Sairam Purnick, Priscilla E. M. Lauffenburger, Douglas Weiss, Ron |
author_facet | Miller, Miles Hafner, Marc Sontag, Eduardo Davidsohn, Noah Subramanian, Sairam Purnick, Priscilla E. M. Lauffenburger, Douglas Weiss, Ron |
author_sort | Miller, Miles |
collection | PubMed |
description | Synthetic biology efforts have largely focused on small engineered gene networks, yet understanding how to integrate multiple synthetic modules and interface them with endogenous pathways remains a challenge. Here we present the design, system integration, and analysis of several large scale synthetic gene circuits for artificial tissue homeostasis. Diabetes therapy represents a possible application for engineered homeostasis, where genetically programmed stem cells maintain a steady population of β-cells despite continuous turnover. We develop a new iterative process that incorporates modular design principles with hierarchical performance optimization targeted for environments with uncertainty and incomplete information. We employ theoretical analysis and computational simulations of multicellular reaction/diffusion models to design and understand system behavior, and find that certain features often associated with robustness (e.g., multicellular synchronization and noise attenuation) are actually detrimental for tissue homeostasis. We overcome these problems by engineering a new class of genetic modules for ‘synthetic cellular heterogeneity’ that function to generate beneficial population diversity. We design two such modules (an asynchronous genetic oscillator and a signaling throttle mechanism), demonstrate their capacity for enhancing robust control, and provide guidance for experimental implementation with various computational techniques. We found that designing modules for synthetic heterogeneity can be complex, and in general requires a framework for non-linear and multifactorial analysis. Consequently, we adapt a ‘phenotypic sensitivity analysis’ method to determine how functional module behaviors combine to achieve optimal system performance. We ultimately combine this analysis with Bayesian network inference to extract critical, causal relationships between a module's biochemical rate-constants, its high level functional behavior in isolation, and its impact on overall system performance once integrated. |
format | Online Article Text |
id | pubmed-3400602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34006022012-07-24 Modular Design of Artificial Tissue Homeostasis: Robust Control through Synthetic Cellular Heterogeneity Miller, Miles Hafner, Marc Sontag, Eduardo Davidsohn, Noah Subramanian, Sairam Purnick, Priscilla E. M. Lauffenburger, Douglas Weiss, Ron PLoS Comput Biol Research Article Synthetic biology efforts have largely focused on small engineered gene networks, yet understanding how to integrate multiple synthetic modules and interface them with endogenous pathways remains a challenge. Here we present the design, system integration, and analysis of several large scale synthetic gene circuits for artificial tissue homeostasis. Diabetes therapy represents a possible application for engineered homeostasis, where genetically programmed stem cells maintain a steady population of β-cells despite continuous turnover. We develop a new iterative process that incorporates modular design principles with hierarchical performance optimization targeted for environments with uncertainty and incomplete information. We employ theoretical analysis and computational simulations of multicellular reaction/diffusion models to design and understand system behavior, and find that certain features often associated with robustness (e.g., multicellular synchronization and noise attenuation) are actually detrimental for tissue homeostasis. We overcome these problems by engineering a new class of genetic modules for ‘synthetic cellular heterogeneity’ that function to generate beneficial population diversity. We design two such modules (an asynchronous genetic oscillator and a signaling throttle mechanism), demonstrate their capacity for enhancing robust control, and provide guidance for experimental implementation with various computational techniques. We found that designing modules for synthetic heterogeneity can be complex, and in general requires a framework for non-linear and multifactorial analysis. Consequently, we adapt a ‘phenotypic sensitivity analysis’ method to determine how functional module behaviors combine to achieve optimal system performance. We ultimately combine this analysis with Bayesian network inference to extract critical, causal relationships between a module's biochemical rate-constants, its high level functional behavior in isolation, and its impact on overall system performance once integrated. Public Library of Science 2012-07-19 /pmc/articles/PMC3400602/ /pubmed/22829755 http://dx.doi.org/10.1371/journal.pcbi.1002579 Text en Miller 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 Miller, Miles Hafner, Marc Sontag, Eduardo Davidsohn, Noah Subramanian, Sairam Purnick, Priscilla E. M. Lauffenburger, Douglas Weiss, Ron Modular Design of Artificial Tissue Homeostasis: Robust Control through Synthetic Cellular Heterogeneity |
title | Modular Design of Artificial Tissue Homeostasis: Robust Control through Synthetic Cellular Heterogeneity |
title_full | Modular Design of Artificial Tissue Homeostasis: Robust Control through Synthetic Cellular Heterogeneity |
title_fullStr | Modular Design of Artificial Tissue Homeostasis: Robust Control through Synthetic Cellular Heterogeneity |
title_full_unstemmed | Modular Design of Artificial Tissue Homeostasis: Robust Control through Synthetic Cellular Heterogeneity |
title_short | Modular Design of Artificial Tissue Homeostasis: Robust Control through Synthetic Cellular Heterogeneity |
title_sort | modular design of artificial tissue homeostasis: robust control through synthetic cellular heterogeneity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400602/ https://www.ncbi.nlm.nih.gov/pubmed/22829755 http://dx.doi.org/10.1371/journal.pcbi.1002579 |
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