Dose response relationship in anti-stress gene regulatory networks.

To maintain a stable intracellular environment, cells utilize complex and specialized defense systems against a variety of external perturbations, such as electrophilic stress, heat shock, and hypoxia, etc. Irrespective of the type of stress, many adaptive mechanisms contributing to cellular homeost...

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Main Authors: Qiang Zhang, Melvin E Andersen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2007-03-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC1808489?pdf=render
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author Qiang Zhang
Melvin E Andersen
author_facet Qiang Zhang
Melvin E Andersen
author_sort Qiang Zhang
collection DOAJ
description To maintain a stable intracellular environment, cells utilize complex and specialized defense systems against a variety of external perturbations, such as electrophilic stress, heat shock, and hypoxia, etc. Irrespective of the type of stress, many adaptive mechanisms contributing to cellular homeostasis appear to operate through gene regulatory networks that are organized into negative feedback loops. In general, the degree of deviation of the controlled variables, such as electrophiles, misfolded proteins, and O2, is first detected by specialized sensor molecules, then the signal is transduced to specific transcription factors. Transcription factors can regulate the expression of a suite of anti-stress genes, many of which encode enzymes functioning to counteract the perturbed variables. The objective of this study was to explore, using control theory and computational approaches, the theoretical basis that underlies the steady-state dose response relationship between cellular stressors and intracellular biochemical species (controlled variables, transcription factors, and gene products) in these gene regulatory networks. Our work indicated that the shape of dose response curves (linear, superlinear, or sublinear) depends on changes in the specific values of local response coefficients (gains) distributed in the feedback loop. Multimerization of anti-stress enzymes and transcription factors into homodimers, homotrimers, or even higher-order multimers, play a significant role in maintaining robust homeostasis. Moreover, our simulation noted that dose response curves for the controlled variables can transition sequentially through four distinct phases as stressor level increases: initial superlinear with lesser control, superlinear more highly controlled, linear uncontrolled, and sublinear catastrophic. Each phase relies on specific gain-changing events that come into play as stressor level increases. The low-dose region is intrinsically nonlinear, and depending on the level of local gains, presence of gain-changing events, and degree of feedforward gene activation, this region can appear as superlinear, sublinear, or even J-shaped. The general dose response transition proposed here was further examined in a complex anti-electrophilic stress pathway, which involves multiple genes, enzymes, and metabolic reactions. This work would help biologists and especially toxicologists to better assess and predict the cellular impact brought about by biological stressors.
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spelling doaj.art-9fe20535ef724044835a7cc0096a13522022-12-21T22:38:40ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582007-03-0133e2410.1371/journal.pcbi.0030024Dose response relationship in anti-stress gene regulatory networks.Qiang ZhangMelvin E AndersenTo maintain a stable intracellular environment, cells utilize complex and specialized defense systems against a variety of external perturbations, such as electrophilic stress, heat shock, and hypoxia, etc. Irrespective of the type of stress, many adaptive mechanisms contributing to cellular homeostasis appear to operate through gene regulatory networks that are organized into negative feedback loops. In general, the degree of deviation of the controlled variables, such as electrophiles, misfolded proteins, and O2, is first detected by specialized sensor molecules, then the signal is transduced to specific transcription factors. Transcription factors can regulate the expression of a suite of anti-stress genes, many of which encode enzymes functioning to counteract the perturbed variables. The objective of this study was to explore, using control theory and computational approaches, the theoretical basis that underlies the steady-state dose response relationship between cellular stressors and intracellular biochemical species (controlled variables, transcription factors, and gene products) in these gene regulatory networks. Our work indicated that the shape of dose response curves (linear, superlinear, or sublinear) depends on changes in the specific values of local response coefficients (gains) distributed in the feedback loop. Multimerization of anti-stress enzymes and transcription factors into homodimers, homotrimers, or even higher-order multimers, play a significant role in maintaining robust homeostasis. Moreover, our simulation noted that dose response curves for the controlled variables can transition sequentially through four distinct phases as stressor level increases: initial superlinear with lesser control, superlinear more highly controlled, linear uncontrolled, and sublinear catastrophic. Each phase relies on specific gain-changing events that come into play as stressor level increases. The low-dose region is intrinsically nonlinear, and depending on the level of local gains, presence of gain-changing events, and degree of feedforward gene activation, this region can appear as superlinear, sublinear, or even J-shaped. The general dose response transition proposed here was further examined in a complex anti-electrophilic stress pathway, which involves multiple genes, enzymes, and metabolic reactions. This work would help biologists and especially toxicologists to better assess and predict the cellular impact brought about by biological stressors.http://europepmc.org/articles/PMC1808489?pdf=render
spellingShingle Qiang Zhang
Melvin E Andersen
Dose response relationship in anti-stress gene regulatory networks.
PLoS Computational Biology
title Dose response relationship in anti-stress gene regulatory networks.
title_full Dose response relationship in anti-stress gene regulatory networks.
title_fullStr Dose response relationship in anti-stress gene regulatory networks.
title_full_unstemmed Dose response relationship in anti-stress gene regulatory networks.
title_short Dose response relationship in anti-stress gene regulatory networks.
title_sort dose response relationship in anti stress gene regulatory networks
url http://europepmc.org/articles/PMC1808489?pdf=render
work_keys_str_mv AT qiangzhang doseresponserelationshipinantistressgeneregulatorynetworks
AT melvineandersen doseresponserelationshipinantistressgeneregulatorynetworks