Manuel Eduardo Hernández-García, Mariana Gómez-Schiavon, Jorge Velázquez-Castro
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引用次数: 0
Abstract
Gene regulatory networks with negative feedback play a crucial role in conferring robustness and evolutionary resilience to biological systems. However, the discrete nature of molecular components and probabilistic interactions in these networks are inherently subject to fluctuations, which pose challenges for stability analysis. Traditional analysis methods for stochastic systems, like the Langevin equation and the Fokker-Planck equation, are widely used. However, these methods primarily provide approximations of system behavior and may not be suitable for systems that exhibit non-mass-action kinetics, such as those described by Hill functions. In this study, we employed a second-moment approach to analyze the stability of a gene regulatory network with negative feedback under intrinsic fluctuations. By transforming the stochastic system into a set of ordinary differential equations for the mean concentration and second central moment, we performed a stability analysis similar to that used in deterministic models, where there are no fluctuations. Our results show that the incorporation of the second central moment introduces two additional negative eigenvalues, indicating that the system remains stable under intrinsic fluctuations. Furthermore, the stability of the second central moment suggests that the fluctuations do not induce instability in the system. The stationary values of the mean concentrations were found to be the same as those in the deterministic case, indicating that fluctuations did not influence stationary mean concentrations. This framework provides a practical and insightful method for analyzing the stability of stochastic systems and can be extended to other biochemical networks with regulatory feedback and intrinsic fluctuations through a framework of ordinary differential equations.
期刊介绍:
Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity.
Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as:
molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions
subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure
intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division
systems biology, e.g. signaling, gene regulation and metabolic networks
cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms
cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis
cell-cell interactions, cell aggregates, organoids, tissues and organs
developmental dynamics, including pattern formation and morphogenesis
physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation
neuronal systems, including information processing by networks, memory and learning
population dynamics, ecology, and evolution
collective action and emergence of collective phenomena.