Exploring the spatio–temporal dynamics in activator–inhibitor systems through a dual approach of analysis and computation

dc.contributor.authorChiteri, Vincent Nandwa
dc.contributor.authorJuma, Victor Ogesa
dc.contributor.authorOkwoyo, James Mariita
dc.contributor.authorMoindi, Stephen Kibet
dc.contributor.authorMapfumo, Kudzanayi Zebedia
dc.contributor.authorMadzvamuse, Anotida
dc.date.accessioned2026-02-19T04:38:49Z
dc.date.available2026-02-19T04:38:49Z
dc.date.issued2025-07
dc.descriptionDATA AVAILABILITY : The current manuscript includes all the data supporting the findings of this study.
dc.description.abstractReal-world mathematical models often manifest as systems of non-linear differential equations, which presents challenges in obtaining closed-form analytical solutions. In this paper, we study the diffusion-driven instability of an activator-inhibitor-type reaction-diffusion (RD) system modeling the GEF-Rho-Myosin signaling pathway linked to cellular contractility. The mathematical model we study is formulated from first principles using experimental observations. The model formulation is based on the biological and mathematical assumptions. The novelty is the incorporation of Myo9b as a GAP for RhoA, leading to a new mathematical model that describes Rho activity dynamics linked to cell contraction dynamics. Assuming mass conservation of molecular species and adopting a quasi-steady state assumption based on biological observations, model reduction is undertaken and leads us to a system of two equations. We adopt a dual approach of mathematical analysis and numerical computations to study the spatiotemporal dynamics of the system. First, in absence of diffusion, we use a combination of phase-plane analysis, numerical bifurcation and simulations to characterize the temporal dynamics of the model. In the absence of spatial variations, we identified two sets of parameters where the model exhibit different transition dynamics. For some set of parameters, the model transitions from stable to oscillatory and back to stable, while for another set, the model dynamics transition from stable to bistable and back to stable dynamics. To study the effect of parameter variation on model solutions, we use partial rank correlation coefficient (PRCC) to characterize the sensitivity of the model steady states with respect to parameters. Second, we extend the analysis of the model by studying conditions under which a uniform steady state becomes unstable in the presence of spatial variations, in a process known as Turing diffusion-driven instability. By exploiting the necessary conditions for diffusion-driven instability and the sufficient conditions for pattern formation we carry out, numerically, parameter estimation through the use of mode isolation. To support theoretical and computational findings, we employ the pdepe solver in one-space dimension and the finite difference method in two-space dimension.
dc.description.departmentMathematics and Applied Mathematics
dc.description.librarianam2026
dc.description.sdgSDG-04: Quality education
dc.description.sponsorshipFinancial support from The European Simons Foundation, the Pacific Institute for the Mathematical Sciences (PIMS), Canada, and the UBC Mathematics Department; partly supported by the EPSRC, United Kingdom, the European Union Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 642866, the Commission for Developing Countries, and the Simons Foundation; the Royal Society Wolfson Research Merit Award funded generously by the Wolfson Foundation, United Kingdom; supported by the Canada Research Chair (Tier 1) in Theoretical and Computational Biology, the Natural Sciences and Engineering Research Council of Canada (NSERC), Discovery Grants Program, the British Columbia Knowledge Development Fund (BCKDF), Canada, Canada Foundation for Innovation – John R. Evans Leaders Fund – Partnerships (CFI-JELF), the British Columbia Foundation for Non-Animal Research, and the UKRI En-gineering and Physical Sciences Research Council, United Kingdom.
dc.description.urihttps://www.sciencedirect.com/journal/mathematical-biosciences
dc.identifier.citationChiteri, V.N., Juma, V.O., Okwoyo, J.M. et al. 2025, 'Exploring the spatio–temporal dynamics in activator–inhibitor systems through a dual approach of analysis and computation', Mathematical Biosciences, vol. 385, art. 109449, pp. 1-20. https://doi.org/10.1016/j.mbs.2025.109449.
dc.identifier.issn0025-5564 (print)
dc.identifier.issn1879-3134 (online)
dc.identifier.other10.1016/j.mbs.2025.109449
dc.identifier.urihttp://hdl.handle.net/2263/108431
dc.language.isoen
dc.publisherElsevier
dc.rights© 2025 The Author(s). This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND).
dc.subjectDiffusion-driven instability
dc.subjectPattern formation
dc.subjectReaction–diffusion system
dc.subjectLinear stability analysis
dc.subjectMass conservation
dc.subjectGEF-Rho-Myosin signaling network
dc.subjectActivator–inhibitor systems
dc.subjectLocally asymptotically stable
dc.subjectFinite difference method
dc.subjectMode isolation
dc.subjectSensitivity analysis
dc.titleExploring the spatio–temporal dynamics in activator–inhibitor systems through a dual approach of analysis and computation
dc.typeArticle

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