TY - JOUR
T1 - Efficient approximations of transcriptional bursting effects on the dynamics of a gene regulatory network
AU - Kursawe, Jochen
AU - Moneyron, Antoine
AU - Galla, Tobias
N1 - Funding: This work was partially supported by the María de Maeztu project CEX2021-001164-M funded by the MICIU/AEI/10.13039/501100011033. AM acknowledges the support of the ERC EU project 856408-STUOD and benefit from the support of the French government "Investissements d'Avenir'' program ANR-11-LABX-0020-01.
PY - 2025/6/25
Y1 - 2025/6/25
N2 - Mathematical models of gene regulatory networks are widely used to study cell fate changes and transcriptional regulation. When designing such models, it is important to accurately account for sources of stochasticity. However, doing so can be computationally expensive and analytically untractable, posing limits on the extent of our explorations and on parameter inference. Here, we explore this challenge using the example of a simple auto-negative feedback motif, in which we incorporate stochastic variation due to transcriptional bursting and noise from finite copy numbers. We find that transcriptional bursting may change the qualitative dynamics of the system by inducing oscillations when they would not otherwise be present, or by magnifying existing oscillations. We describe multiple levels of approximation for the model in the form of differential equations, piecewise-deterministic processes and stochastic differential equations. Importantly, we derive how the classical chemical Langevin equation can be extended to include a noise term representing transcriptional bursting. This approximation drastically decreases computation times and allows us to analytically calculate properties of the dynamics, such as their power spectrum. We explore when these approximations break down and provide recommendations for their use. Our analysis illustrates the importance of accounting for transcriptional bursting when simulating gene regulatory network dynamics and provides recommendations to do so with computationally efficient methods.
AB - Mathematical models of gene regulatory networks are widely used to study cell fate changes and transcriptional regulation. When designing such models, it is important to accurately account for sources of stochasticity. However, doing so can be computationally expensive and analytically untractable, posing limits on the extent of our explorations and on parameter inference. Here, we explore this challenge using the example of a simple auto-negative feedback motif, in which we incorporate stochastic variation due to transcriptional bursting and noise from finite copy numbers. We find that transcriptional bursting may change the qualitative dynamics of the system by inducing oscillations when they would not otherwise be present, or by magnifying existing oscillations. We describe multiple levels of approximation for the model in the form of differential equations, piecewise-deterministic processes and stochastic differential equations. Importantly, we derive how the classical chemical Langevin equation can be extended to include a noise term representing transcriptional bursting. This approximation drastically decreases computation times and allows us to analytically calculate properties of the dynamics, such as their power spectrum. We explore when these approximations break down and provide recommendations for their use. Our analysis illustrates the importance of accounting for transcriptional bursting when simulating gene regulatory network dynamics and provides recommendations to do so with computationally efficient methods.
KW - Gene regulatory networks
KW - Gene expression oscillations
KW - Transcriptional bursting
KW - Fast-switching environments
KW - Piecewise-deterministic Markov processes
KW - Chemical Langevin equations
U2 - 10.1098/rsif.2025.0170
DO - 10.1098/rsif.2025.0170
M3 - Article
SN - 1742-5689
VL - 22
JO - Journal of the Royal Society Interface
JF - Journal of the Royal Society Interface
IS - 227
M1 - 20250170
ER -