Markovian Promoter Models: A Mechanistic Alternative to Hill Functions in Gene Regulatory Networks

Fuente: arXiv
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Autor principal: Wu, Tianyu
Formato: Preprint
Publicado: 2025
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author Wu, Tianyu
author_facet Wu, Tianyu
contents Gene regulatory networks are typically modeled using ordinary differential equations (ODEs) with phenomenological Hill functions to represent transcriptional regulation. While computationally efficient, Hill functions lack mechanistic grounding and cannot capture stochastic promoter dynamics. We present a hybrid Markovian-ODE framework that explicitly models discrete promoter states while maintaining computational tractability. Uniquely, we parameterize this model using fractional dwell times derived from ChEC-seq data, enabling the inference of in vivo kinetic rates from steady-state chromatin profiling. Our approach tracks individual transcription factor binding events as a continuous-time Markov chain, linked to deterministic molecular dynamics. We validate this framework on seven gene regulatory systems spanning basic to advanced complexity: the GAL system, repressilator, Goodwin oscillator, toggle switch, incoherent feed-forward loop, p53-Mdm2 oscillator, and NF-$κ$B pathway. Comparison with stochastic simulation algorithm (SSA) ground truth demonstrates that Markovian promoter models achieve similar accuracy to full stochastic simulations while being 10-100$\times$ faster. Our framework provides a mechanistic foundation for gene regulation modeling and enables investigation of promoter-level stochasticity in complex regulatory networks.
format Preprint
id arxiv_https___arxiv_org_abs_2512_18442
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Markovian Promoter Models: A Mechanistic Alternative to Hill Functions in Gene Regulatory Networks
Wu, Tianyu
Molecular Networks
Quantitative Methods
Gene regulatory networks are typically modeled using ordinary differential equations (ODEs) with phenomenological Hill functions to represent transcriptional regulation. While computationally efficient, Hill functions lack mechanistic grounding and cannot capture stochastic promoter dynamics. We present a hybrid Markovian-ODE framework that explicitly models discrete promoter states while maintaining computational tractability. Uniquely, we parameterize this model using fractional dwell times derived from ChEC-seq data, enabling the inference of in vivo kinetic rates from steady-state chromatin profiling. Our approach tracks individual transcription factor binding events as a continuous-time Markov chain, linked to deterministic molecular dynamics. We validate this framework on seven gene regulatory systems spanning basic to advanced complexity: the GAL system, repressilator, Goodwin oscillator, toggle switch, incoherent feed-forward loop, p53-Mdm2 oscillator, and NF-$κ$B pathway. Comparison with stochastic simulation algorithm (SSA) ground truth demonstrates that Markovian promoter models achieve similar accuracy to full stochastic simulations while being 10-100$\times$ faster. Our framework provides a mechanistic foundation for gene regulation modeling and enables investigation of promoter-level stochasticity in complex regulatory networks.
title Markovian Promoter Models: A Mechanistic Alternative to Hill Functions in Gene Regulatory Networks
topic Molecular Networks
Quantitative Methods
url https://arxiv.org/abs/2512.18442