Incorporating spatial diffusion into models of bursty stochastic transcription

The dynamics of gene expression are stochastic and spatial at the molecular scale, with messenger RNA (mRNA) transcribed at specific nuclear locations and then transported to the nuclear boundary for export. Consequently, the spatial distributions of these molecules encode their underlying dynamics. While mechanistic models for molecular counts have revealed numerous insights into gene expression, they have largely neglected now-available subcellular spatial resolution down to individual molecules. Owing to the technical challenges inherent in spatial stochastic processes, tools for studying these subcellular spatial patterns are still limited. Here, we introduce a spatial stochastic model of nuclear mRNA with two-state (telegraph) transcriptional dynamics. Observations of the model can be concisely described as following a spatial Cox process driven by a stochastically switching partial differential equation. We derive analytical solutions for spatial and demographic moments and validate them with simulations. We show that the distribution of mRNA counts can be accurately approximated by a Poisson-beta distribution with tractable parameters, even with complex spatial dynamics. This observation allows for efficient parameter inference demonstrated on synthetic data. Altogether, our work adds progress towards a new frontier of subcellular spatial resolution in inferring the dynamics of gene expression from static snapshot data.

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Publication Details

Journal
Journal of The Royal Society Interface
Published
2025-04-01
DOI
https://doi.org/10.1098/rsif.2024.0739
Citations
10
Primary Topic
Gene Regulatory Network Analysis
Type
article
Field-Weighted Citation Impact
8.06

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article

Incorporating spatial diffusion into models of bursty stochastic transcription

Christopher E. Miles
10 citations
Journal of The Royal Society Interface
Gene Regulatory Network Analysis
8.06
article

Incorporating spatial diffusion into models of bursty stochastic transcription

Christopher E. Miles
article en
10 citations

Abstract

The dynamics of gene expression are stochastic and spatial at the molecular scale, with messenger RNA (mRNA) transcribed at specific nuclear locations and then transported to the nuclear boundary for export. Consequently, the spatial distributions of these molecules encode their underlying dynamics. While mechanistic models for molecular counts have revealed numerous insights into gene expression, they have largely neglected now-available subcellular spatial resolution down to individual molecules. Owing to the technical challenges inherent in spatial stochastic processes, tools for studying these subcellular spatial patterns are still limited. Here, we introduce a spatial stochastic model of nuclear mRNA with two-state (telegraph) transcriptional dynamics. Observations of the model can be concisely described as following a spatial Cox process driven by a stochastically switching partial differential equation. We derive analytical solutions for spatial and demographic moments and validate them with simulations. We show that the distribution of mRNA counts can be accurately approximated by a Poisson-beta distribution with tractable parameters, even with complex spatial dynamics. This observation allows for efficient parameter inference demonstrated on synthetic data. Altogether, our work adds progress towards a new frontier of subcellular spatial resolution in inferring the dynamics of gene expression from static snapshot data.

Journal of The Royal Society InterfaceVol. 22(225)
Division of Mathematical Sciences
Partnerships for the goals
Openalex Percentile: Top 2%
Gene Regulatory Network Analysis
8.06
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Incorporating spatial diffusion into models of bursty stochastic transcription — Christopher E. Miles · Journal of The Royal Society Interface (2025) | TGRS Research Map | TGRS