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Exact power spectrum in a minimal hybrid model of stochastic gene expression oscillations

2019/09/21 by Chen Jia, Hong Qian, Jia, Chen +3
Biochemistry, Genetics and Molecular Biology · #34A38 #60H10 #60J25 #92B05 #92C40 #Biological Physics (physics.bio-ph) #Chaotic Dynamics (nlin.CD) #FOS: Biological sciences #FOS: Physical sciences #Gene Regulatory Network Analysis #Molecular Networks (q-bio.MN)

paper · pdf · doi:10.48550/arxiv.1909.09769

openalex publication_date 2019/09/21 · openalex created_date 2019/09/26 · openalex updated_date 2026/07/28

Abstract

Stochastic oscillations in individual cells are usually characterized by a non-monotonic power spectrum with an oscillatory autocorrelation function. Here we develop an analytical approach of stochastic oscillations in a minimal hybrid model of stochastic gene expression including promoter state switching, protein synthesis and degradation, as well as a genetic feedback loop. The oscillations observed in our model are noise-induced since the deterministic theory predicts stable fixed points. The autocorrelated function, power spectrum, and steady-state distribution of protein concentration fluctuations are computed in closed form without making any approximations. Using the exactly solvable model, we illustrate sustained oscillations as a circular motion along a stochastic hysteresis loop induced by gene state switching. A triphasic stochastic bifurcation upon the increasing strength of negative feedback is observed, which reveals how stochastic bursts evolve into stochastic oscillations. In our model, oscillations tend to occur when the protein is relatively stable and when gene switching is relatively slow. Translational bursting is found to enhance the robustness and broaden the region of stochastic oscillations. These results provide deeper insights into R. Thomas' two conjectures for single-cell gene expression kinetics.

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