A spatio-temporal model to reveal oscillatorphenotypes in molecular clocks: Parameterestimation elucidates circadian gene transcriptiondynamics in single-cells
Måns UnossoniD, Marco BrancaccioiD, Michael Harvey HastingsiD, Adam Michael JohanseniD, Bärbel FinkenstädtiD
Abstract
We propose a stochastic distributed delay model together with a Markov random field prior and a measurement model for bioluminescence-reporting to analyse spatiotemporal gene expression in intact networks of cells. The model describes the oscillating time evolution of molecular mRNA counts through a negative transcriptional-translational feedback loop encoded in a chemical Langevin equation with a probabilistic delay distribution. The model is extended spatially by means of a multiplicative random effects model with a first order Markov random field prior distribution. Our methodology effectively separates intrinsic molecular noise, measurement noise, and extrinsic noise and phenotypic variation driving cell heterogeneity, while being amenable to parameter identification and inference. Based on the single-cell model we propose a novel computational stability analysis that allows us to infer two key characteristics, namely the robustness of the oscillations, i.e. whether the reaction network exhibits sustained or damped oscillations, and the profile of the regulation, i.e. whether the inhibition occurs over time in a more distributed versus a more direct manner, which affects the cells ability to phase-shift to new schedules. We show how insight into the spatio-temporal characteristics of the circadian feedback loop in the suprachiasmatic nucleus (SCN) can be gained by applying the methodology to bioluminescence-reported expression of the circadian core clock gene Cry1 across mouse SCN tissue. We find that while (almost) all SCN neurons exhibit robust cell-autonomous oscillations, the parameters that are associated with the regulatory transcription profile give rise to a spatial division of the tissue between the central region whose oscillations are resilient to perturbation in the sense that they maintain a high degree of synchronicity, and the dorsal region which appears to phase shift in a more diversified way as a response to large perturbations and thus could be more amenable to entrainment.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 3
- FWCI
- 0.26
- Field percentile
- 48th percentile
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- The circadian oscillator analysed at the single-transcript level
Nick E. Phillips, Alice Hugues, … Félix Naef·Molecular Systems BiologyPeer-reviewed·Mar 1, 2021
- "Remote and partial clocks expand the circadian neuronal network, driving widespread molecular rhythmicity in Drosophila"
Inés Lucía Patop, Ane Martín Anduaga, … Sebastián Kadener·bioRxiv·Dec 25, 2025
- A spatial model of the plant circadian clock reveals design principles for coordinated timing under noisy environments
M. Greenwood, I. T. Tokuda, J. C. Locke·bioRxiv·Sep 13, 2020
- Weak Coupling Between Intracellular Feedback Loops Explains Dissociation of Clock Gene Dynamics
Christoph Schmal, Daisuke Ono, … Isao T. Tokuda·PLoS Computational BiologyPeer-reviewed·Sep 12, 2019
- Streamlined, cell-specific single-molecule RNA-FISH of core clock mRNAs in clock neurons in whole mount Drosophila brains
Y. Yuan, M. A. Padilla, … S. Yadlapalli·bioRxiv·Sep 5, 2022
- A multiscale model of the mammalian liver circadian clock supports synchronization of autonomous oscillations by intercellular communication.
Daniel Marri, Omar Z. Kana, … Sudin Bhattacharya·bioRxiv·Feb 15, 2024