| Autor: |
Braichenko S; School of Biological Sciences, University of Edinburgh, Edinburgh, UK.; School of Informatics, University of Edinburgh, Edinburgh, UK., Holehouse J; School of Biological Sciences, University of Edinburgh, Edinburgh, UK., Grima R; School of Biological Sciences, University of Edinburgh, Edinburgh, UK. |
| Jazyk: |
angličtina |
| Zdroj: |
Journal of the Royal Society, Interface [J R Soc Interface] 2021 Oct; Vol. 18 (183), pp. 20210510. Date of Electronic Publication: 2021 Oct 06. |
| DOI: |
10.1098/rsif.2021.0510 |
| Abstrakt: |
Two-state models (telegraph-like models) have a successful history of predicting distributions of cellular and nascent mRNA numbers that can well fit experimental data. These models exclude key rate limiting steps, and hence it is unclear why they are able to accurately predict the number distributions. To answer this question, here we compare these models to a novel stochastic mechanistic model of transcription in mammalian cells that presents a unified description of transcriptional factor, polymerase and mature mRNA dynamics. We show that there is a large region of parameter space where the first, second and third moments of the distributions of the waiting times between two consecutively produced transcripts (nascent or mature) of two-state and mechanistic models exactly match. In this region: (i) one can uniquely express the two-state model parameters in terms of those of the mechanistic model, (ii) the models are practically indistinguishable by comparison of their transcript numbers distributions, and (iii) they are distinguishable from the shape of their waiting time distributions. Our results clarify the relationship between different gene expression models and identify a means to select between them from experimental data. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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