Projects per year
Abstract / Description of output
Transcriptional bursting is a major source of noise in gene expression. The telegraph model of gene expression, whereby transcription switches between \on" and \off" states, is the dominant model for bursting. Recently it was shown that the telegraph model cannot explain a number of experimental observations from perturbation data. Here we study an alternative model that is consistent with the data and which explicitly describes RNA polymerase recruitment and polymerase pause release, two steps necessary form RNA production. We derive the exact steady-state distribution of mRNA numbers and an approximate steady-state distribution of protein numbers which are given by generalized hypergeometric functions. The theory is used to calculate the relative sensitivity of the coefficient of variation of mRNA fluctuations for thousands of genes in mouse broblasts. This indicates that the size of fluctuations is mostly sensitive to the rate of burst initiation and the mRNA degradation rate. Furthermore we show that (i) the time-dependent distribution of mRNA numbers is accurately approximated by a modified telegraph model with a Michaelis-Menten like dependence of the effective transcription rate on RNA polymerase abundance. (ii) the model predicts that if the polymerase recruitment rate is comparable or less than the pause release rate, then upon gene replication the mean number of RNA per cell remains approximately constant. This gene dosage compensation property has been experimentally observed and cannot be explained by the telegraph model with constant rates.
Original language | English |
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Number of pages | 15 |
Journal | Biophysical Journal |
Early online date | 3 Aug 2020 |
DOIs | |
Publication status | E-pub ahead of print - 3 Aug 2020 |
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Dive into the research topics of 'A stochastic model of gene expression with polymerase recruitment and pause release'. Together they form a unique fingerprint.Projects
- 2 Finished
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Bilateral NSF/BIO-BBSRC: Modelling Light Control of Development
Halliday, K., Grima, R., Furniss, J., Seaton, D. & Urquiza garcía, J.
1/09/15 → 31/03/19
Project: Research
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SynthSys-Mammalian: Edinburgh Mammalian Synthetic Biology Research Centre
Rosser, S., Bird, A., Cai, Y., Earnshaw, B., Millar, A., Molina, N., Pilizota, T., Swain, P. & Waites, W.
14/11/14 → 31/03/22
Project: Research