Abstract
BackgroundGene expression is known to be an intrinsically stochastic process which can involve single-digit numbers of mRNA molecules in a cell at any given time. The modelling of such processes calls for the use of exact stochastic simulation methods, most notably the Gillespie algorithm. However, this stochasticity, also termed “intrinsic noise”, does not account for all the variability between genetically identical cells growing in a homogeneous environment.Despite substantial experimental efforts, determining appropriate model parameters continues to be a challenge. Methods based on approximate Bayesian computation can be used to obtain posterior parameter distributions given the observed data. However, such inference procedures require large numbers of simulations of the model and exact stochastic simulation is computationally costly.In this work we focus on the specific case of trying to infer model parameters describing reaction rates and extrinsic noise on the basis of measurements of molecule numbers in individual cells at a given time point.ResultsTo make the problem computationally tractable we develop an exact, model-specific, stochastic simulation algorithm for the commonly used two-state model of gene expression. This algorithm relies on certain assumptions and favourable properties of the model to forgo the simulation of the whole temporal trajectory of protein numbers in the system, instead returning only the number of protein and mRNA molecules present in the system at a specified time point. The computational gain is proportional to the number of protein molecules created in the system and becomes significant for systems involving hundreds or thousands of protein molecules.ConclusionsWe employ this simulation algorithm with approximate Bayesian computation to jointly infer the model’s rate and noise parameters from published gene expression data. Our analysis indicates that for most genes the extrinsic contributions to noise will be small to moderate but certainly are non-negligible.Electronic supplementary materialThe online version of this article (doi:10.1186/s12918-016-0324-x) contains supplementary material, which is available to authorized users.
Highlights
Gene expression is known to be an intrinsically stochastic process which can involve single-digit numbers of mRNA molecules in a cell at any given time
We develop a model-specific simulation method which takes advantage of the Poissonian relationship between the number of surviving protein molecules produced from a given mRNA molecule and its lifetime, under certain assumptions
Posterior distributions of parameters We begin our analysis by examining the posterior distributions of parameters obtained for each gene using the approximate Bayesian computation (ABC) Sequential Monte Carlo (ABC-sequential Monte Carlo (SMC)) inference procedure
Summary
Gene expression is known to be an intrinsically stochastic process which can involve single-digit numbers of mRNA molecules in a cell at any given time. The modelling of such processes calls for the use of exact stochastic simulation methods, most notably the Gillespie algorithm. This stochasticity, termed “intrinsic noise”, does not account for all the variability between genetically identical cells growing in a homogeneous environment. Methods based on approximate Bayesian computation can be used to obtain posterior parameter distributions given the observed data Such inference procedures require large numbers of simulations of the model and exact stochastic simulation is computationally costly. Extrinsic variability has been modelled by linking the perturbation of model parameters to perturbation of the model output using a range of methods, including the Unscented Transform [12] the method of moment closure [13], and density estimation [14]
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.