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Cameron Hopkinson

Publications and source records attributed to Cameron Hopkinson.

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Approximate Analytical Protein Distributions for the Three-stage Model of Stochastic Gene Expression

Gene expression is an intrinsically stochastic process that generates phenotypic heterogeneity within genetically identical cell populations. While the exact statistical moments of the protein count can be obtained for a broad range of complex models, the corresponding distributions are significantly harder to obtain and intractable in many cases. The classical three-stage model of gene expression, which predicts fluctuations in protein levels as a function of promoter switching, transcription, translation, and degradation events all occurring with linear propensities, illustrates this perfectly; deriving its exact protein distribution remains elusive. Here, using the partitioning property of time-inhomogeneous Poisson processes, we develop an exact mapping of the three-stage model onto a simplified model. The simplified model allows us to formulate two analytical approximations for the full protein distribution of the three-stage model based on a beta-mixture representation of the exact solution for a simpler model. We show that the two approximations are asymptotically exact in different limiting cases and verify their accuracy against simulations for a broad range of parameters. Although approximate, these are the first analytical expressions for protein distributions for the three-stage model that are highly accurate in intermediate regimes.

q-bio.QM

Post-transcriptional Regulation of Stochastic Gene Expression Conditioned on Large Deviations

Gene expression is a stochastic process that gives rise to large fluctuations in protein levels leading to phenotypic heterogeneity in clonal cell populations; post-transcriptional regulation plays a crucial role in controlling the level of phenotypic variability within a population, which is directly tied to cell-fate decisions. As such, substantial efforts have been directed towards quantitatively modeling the effects of various post-transcriptional mechanisms on the strength of fluctuations in protein levels (noise). However, the corresponding effects of post-transcriptional regulation on the occurrence of rare events corresponding to large deviations are far less explored and have only been considered for a special model. Here, we take a general model of post-transcriptional regulation and apply the partitioning of Poisson arrivals (PPA) framework to map it onto a model that resembles promoter-based regulation of transcription, leading to a general framework to obtain objects of interest in large deviations (i.e. large deviation rate function for quantifying the likelihood of observing rare protein production rates and the corresponding driven process that characterizes the system dynamics conditional on the rare event) for models of post-transcriptional regulation directly from prior results for promoter-based models. The results derived create new avenues to analyze rare events in general models of post-transcriptional regulation pertaining to various different biological settings.

q-bio.QM