Abstract

Recent advances in single-molecule fluorescent imaging have enabled quantitative measurements of transcription at a single gene copy, yet an accurate understanding of transcriptional kinetics is still lacking due to the difficulty of solving detailed biophysical models. Here we introduce a stochastic simulation and statistical inference platform for modeling detailed transcriptional kinetics in prokaryotic systems, which has not been solved analytically. The model includes stochastic two-state gene activation, mRNA synthesis initiation and stepwise elongation, release to the cytoplasm, and stepwise co-transcriptional degradation. Using the Gillespie algorithm, the platform simulates nascent and mature mRNA kinetics of a single gene copy and predicts fluorescent signals measurable by time-lapse single-cell mRNA imaging, for different experimental conditions. To approach the inverse problem of estimating the kinetic parameters of the model from experimental data, we develop a heuristic optimization method based on the genetic algorithm and the empirical distribution of mRNA generated by simulation. As a demonstration, we show that the optimization algorithm can successfully recover the transcriptional kinetics of simulated and experimental gene expression data. The platform is available as a MATLAB software package at https://data.caltech.edu/records/1287.

Highlights

  • Transcription has been the focus of intensive study due to its cornerstone role in cell activity regulation

  • We describe a new platform for simulating mRNA transcription and degradation on a submolecular level, available at https://data.caltech.edu/records/1287

  • Its output is directly comparable to single-cell data of nascent and mature mRNA

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Summary

Introduction

Transcription has been the focus of intensive study due to its cornerstone role in cell activity regulation. Recent advances in fluorescent imaging have enabled mRNA detection at singlemolecule resolution in individual cells, in both live and fixed samples [1,2]. Spatial analysis of mRNA signals allows the identification [3,4] and quantification [5] of nascent (actively transcribed) mRNA, which offers a direct window into the kinetics of gene transcription, with minimal interference from downstream effects [5], at the level of a single gene copy [6]. Converting high-resolution experimental data into theoretical understanding of transcription requires simultaneous modeling of both nascent and mature species of mRNA.

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