Abstract

The engineering of transcriptional networks presents many challenges due to the inherent uncertainty in the system structure, changing cellular context, and stochasticity in the governing dynamics. One approach to address these problems is to design and build systems that can function across a range of conditions; that is they are robust to uncertainty in their constituent components. Here we examine the parametric robustness landscape of transcriptional oscillators, which underlie many important processes such as circadian rhythms and the cell cycle, plus also serve as a model for the engineering of complex and emergent phenomena. The central questions that we address are: Can we build genetic oscillators that are more robust than those already constructed? Can we make genetic oscillators arbitrarily robust? These questions are technically challenging due to the large model and parameter spaces that must be efficiently explored. Here we use a measure of robustness that coincides with the Bayesian model evidence, combined with an efficient Monte Carlo method to traverse model space and concentrate on regions of high robustness, which enables the accurate evaluation of the relative robustness of gene network models governed by stochastic dynamics. We report the most robust two and three gene oscillator systems, plus examine how the number of interactions, the presence of autoregulation, and degradation of mRNA and protein affects the frequency, amplitude, and robustness of transcriptional oscillators. We also find that there is a limit to parametric robustness, beyond which there is nothing to be gained by adding additional feedback. Importantly, we provide predictions on new oscillator systems that can be constructed to verify the theory and advance design and modeling approaches to systems and synthetic biology.

Highlights

  • A major challenge facing the progress of synthetic biology is the design and implementation of systems that function in the face of fluctuating cellular environments

  • We found that only five models were capable of oscillations at the specified frequency (Materials and Methods), which we denote by M1−5

  • We have presented a mathematical framework for the modeling and analysis of robustness in stochastic biological systems and applied it to the case of stochastic transcriptional oscillators

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Summary

Introduction

A major challenge facing the progress of synthetic biology is the design and implementation of systems that function in the face of fluctuating cellular environments. To develop more predictable design and modeling frameworks that can calculate realistic estimates of system properties, including robustness, requires approaches that can handle a large number of parameters, parametric uncertainty, and stochastic dynamics. This can be achieved using sequential Monte Carlo methods.[40,41] Here we extend the Monte Carlo framework to include model space exploration.

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