A Statistical Approach Reveals Designs for the Most Robust Stochastic Gene Oscillators

被引:38
作者
Woods, Mae L. [1 ]
Leon, Miriam [1 ]
Perez-Carrasco, Ruben [2 ]
Barnes, Chris P. [1 ,3 ]
机构
[1] UCL, Dept Cell & Dev Biol, London WC1E 6BT, England
[2] UCL, Dept Math, London WC1E 6BT, England
[3] UCL, Dept Genet Evolut & Environm, London WC1E 6BT, England
基金
英国惠康基金;
关键词
oscillations; robustness; circuit topology; stochastic processes; sequential Monte Carlo; PROTEIN-DEGRADATION; MODEL SELECTION; BAYESIAN DESIGN; NETWORK MOTIFS; TOGGLE SWITCH; SYSTEMS; POPULATION; EXPRESSION; PRINCIPLES; EVOLUTION;
D O I
10.1021/acssynbio.5b00179
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:459 / 470
页数:12
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