Department of Physics, University of Illinois at Urbana-Champaign, Urbana, Illinois; Carl Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, Illinois.
Carl Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, Illinois; Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois.
Biophys J. 2018 Feb 6;114(3):737-746. doi: 10.1016/j.bpj.2017.12.010.
Quantitative modeling of gene circuits is fundamentally important to synthetic biology, as it offers the potential to transform circuit engineering from trial-and-error construction to rational design and, hence, facilitates the advance of the field. Currently, typical models regard gene circuits as isolated entities and focus only on the biochemical processes within the circuits. However, such a standard paradigm is getting challenged by increasing experimental evidence suggesting that circuits and their host are intimately connected, and their interactions can potentially impact circuit behaviors. Here we systematically examined the roles of circuit-host coupling in shaping circuit dynamics by using a self-activating gene switch as a model circuit. Through a combination of deterministic modeling, stochastic simulation, and Fokker-Planck equation formalism, we found that circuit-host coupling alters switch behaviors across multiple scales. At the single-cell level, it slows the switch dynamics in the high protein production regime and enlarges the difference between stable steady-state values. At the population level, it favors cells with low protein production through differential growth amplification. Together, the two-level coupling effects induce both quantitative and qualitative modulations of the switch, with the primary component of the effects determined by the circuit's architectural parameters. This study illustrates the complexity and importance of circuit-host coupling in modulating circuit behaviors, demonstrating the need for a new paradigm-integrated modeling of the circuit-host system-for quantitative understanding of engineered gene networks.
基因回路的定量建模对于合成生物学至关重要,因为它有可能将电路工程从反复试验的构建转变为合理的设计,从而推动该领域的发展。目前,典型的模型将基因电路视为孤立的实体,仅关注电路内的生化过程。然而,越来越多的实验证据表明,这种标准范式正受到挑战,电路及其宿主之间存在密切联系,它们的相互作用可能会影响电路的行为。在这里,我们使用自激活基因开关作为模型电路,系统地研究了电路-宿主耦合在塑造电路动力学中的作用。通过确定性建模、随机模拟和福克-普朗克方程形式主义的结合,我们发现电路-宿主耦合在多个尺度上改变了开关的行为。在单细胞水平上,它在高蛋白质产生的情况下减缓了开关动力学,并扩大了稳定稳态值之间的差异。在群体水平上,它通过差异生长放大有利于蛋白质产量低的细胞。总之,两级耦合效应引起了开关的定量和定性调节,效应的主要组成部分由电路的结构参数决定。这项研究说明了电路-宿主耦合在调节电路行为方面的复杂性和重要性,表明需要对电路-宿主系统进行新的综合建模,以实现对工程基因网络的定量理解。