基于多尺度动力学的合成基因网络振荡子设计

Luonan Chen, Tetsuya J. Kobayashi, K. Aihara
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引用次数: 0

摘要

多稳定性、振荡和开关存在于生物过程和组织的各个层面,并在许多理论模型的基础上进行了研究,例如果蝇周期蛋白(PER)和永恒蛋白(TIM)的昼夜节律振荡,以及转录因子调节的多稳定性动力学。大量的实验证据表明,细胞过程本质上是有节奏的或周期性的。实验还观察到各种不同时间尺度的周期振荡,从不到一秒到一年多不等,这可能使生物体能够适应周期性变化的环境。另一方面,在合成基因网络中,拨动开关和再调节器都已从理论上提出并得到实验的进一步证实。所有这些工作都强调了转录因子反馈调节的重要性,这是引起生物遗传系统所表现出的振荡或多稳态动力学行为的关键。此外,应该指出的是,许多周期行为不是简单地平滑振荡;相反,它们会迅速变化或在某些状态下跳跃。在基因表达系统中,许多不同的时间尺度表征了基因调控过程。例如,转录和翻译过程通常在比磷酸化、二聚化或转录因子结合反应慢得多的时间尺度上进化。在遗传网络中,一些基因的表达时间比其他基因慢得多,这取决于基因的长度。我们的目标是通过简单的非线性模型设计合成基因-蛋白质系统中的鲁棒周期振子,并利用多时间尺度性质分析具有跳跃行为或松弛振荡的极限环的基本机制[1,2]。研究表明,周期振荡主要由基因调控系统中的非线性反馈回路和生化反应间时间尺度差异引起的跳跃动力学产生。此外,还研究了时间延迟的影响。我们表明,时滞通常会扩大振荡的稳定区域,从而使振荡在参数变化或噪声的情况下更具可持续性[1,2]。所提出的模型在参数扰动或环境变化的稳定性和周期长度方面具有鲁棒性。虽然我们主要分析一些特定的模型,但在这项工作中确定的机制可能适用于各种遗传调控系统。这些简单的模型实际上可以作为合成基因-蛋白质网络的基本构建块,例如遗传振荡器或开关,因为动态对参数扰动或环境变化具有鲁棒性。还提供了几个例子来演示利用/spl λ /噬菌体细菌的基因实现合成振荡器。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Designing oscillators in synthetic gene networks based on multi-scale dynamics
Multistability, oscillations, and switching exist at various levels of biological processes and organizations and have been investigated on the basis of many theoretical models, such as circadian oscillations with the period protein (PER) and the timeless protein (TIM) in Drosophila, and multistable dynamics regulated by transcriptional factors. Considerable experimental evidence suggests that cellular processes are intrinsically rhythmic or periodic. Various periodic oscillations with different time scales ranging from less than a second to more than a year, which may allow for living organisms to adapt their behaviors to a periodically varying environment, have also been observed experimentally. On the other hand, in synthetic gene networks, both toggle switch and repressilator have been theoretically proposed and further confirmed by experiments. All of these works stress the importance of feedback regulation of transcriptional factors, which is a key in giving rise to oscillatory or multistable dynamical behaviors exhibited by biological genetic systems. In addition, it should be noted that many periodic behaviors do not simply oscillate smoothly; rather, they change rapidly or jump at certain states. In gene expression systems, many different time scales characterize the gene regulatory processes. For instance, the transcription and translation processes generally evolve on a time scale that is much slower than that of phosphorylation, dimerization or binding reactions of transcription factors. In genetic networks, the time scale for expression of some genes is much slower than that of others, depending on the length of the genes. We aim to design robust periodic oscillators in synthetic gene-protein systems by simple nonlinear models and to analyze the basic mechanism of limit cycles with jumping behaviors or relaxation oscillations by exploiting multiple time-scale properties [1, 2]. We show that periodic oscillations are mainly generated by nonlinear feedback loops in gene regulatory systems and the jumping dynamics caused by time scale differences among biochemical reactions. Moreover, effects of time delay are also examined. We show that time delay generally enlarges the stability region of oscillations, thereby making the oscillations more sustainable despite parameter changes or noise [1, 2]. The dynamics of the proposed models is robust in terms of stability and period length to the parameter perturbations or environment variations. Although we mainly analyze some specific models, the mechanisms identified in this work are likely to apply to a variety of genetic regulatory systems. These simple models may actually act as basic building block in synthetic gene-protein networks, such as genetic oscillators or switches because the dynamics is robust for parameter perturbations or environment variations. Several examples are also provided to demonstrate implementation of synthetic oscillators by using genes of the /spl lambda/ phage bacteria.
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