Department of Chemistry, Physics and Applied Mathematics, State University of New York at Stony Brook, Stony Brook, New York, USA.
Biophys J. 2012 Mar 7;102(5):1001-10. doi: 10.1016/j.bpj.2012.02.002. Epub 2012 Mar 6.
We quantify the potential landscape to determine the global stability and coherence of biological oscillations. We explore a gene network motif in our experimental synthetic biology studies of two genes that mutually repress and activate each other with self-activation and self-repression. We find that in addition to intrinsic molecular number fluctuations, there is another type of fluctuation crucial for biological function: the fluctuation due to the slow binding/unbinding of protein regulators to gene promoters. We find that coherent limit cycle oscillations emerge in two regimes: an adiabatic regime with fast binding/unbinding and a nonadiabatic regime with slow binding/unbinding relative to protein synthesis/degradation. This leads to two mechanisms of producing the stable oscillations: the effective interactions from averaging the gene states in the adiabatic regime; and the time delays due to slow binding/unbinding to promoters in the nonadiabatic regime, which can be tested by forthcoming experiments. In both regimes, the landscape has a topological shape of the Mexican hat in protein concentrations that quantitatively determines the global stability of limit cycle dynamics. The oscillation coherence is shown to be correlated with the shape of the Mexican hat characterized by the height from the oscillation ring to the central top. The oscillation period can be tuned in a wide range by changing the binding/unbinding rate without changing the amplitude much, which is important for the functionality of a biological clock. A negative feedback loop with time delays due to slow binding/unbinding can also generate oscillations. Although positive feedback is not necessary for generating oscillations, it can make the oscillations more robust.
我们量化了潜在的景观,以确定生物振荡的全局稳定性和相干性。我们在实验合成生物学研究中探索了一个基因网络基序,该基序涉及两个相互抑制和激活彼此的基因,具有自我激活和自我抑制作用。我们发现,除了内在的分子数量波动外,还有另一种波动对于生物功能至关重要:由于蛋白质调节剂与基因启动子的缓慢结合/解吸而引起的波动。我们发现,在两个区域中出现了相干的极限环振荡:结合/解吸速度快的绝热区和结合/解吸相对于蛋白质合成/降解较慢的非绝热区。这导致了产生稳定振荡的两种机制:在绝热区中平均基因状态的有效相互作用;以及在非绝热区中由于与启动子的缓慢结合/解吸而导致的时间延迟,可以通过即将进行的实验进行测试。在这两个区域中,景观在蛋白质浓度中具有墨西哥帽的拓扑形状,该形状定量地确定了极限环动力学的全局稳定性。显示出的振荡相干性与墨西哥帽的形状相关联,该形状由从振荡环到中央顶部的高度来表征。通过改变结合/解吸速率而不改变幅度,可以在很宽的范围内调整振荡周期,这对于生物钟的功能很重要。由于结合/解吸缓慢而导致的具有时间延迟的负反馈回路也可以产生振荡。尽管正反馈对于产生振荡不是必需的,但它可以使振荡更健壮。