Pigolotti Simone, Krishna Sandeep, Jensen Mogens H
Instituto Mediterráneo de Estudios Avanzados IMEDEA (Consejo Superior de Investigaciones Cientificas-Universitat de les Illes Balears), Campus de la Universitat de les Illes Balears, E-07122 Palma de Mallorca, Spain.
Proc Natl Acad Sci U S A. 2007 Apr 17;104(16):6533-7. doi: 10.1073/pnas.0610759104. Epub 2007 Apr 5.
Organisms are equipped with regulatory systems that display a variety of dynamical behavior ranging from simple stable steady states, to switching and multistability, to oscillations. Earlier work has shown that oscillations in protein concentrations or gene expression levels are related to the presence of at least one negative feedback loop in the regulatory network. Here, we study the dynamics of a very general class of negative feedback loops. Our main result is that, when a single negative feedback loop dominates the dynamical behavior, the sequence of maxima and minima of the concentrations exhibit a pattern that uniquely identifies the interactions of the loop. This allows us to devise an algorithm to (i) test whether observed oscillating time series are consistent with a single underlying negative feedback loop, and if so, (ii) reconstruct the precise structure of the loop, i.e., the activating/repressing nature of each interaction. This method applies even when some variables are missing from the data set, or if the time series shows transients, like damped oscillations. We illustrate the relevance and the limits of validity of our method with three examples: p53-Mdm2 oscillations, circadian gene expression in cyanobacteria, and cyclic binding of cofactors at the estrogen-sensitive pS2 promoter.
生物体配备有调节系统,这些系统表现出从简单稳定稳态到切换和多稳态再到振荡等各种动态行为。早期的研究表明,蛋白质浓度或基因表达水平的振荡与调节网络中至少一个负反馈回路的存在有关。在此,我们研究一类非常普遍的负反馈回路的动力学。我们的主要结果是,当单个负反馈回路主导动态行为时,浓度的最大值和最小值序列呈现出一种模式,该模式唯一地确定了回路的相互作用。这使我们能够设计一种算法来:(i)测试观察到的振荡时间序列是否与单个潜在的负反馈回路一致,如果是,则(ii)重建回路的精确结构,即每种相互作用的激活/抑制性质。即使数据集中缺少一些变量,或者时间序列显示出瞬态,如阻尼振荡,该方法也适用。我们用三个例子说明了我们方法的相关性和有效性限制:p53-Mdm2振荡、蓝藻中的昼夜节律基因表达以及雌激素敏感的pS2启动子处辅因子的循环结合。