Scheper T, Klinkenberg D, Pennartz C, van Pelt J
Oxford Brookes University, School for Computing and Math Science, Gipsy Lane Campus, OX3 0BP Headington Oxford, United Kingdom.
J Neurosci. 1999 Jan 1;19(1):40-7. doi: 10.1523/JNEUROSCI.19-01-00040.1999.
A mathematical model for the intracellular circadian rhythm generator has been studied, based on a negative feedback of protein products on the transcription rate of their genes. The study is an attempt at examining minimal but biologically realistic requirements for a negative molecular feedback loop involving considerably faster reactions, to produce (slow) circadian oscillations. The model included mRNA and protein production and degradation, along with a negative feedback of the proteins upon mRNA production. The protein production process was described solely by its total duration and a nonlinear term, whereas also the feedback included nonlinear interactions among protein molecules. This system was found to produce robust oscillations in protein and mRNA levels over a wide range of parameter values. Oscillations were slow, with periods much longer than the time constants of any of the individual system parameters. Circadian oscillations were obtained for realistic values of the parameters. The system was readily entrainable to external periodic perturbations. Two distinct classes of phase response curves were found, viz. with or without a time domain within the circadian cycle in which external perturbations fail to induce a phase shift ("dead zone"). The delay and nonlinearity in the protein production and the cooperativity in the negative feedback (Hill coefficient) were for this model found to be necessary and sufficient to generate robust circadian oscillations. The similarities between model outcomes and empirical findings establish that circadian rhythmicity at the cellular level can plausibly emerge from interactions among molecular systems which are not in themselves rhythmic.
基于蛋白质产物对其基因转录速率的负反馈,研究了一种细胞内昼夜节律发生器的数学模型。该研究旨在探讨一个涉及速度快得多的反应的负分子反馈回路产生(缓慢的)昼夜振荡所需的最小但符合生物学实际的条件。该模型包括mRNA和蛋白质的产生与降解,以及蛋白质对mRNA产生的负反馈。蛋白质产生过程仅由其总持续时间和一个非线性项来描述,而反馈中也包括蛋白质分子之间的非线性相互作用。研究发现,该系统在很宽的参数值范围内能产生蛋白质和mRNA水平的稳健振荡。振荡很缓慢,其周期比任何单个系统参数的时间常数长得多。对于符合实际的参数值,能获得昼夜振荡。该系统很容易被外部周期性扰动所同步。发现了两类不同的相位响应曲线,即昼夜周期内有或没有一个外部扰动无法诱导相位偏移的时域(“死区”)。对于该模型,发现蛋白质产生中的延迟和非线性以及负反馈中的协同性(希尔系数)对于产生稳健的昼夜振荡是必要且充分的。模型结果与实证发现之间的相似性表明,细胞水平上的昼夜节律可能合理地源于本身并无节律的分子系统之间的相互作用。