Goldbeter A
Faculté des Sciences, Université Libre de Bruxelles, Brussels, Belgium.
Proc Biol Sci. 1995 Sep 22;261(1362):319-24. doi: 10.1098/rspb.1995.0153.
The mechanism of circadian oscillations in the period protein (PER) in Drosophila is investigated by means of a theoretical model. Taking into account recent experimental observations, the model for the circadian clock is based on multiple phosphorylation of PER and on the negative feedback exerted by PER on the transcription of the period (per) gene. This minimal biochemical model provides a molecular basis for circadian oscillations of the limit cycle type. During oscillations, the peak in per mRNA precedes by several hours the peak in total PER protein. The results support the view that multiple PER phosphorylation introduces times delays which strengthen the capability of negative feedback to produce oscillations. The analysis shows that the rhythm only occurs in a range bounded by two critical values of the maximum rate of PER degradation. A similar result is obtained with respect to the rate of PER transport into the nucleus. The results suggest a tentative explanation for the altered period of per mutants, in terms of variations in the rate of PER degradation.
通过一个理论模型研究了果蝇周期蛋白(PER)昼夜节律振荡的机制。考虑到最近的实验观察结果,昼夜节律时钟模型基于PER的多重磷酸化以及PER对周期(per)基因转录施加的负反馈。这个最小生化模型为极限环类型的昼夜节律振荡提供了分子基础。在振荡过程中,per mRNA的峰值比总PER蛋白的峰值提前数小时出现。结果支持这样一种观点,即PER的多重磷酸化引入了时间延迟,从而增强了负反馈产生振荡的能力。分析表明,节律仅在由PER降解最大速率的两个临界值界定的范围内出现。关于PER转运到细胞核的速率也得到了类似结果。这些结果就PER降解速率的变化对per突变体周期改变提出了一个初步解释。