Leloup J C, Goldbeter A
Faculté des Sciences, Université Libre de Bruxelles, Campus Plaine, Brussels, Belgium.
Bioessays. 2000 Jan;22(1):84-93. doi: 10.1002/(SICI)1521-1878(200001)22:1<84::AID-BIES13>3.0.CO;2-I.
Thanks to genetic and biochemical advances on the molecular mechanism of circadian rhythms in Drosophila, theoretical models closely related to experimental observations can be considered for the regulatory mechanism of the circadian clock in this organism. Modeling is based on the autoregulatory negative feedback exerted by a complex between PER and TIM proteins on the expression of per and tim genes. The model predicts the occurrence of sustained circadian oscillations in continuous darkness. When incorporating light-induced TIM degradation, the model accounts for damping of oscillations in constant light, entrainment of the rhythm by light-dark cycles of varying period or photoperiod, and phase shifting by light pulses. The model further provides a molecular dynamical explanation for the permanent or transient suppression of circadian rhythmicity triggered in a variety of organisms by a critical pulse of light. Finally, the model shows that to produce a robust rhythm the various clock genes must be expressed at the appropriate levels since sustained oscillations only occur in a precise range of parameter values. BioEssays 22:84-93, 2000.
得益于果蝇昼夜节律分子机制方面的遗传学和生物化学进展,对于该生物体昼夜节律钟的调节机制,可以考虑与实验观察结果密切相关的理论模型。建模基于PER和TIM蛋白之间的复合物对per和tim基因表达施加的自动调节负反馈。该模型预测在持续黑暗中会出现持续的昼夜节律振荡。当纳入光诱导的TIM降解时,该模型解释了在恒定光照下振荡的衰减、不同周期或光周期的明暗循环对节律的同步以及光脉冲引起的相位偏移。该模型还为各种生物体中由临界光脉冲触发的昼夜节律性的永久或短暂抑制提供了分子动力学解释。最后,该模型表明,要产生稳健的节律,各种时钟基因必须在适当水平表达,因为持续振荡仅在精确的参数值范围内发生。《生物论文》22:84 - 93,2000年。