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Rethinking Transcriptional Activation in the Arabidopsis Circadian Clock

机译:重新思考拟南芥生物钟中的转录激活。

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摘要

Circadian clocks are biological timekeepers that allow living cells to time their activity in anticipation of predictable daily changes in light and other environmental factors. The complexity of the circadian clock in higher plants makes it difficult to understand the role of individual genes or molecular interactions, and mathematical modelling has been useful in guiding clock research in model organisms such as Arabidopsis thaliana.We present a model of the circadian clock in Arabidopsis, based on a large corpus of published time course data. It appears from experimental evidence in the literature that most interactions in the clock are repressive. Hence, we remove all transcriptional activation found in previous models of this system, and instead extend the system by including two new components, the morning-expressed activator RVE8 and the nightly repressor/activator NOX.Our modelling results demonstrate that the clock does not need a large number of activators in order to reproduce the observed gene expression patterns. For example, the sequential expression of the PRR genes does not require the genes to be connected as a series of activators. In the presented model, transcriptional activation is exclusively the task of RVE8. Predictions of how strongly RVE8 affects its targets are found to agree with earlier interpretations of the experimental data, but generally we find that the many negative feedbacks in the system should discourage intuitive interpretations of mutant phenotypes. The dynamics of the clock are difficult to predict without mathematical modelling, and the clock is better viewed as a tangled web than as a series of loops.
机译:昼夜生物钟是生物计时器,可以使活细胞对活动进行计时,以预期光线和其他环境因素的每日可预测变化。高等植物中生物钟的复杂性使得难以理解单个基因或分子相互作用的作用,数学建模对于指导模式生物如拟南芥中的生物钟研究非常有用。拟南芥,基于大量已发布的时程数据。从文献中的实验证据看来,时钟中的大多数相互作用都是抑制性的。因此,我们删除了该系统先前模型中发现的所有转录激活,而是通过添加两个新组件来扩展系统,即早晨表达的激活剂RVE8和夜间阻遏物/激活剂NOX。我们的建模结果表明时钟不需要为了复制观察到的基因表达模式,需要大量激活剂。例如,PRR基因的顺序表达不需要将基因作为一系列激活子连接。在提出的模型中,转录激活仅是RVE8的任务。人们发现RVE8对靶标的强烈影响的预测与实验数据的早期解释是一致的,但通常我们发现系统中的许多负面反馈会阻碍对突变表型的直观解释。如果不进行数学建模,就很难预测时钟的动态性,并且最好将时钟看作是纠结的网络,而不是一系列的循环。

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