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全面建模神经节孢生物钟及其温度补偿。

Comprehensive modelling of the Neurospora circadian clock and its temperature compensation.

机构信息

University of Manchester, Manchester, United Kingdom.

出版信息

PLoS Comput Biol. 2012;8(3):e1002437. doi: 10.1371/journal.pcbi.1002437. Epub 2012 Mar 29.

Abstract

Circadian clocks provide an internal measure of external time allowing organisms to anticipate and exploit predictable daily changes in the environment. Rhythms driven by circadian clocks have a temperature compensated periodicity of approximately 24 hours that persists in constant conditions and can be reset by environmental time cues. Computational modelling has aided our understanding of the molecular mechanisms of circadian clocks, nevertheless it remains a major challenge to integrate the large number of clock components and their interactions into a single, comprehensive model that is able to account for the full breadth of clock phenotypes. Here we present a comprehensive dynamic model of the Neurospora crassa circadian clock that incorporates its key components and their transcriptional and post-transcriptional regulation. The model accounts for a wide range of clock characteristics including: a periodicity of 21.6 hours, persistent oscillation in constant conditions, arrhythmicity in constant light, resetting by brief light pulses, and entrainment to full photoperiods. Crucial components influencing the period and amplitude of oscillations were identified by control analysis. Furthermore, simulations enabled us to propose a mechanism for temperature compensation, which is achieved by simultaneously increasing the translation of frq RNA and decreasing the nuclear import of FRQ protein.

摘要

生物钟为生物体提供了一种内部的外部时间度量方式,使它们能够预测和利用环境中可预测的日常变化。由生物钟驱动的节律具有约 24 小时的温度补偿周期性,在恒定条件下持续存在,并可以通过环境时间线索进行重置。计算建模有助于我们理解生物钟的分子机制,但将大量的时钟组件及其相互作用整合到一个能够解释完整时钟表型的单一、综合模型仍然是一个主要挑战。在这里,我们提出了一个Neurospora crassa 生物钟的综合动态模型,该模型包含了其关键组件及其转录和转录后调控。该模型解释了广泛的时钟特征,包括:周期为 21.6 小时,在恒定条件下持续振荡,在恒定光照下无节律,短光脉冲重置,以及对全光周期的驯化。通过控制分析确定了影响振荡周期和幅度的关键组件。此外,模拟使我们能够提出一种温度补偿机制,该机制通过同时增加 frq RNA 的翻译和减少 FRQ 蛋白的核内输入来实现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0172/3320131/80acea99d39a/pcbi.1002437.g001.jpg

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