CNRS, CRN2M-UMR7286, Faculté de Médecine Nord, Aix-Marseille Université, Marseille, France.
Wiley Interdiscip Rev RNA. 2018 May;9(3):e1467. doi: 10.1002/wrna.1467. Epub 2018 Feb 9.
The circadian clock drives daily rhythms of multiple physiological processes, allowing organisms to anticipate and adjust to periodic changes in environmental conditions. These physiological rhythms are associated with robust oscillations in the expression of at least 30% of expressed genes. While the ability for the endogenous timekeeping system to generate a 24-hr cycle is a cell-autonomous mechanism based on negative autoregulatory feedback loops of transcription and translation involving core-clock genes and their protein products, it is now increasingly evident that additional mechanisms also govern the circadian oscillations of clock-controlled genes. Such mechanisms can take place post-transcriptionally during the course of the RNA life cycle. It has been shown that many steps during RNA processing are regulated in a circadian manner, thus contributing to circadian gene expression. These steps include mRNA capping, alternative splicing, changes in splicing efficiency, and changes in RNA stability controlled by the tail length of polyadenylation or the use of alternative polyadenylation sites. RNA transport can also follow a circadian pattern, with a circadian nuclear retention driven by rhythmic expression within the nucleus of particular bodies (the paraspeckles) and circadian export to the cytoplasm driven by rhythmic proteins acting like cargo. Finally, RNA degradation may also follow a circadian pattern through the rhythmic involvement of miRNAs. In this review, we summarize the current knowledge of the post-transcriptional circadian mechanisms known to play a prominent role in shaping circadian gene expression in mammals. This article is categorized under: RNA Processing > Splicing Regulation/Alternative Splicing RNA Processing > RNA Editing and Modification RNA Export and Localization > Nuclear Export/Import.
生物钟驱动着多种生理过程的日常节律,使生物体能够预测和适应环境条件的周期性变化。这些生理节律与至少 30%表达基因的表达强震荡相关。虽然内源性计时系统产生 24 小时周期的能力是一种基于转录和翻译的核心时钟基因及其蛋白产物的负反馈自动调节的细胞自主机制,但现在越来越明显的是,其他机制也控制着时钟控制基因的昼夜节律震荡。这种机制可以在 RNA 生命周期的过程中发生在转录后。已经表明,在 RNA 处理的许多步骤中,昼夜节律调节发生,从而有助于昼夜节律基因表达。这些步骤包括 mRNA 加帽、选择性剪接、剪接效率的变化,以及由多聚腺苷酸化的尾部长度或使用替代多聚腺苷酸化位点控制的 RNA 稳定性变化。RNA 转运也可以遵循昼夜节律模式,由核内特定体(核斑)内的节律性表达驱动的昼夜核保留和由类似货物的节律性蛋白驱动的昼夜细胞质输出。最后,通过 miRNA 的周期性参与,RNA 降解也可能遵循昼夜节律模式。在这篇综述中,我们总结了目前已知的在哺乳动物中塑造昼夜节律基因表达中起重要作用的转录后昼夜机制的知识。本文属于以下类别:RNA 加工 > 剪接调控/选择性剪接 RNA 加工 > RNA 编辑和修饰 RNA 输出和定位 > 核输出/导入。