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In the Driver's Seat: The Case for Transcriptional Regulation and Coupling as Relevant Determinants of the Circadian Transcriptome and Proteome in Eukaryotes

机译:在驾驶席上:转录调控和耦合作为真核生物昼夜转录组和蛋白质组相关决定因素的案例

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Circadian clocks drive daily oscillations in a variety of biological processes through the coordinate orchestration of precise gene expression programs. Global expression profiling experiments have suggested that a significant fraction of the transcriptome and proteome is under circadian control, and such output rhythms have historically been assumed to rely on the rhythmic transcription of these genes. Recent genome-wide studies, however, have challenged this long-held view and pointed to a major contribution of posttranscriptional regulation in driving oscillations at the messenger RNA (mRNA) level, while others have highlighted extensive clock translational regulation, regardless of mRNA rhythms. There are various examples of genes that are uniformly transcribed throughout the day but that exhibit rhythmic mRNA levels, and of flat mRNAs, with oscillating protein levels, and such observations have largely been considered to result from independent regulation at each step. These studies have thereby obviated any connections, or coupling, that might exist between the different steps of gene expression and the impact that any of them could have on subsequent ones. Here, we argue that due to both biological and technical reasons, the jury is still out on the determination of the relative contributions of each of the different stages of gene expression in regulating output molecular rhythms. In addition, we propose that through a variety of coupling mechanisms, gene transcription (even when apparently arrhythmic) might play a much relevant role in determining oscillations in gene expression than currently estimated, regulating rhythms at downstream steps. Furthermore, we posit that eukaryotic genomes regulate daily RNA polymerase II (RNAPII) recruitment and histone modifications genome-wide, setting the stage for global nascent transcription, but that tissue-specific mechanisms locally specify the different processes under clock control.
机译:昼夜节律时钟通过精确的基因表达程序的协调编排来驱动各种生物学过程中的日常振荡。全局表达谱分析实验表明,转录组和蛋白质组中有很大一部分处于昼夜节律的控制之下,并且这种输出节律在历史上一直被认为依赖于这些基因的节律性转录。然而,最近的全基因组研究挑战了这一长期存在的观点,并指出转录后调控在驱动信使RNA(mRNA)级别的振荡方面的重要贡献,而其他研究则强调了广泛的时钟翻译调控,而与mRNA节律无关。有各种各样的基因实例全天均匀转录,但表现出节律性的mRNA水平,而扁平的mRNA具有振荡的蛋白质水平,这些观察结果在很大程度上被认为是每个步骤的独立调节所致。这些研究因此消除了基因表达的不同步骤之间可能存在的任何联系或耦合,以及它们中的任何一个对后续步骤的影响。在这里,我们认为,由于生物学和技术原因,陪审团仍未确定基因表达的每个不同阶段在调节输出分子节律中的相对作用。此外,我们提出,通过多种偶联机制,基因转录(即使明显存在心律不齐)在确定基因表达的振荡方面可能比目前估计的起重要作用,调节下游步骤的节律。此外,我们认为,真核基因组在全基因组范围内调节每日RNA聚合酶II(RNAPII)募集和组蛋白修饰,为全球新生转录奠定了基础,但是组织特异性机制局部指定了时钟控制下的不同过程。

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