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Circadian Yin-Yang Regulation and Its Manipulation to Globally Reprogram Gene Expression

机译:昼夜节律性阴阳调控及其操纵基因的全球重编程。

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Background: The cyanobacterial circadian program exerts genome-wide control of gene expression. KaiC undergoes rhythms of phosphorylation that are regulated by interactions with KaiA and KaiB. The phosphorylation status of KaiC is thought to mediate global transcription via output factors SasA, CikA, LabA, RpaA, and RpaB. Overexpression of kaiC has been reported to globally repress gene expression. Results: Here, we show that the positive circadian component KaiA upregulates "subjective dusk" genes and that its overexpression deactivates rhythmic gene expression without significantly affecting growth rates in constant light. We analyze the global patterns of expression that are regulated by KaiA versus KaiC and find in contrast to the previous report of KaiC repression that there is a "yin-yang" regulation of gene expression whereby kaiA overexpression activates "dusk genes" and represses "dawn genes," whereas kaiC overexpression complementarily activates dawn genes and represses dusk genes. Moreover, continuous induction of kaiA latched KaiABC-regulated gene expression to provide constitutively increased transcript levels of diverse endogenous and heterologous genes that are expressed in the predominant subjective dusk phase. In addition to analyzing KaiA regulation of endogenous gene expression, we apply these insights to the expression of heterologous proteins whose products are of potential value, namely human proinsulin, foreign luciferase, and exogenous hydrogenase. Conclusions: Both KaiC and KaiA complementarily contribute to the regulation of circadian gene expression via yin-yang switching. Circadian patterns can be reprogrammed by overexpression of kaiA or kaiC to constitutively enhance gene expression, and this reprogramming can improve 24/7 production of heterologous proteins that are useful as pharmaceuticals or biofuels.
机译:背景:蓝藻生物节律程序对基因表达进行全基因组控制。 KaiC经历的磷酸化节奏受与KaiA和KaiB相互作用的调节。认为KaiC的磷酸化状态可通过输出因子SasA,CikA,LabA,RpaA和RpaB介导全局转录。据报道,kaiC的过度表达可全面抑制基因表达。结果:在这里,我们表明正的昼夜节律成分KaiA上调“主观黄昏”基因,并且它的过度表达使节律性基因表达失活,而不会在恒定光照下显着影响生长速率。我们分析了KaiA与KaiC调控的全球表达模式,发现与KaiC压制的先前报告相反,基因表达存在“阴阳”调节,其中kaiA过表达激活“黄昏基因”并抑制“黎明”基因”,而kaiC过度表达会互补激活黎明基因并抑制黄昏基因。此外,持续诱导kaiA可以锁存KaiABC调节的基因表达,以提供在主观主观黄昏阶段表达的各种内源和异源基因的组成水平提高的转录水平。除了分析KaiA对内源基因表达的调控外,我们还将这些见解应用于其产物具有潜在价值的异源蛋白的表达,即人胰岛素原,外源荧光素酶和外源氢化酶。结论:KaiC和KaiA都通过阴阳转换互补地调节昼夜节律基因的表达。昼夜节律模式可以通过kaiA或kaiC的过表达来重新编程,从而组成性地增强基因表达,这种重新编程可以提高用作药物或生物燃料的异源蛋白的24/7产生。

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