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labA: a novel gene required for negative feedback regulation of the cyanobacterial circadian clock protein KaiC.实验室A:一种蓝藻生物钟蛋白KaiC负反馈调节所需的新基因。
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本文引用的文献

1
Cyanobacterial daily life with Kai-based circadian and diurnal genome-wide transcriptional control in Synechococcus elongatus.集胞藻中基于Kai的昼夜节律和全基因组转录调控的蓝藻日常生活。
Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):14168-73. doi: 10.1073/pnas.0902587106. Epub 2009 Jul 30.
2
Dual KaiC-based oscillations constitute the circadian system of cyanobacteria.基于双 KaiC 的振荡构成了蓝藻的昼夜节律系统。
Genes Dev. 2008 Jun 1;22(11):1513-21. doi: 10.1101/gad.1661808. Epub 2008 May 13.
3
A sequential program of dual phosphorylation of KaiC as a basis for circadian rhythm in cyanobacteria.作为蓝藻生物钟基础的KaiC双磷酸化顺序程序。
EMBO J. 2007 Sep 5;26(17):4029-37. doi: 10.1038/sj.emboj.7601832. Epub 2007 Aug 23.
4
labA: a novel gene required for negative feedback regulation of the cyanobacterial circadian clock protein KaiC.实验室A:一种蓝藻生物钟蛋白KaiC负反馈调节所需的新基因。
Genes Dev. 2007 Jan 1;21(1):60-70. doi: 10.1101/gad.1488107.
5
Quinone sensing by the circadian input kinase of the cyanobacterial circadian clock.蓝藻生物钟的昼夜节律输入激酶对醌的感应
Proc Natl Acad Sci U S A. 2006 Nov 14;103(46):17468-73. doi: 10.1073/pnas.0606639103. Epub 2006 Nov 6.
6
A KaiC-associating SasA-RpaA two-component regulatory system as a major circadian timing mediator in cyanobacteria.一种与 KaiC 相关联的 SasA-RpaA 双组分调节系统,作为蓝细菌中的主要昼夜节律计时介质。
Proc Natl Acad Sci U S A. 2006 Aug 8;103(32):12109-14. doi: 10.1073/pnas.0602955103. Epub 2006 Aug 1.
7
Cyanobacterial circadian pacemaker: Kai protein complex dynamics in the KaiC phosphorylation cycle in vitro.蓝藻生物钟起搏器:体外KaiC磷酸化循环中Kai蛋白复合体的动力学
Mol Cell. 2006 Jul 21;23(2):161-71. doi: 10.1016/j.molcel.2006.05.039.
8
The pseudo-receiver domain of CikA regulates the cyanobacterial circadian input pathway.CikA的伪受体结构域调控蓝藻生物钟输入途径。
Mol Microbiol. 2006 May;60(3):658-68. doi: 10.1111/j.1365-2958.2006.05138.x.
9
Reconstitution of circadian oscillation of cyanobacterial KaiC phosphorylation in vitro.体外重建蓝藻生物钟蛋白KaiC磷酸化的昼夜节律振荡
Science. 2005 Apr 15;308(5720):414-5. doi: 10.1126/science.1108451.
10
LdpA: a component of the circadian clock senses redox state of the cell.LdpA:生物钟的一个组成部分,可感知细胞的氧化还原状态。
EMBO J. 2005 Mar 23;24(6):1202-10. doi: 10.1038/sj.emboj.7600606. Epub 2005 Mar 10.

基于 KaiABC 的振荡器的三个主要输出途径协同作用,以在蓝藻中产生稳健的生物钟 kaiBC 表达。

Three major output pathways from the KaiABC-based oscillator cooperate to generate robust circadian kaiBC expression in cyanobacteria.

机构信息

Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan.

出版信息

Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):3263-8. doi: 10.1073/pnas.0909924107. Epub 2010 Jan 28.

DOI:10.1073/pnas.0909924107
PMID:20133618
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2840301/
Abstract

Circadian kaiBC expression in the cyanobacterium Synechococcus elongatus PCC 7942 is generated by temporal information transmission from the KaiABC-based circadian oscillator to RpaA, a putative transcriptional factor, via the SasA-dependent positive pathway and the LabA-dependent negative pathway which is responsible for feedback regulation of KaiC. However, the labA/sasA double mutant has a circadian kaiBC expression rhythm, suggesting that there is an additional circadian output pathway. Here we describe a third circadian output pathway, which is CikA-dependent. The cikA mutation attenuates KaiC overexpression-induced kaiBC repression and exacerbates the low-amplitude phenotype of the labA mutant, suggesting that cikA acts as a negative regulator of kaiBC expression independent of the LabA-dependent pathway. In the labA/sasA/cikA triple mutant, kaiBC promoter activity becomes almost arrhythmic, despite preservation of the circadian KaiC phosphorylation rhythm, suggesting that CikA largely accounts for the residual kaiBC expression rhythm observed in the labA/sasA double mutant. These results also strongly suggest that transcriptional regulation in the labA/sasA/cikA triple mutant is insulated from the circadian signals of the KaiABC-based oscillator. Based on these observations, we propose a model in which temporal information from the KaiABC-based circadian oscillator is transmitted to gene expression through three separate output pathways.

摘要

生物钟 KaiBC 在蓝藻 Synechococcus elongatus PCC 7942 中的表达是由基于 KaiABC 的生物钟振荡器通过 SasA 依赖的正调控途径和 LabA 依赖的负调控途径向假定的转录因子 RpaA 传递时间信息而产生的,该负调控途径负责 KaiC 的反馈调节。然而,labA/sasA 双突变体具有生物钟 KaiBC 表达节律,这表明存在额外的生物钟输出途径。在这里,我们描述了第三个生物钟输出途径,该途径依赖于 CikA。cikA 突变削弱了 KaiC 过表达诱导的 kaiBC 抑制作用,并加剧了 labA 突变体的低振幅表型,这表明 cikA 作为 kaiBC 表达的负调节剂独立于 LabA 依赖途径发挥作用。在 labA/sasA/cikA 三重突变体中,kaiBC 启动子活性几乎变得无节律,尽管 KaiC 的生物钟磷酸化节律得以保留,这表明 CikA 在很大程度上解释了在 labA/sasA 双突变体中观察到的残留 kaiBC 表达节律。这些结果还强烈表明,labA/sasA/cikA 三重突变体中的转录调控与基于 KaiABC 的生物钟振荡器的生物钟信号隔离开来。基于这些观察结果,我们提出了一个模型,其中基于 KaiABC 的生物钟振荡器的时间信息通过三个独立的输出途径传递到基因表达。