Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan.
Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):3263-8. doi: 10.1073/pnas.0909924107. Epub 2010 Jan 28.
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.
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。