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crm 基因的一个等位基因阻断了蓝藻的生物钟节律。

An allele of the crm gene blocks cyanobacterial circadian rhythms.

机构信息

Center for Chronobiology, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.

出版信息

Proc Natl Acad Sci U S A. 2013 Aug 20;110(34):13950-5. doi: 10.1073/pnas.1312793110. Epub 2013 Aug 5.

Abstract

The SasA-RpaA two-component system constitutes a key output pathway of the cyanobacterial Kai circadian oscillator. To date, rhythm of phycobilisome associated (rpaA) is the only gene other than kaiA, kaiB, and kaiC, which encode the oscillator itself, whose mutation causes completely arrhythmic gene expression. Here we report a unique transposon insertion allele in a small ORF located immediately upstream of rpaA in Synechococcus elongatus PCC 7942 termed crm (for circadian rhythmicity modulator), which results in arrhythmic promoter activity but does not affect steady-state levels of RpaA. The crm ORF complements the defect when expressed in trans, but only if it can be translated, suggesting that crm encodes a small protein. The crm1 insertion allele phenotypes are distinct from those of an rpaA null; crm1 mutants are able to grow in a light:dark cycle and have no detectable oscillations of KaiC phosphorylation, whereas low-amplitude KaiC phosphorylation rhythms persist in the absence of RpaA. Levels of phosphorylated RpaA in vivo measured over time are significantly altered compared with WT in the crm1 mutant as well as in the absence of KaiC. Taken together, these results are consistent with the hypothesis that the Crm polypeptide modulates a circadian-specific activity of RpaA.

摘要

SasA-RpaA 双组分系统构成了蓝藻 Kai 生物钟振荡器的关键输出途径。迄今为止,藻胆体相关(rpaA)的节律是除 kaiA、kaiB 和 kaiC 之外唯一的基因,这些基因编码振荡器本身,其突变导致完全无节律的基因表达。在这里,我们报告了一种在 Synechococcus elongatus PCC 7942 中 rpaA 上游紧邻的一个小 ORF 中发现的独特转座子插入等位基因,称为 crm(circadian rhythmicity modulator,生物钟节律调节剂),它导致启动子活性无节律,但不影响 RpaA 的稳态水平。crm ORF 在反式表达时可以互补缺陷,但只有在能够翻译的情况下才可以,这表明 crm 编码一种小蛋白。crm1 插入等位基因的表型与 rpaA 缺失的表型不同;crm1 突变体能够在光暗循环中生长,并且 KaiC 磷酸化没有可检测到的振荡,而在没有 RpaA 的情况下,低幅度的 KaiC 磷酸化节律仍然存在。与 WT 相比,crm1 突变体以及在没有 KaiC 的情况下,体内测量的磷酸化 RpaA 水平随时间的变化显著改变。这些结果与假设一致,即 Crm 多肽调节 RpaA 的生物钟特异性活性。

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