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RcsB-BglJ-mediated activation of Cascade operon does not induce the maturation of CRISPR RNAs in E. coli K12

机译:RcsB-BglJ介导的Cascade操纵子激活不会诱导E.coli K12中CRISPR RNA的成熟

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摘要

Prokaryotic immunity against foreign nucleic acids mediated by clustered, regularly interspaced, short palindromic repeats (CRISPR) depends on the expression of the CRISPR-associated (Cas) proteins and the formation of small CRISPR RNAs (crRNAs). The crRNA-loaded Cas ribonucleoprotein complexes convey the specific recognition and inactivation of target nucleic acids. In E. coli K12, the maturation of crRNAs and the interference with target DNA is performed by the Cascade complex. The transcription of the Cascade operon is tightly repressed through H-NS-dependent inhibition of the Pcas promoter. Elevated levels of the LysR-type regulator LeuO induce the Pcas promoter and concomitantly activate the CRISPR-mediated immunity against phages. Here, we show that the Pcas promoter can also be induced by constitutive expression of the regulator BglJ. This activation is LeuO-dependent as heterodimers of BglJ and RcsB activate leuO transcription. Each transcription factor, LeuO or BglJ, induced the transcription of the Cascade genes to comparable amounts. However, the maturation of the crRNAs was activated in LeuO but not in BglJ-expressing cells. Studies on CRISPR promoter activities, transcript stabilities, crRNA processing and Cascade protein levels were performed to answer the question why crRNA maturation is defective in BglJ-expressing cells. Our results demonstrate that the activation of Cascade gene transcription is necessary but not sufficient to turn on the CRISPR-mediated immunity and suggest a more complex regulation of the type I-E CRISPR-Cas system in E. coli.
机译:由簇状,规则间隔的短回文重复序列(CRISPR)介导的针对外来核酸的原核免疫取决于CRISPR相关(Cas)蛋白的表达和小的CRISPR RNA(crRNA)的形成。加载crRNA的Cas核糖核蛋白复合物可传达对靶核酸的特异性识别和灭活作用。在大肠杆菌K12中,crRNA的成熟和对靶DNA的干扰是由Cascade复合物完成的。通过H-NS依赖的Pcas启动子抑制,紧密抑制Cascade操纵子的转录。 LysR型调节剂LeuO的水平升高会诱导Pcas启动子,并同时激活CRISPR介导的针对噬菌体的免疫力。在这里,我们表明Pcas启动子也可以通过调节剂BglJ的组成型表达来诱导。这种激活是LeuO依赖性的,因为BglJ和RcsB的异二聚体激活leuO转录。每个转录因子LeuO或BglJ诱导Cascade基因的转录达到可比的水平。但是,crRNA的成熟在LeuO中被激活,而在BglJ表达细胞中未被激活。进行了CRISPR启动子活性,转录稳定性,crRNA加工和Cascade蛋白水平的研究,以回答为什么crRNA成熟在表达BglJ的细胞中有缺陷的问题。我们的结果表明,级联基因转录的激活是必需的,但不足以开启CRISPR介导的免疫,并提示对大肠杆菌中I-E CRISPR-Cas系统的调控更为复杂。

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