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Rho and NusG suppress pervasive antisense transcription in Escherichia coli

机译:Rho和NusG抑制大肠杆菌中普遍存在的反义转录

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摘要

Despite the prevalence of antisense transcripts in bacterial transcriptomes, little is known about how their synthesis is controlled. We report that a major function of the Escherichia coli termination factor Rho and its cofactor, NusG, is suppression of ubiquitous antisense transcription genome-wide. Rho binds C-rich unstructured nascent RNA (high C/G ratio) prior to its ATP-dependent dissociation of transcription complexes. NusG is required for efficient termination at minority subsets (~20%) of both antisense and sense Rho-dependent terminators with lower C/G ratio sequences. In contrast, a widely studied nusA deletion proposed to compromise Rho-dependent termination had no effect on antisense or sense Rho-dependent terminators in vivo. Global colocalization of the histone-like nucleoid-structuring protein (H-NS) with Rho-dependent terminators and genetic interactions between hns and rho suggest that H-NS aids Rho in suppression of antisense transcription. The combined actions of Rho, NusG, and H-NS appear to be analogous to the Sen1-Nrd1-Nab3 and nucleosome systems that suppress antisense transcription in eukaryotes.
机译:尽管反义转录物在细菌转录组中普遍存在,但对其合成的控制方式知之甚少。我们报告说,大肠杆菌终止因子Rho及其辅因子NusG的主要功能是抑制遍在全基因组的反义转录。 Rho在其ATP依赖的转录复合体解离之前,先结合富含C的非结构化新生RNA(高C / G比)。 NusG是在具有较低C / G比序列的反义和有义Rho依赖终止子的少数子集(约20%)处有效终止所必需的。相比之下,广泛研究的提议破坏Nho依赖性终止的nusA缺失对体内反义或有义Rho依赖性终止子没有影响。组蛋白样核糖结构蛋白(H-NS)与Rho依赖性终止子的全球共定位以及hns和rho之间的遗传相互作用表明H-NS有助于Rho抑制反义转录。 Rho,NusG和H-NS的联合作用似乎类似于抑制真核生物中反义转录的Sen1-Nrd1-Nab3和核小体系统。

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