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内在和 Rho 依赖性终止协同作用,以在 3'非翻译区实现高效转录终止。

Intrinsic and Rho-dependent termination cooperate for efficient transcription termination at 3' untranslated regions.

机构信息

Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, 560012, India.

Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, 560012, India; Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, 560012, India.

出版信息

Biochem Biophys Res Commun. 2022 Nov 5;628:123-132. doi: 10.1016/j.bbrc.2022.08.063. Epub 2022 Sep 1.

Abstract

The intrinsic, and the Rho-dependent mechanisms of transcription termination are conserved in bacteria. Generally, the two mechanisms have been illustrated as two independent pathways occurring in the 3' ends of different genes with contrasting requirements to halt RNA synthesis. However, a majority of intrinsic terminators terminate transcription inefficiently leading to transcriptional read-through. The unwanted transcription in the downstream region beyond the terminator would have undesired consequences. To prevent such transcriptional read-through, bacteria must have evolved ways to terminate transcription more efficiently at or near the termination sites. We describe the participation of both the mechanisms, where intrinsic terminator and Rho factor contribute to prevent transcriptional read-through. Contribution from both the termination processes is demonstrated at the downstream regions of the genes both in vitro and in vivo in mycobacteria. Distinct patterns of cooperation between the two modes of termination were observed at the 3' untranslated regions of the genes to ensure efficient termination. We demonstrate similar mode of operation between the two termination processes in Escherichia coli suggesting a likely prevalence of this cooperation across bacteria. The reporter system developed to assess the Rho - intrinsic termination collaboration in vivo for mycobacteria and E. coli can readily be applied to other bacteria.

摘要

在细菌中,转录终止的内在和 Rho 依赖性机制是保守的。一般来说,这两种机制被描述为两种独立的途径,发生在不同基因的 3' 末端,具有相反的停止 RNA 合成的要求。然而,大多数内在终止子在终止子之后的下游区域终止转录效率低下,导致转录通读。终止子下游区域的不想要的转录会产生不良后果。为了防止这种转录通读,细菌必须进化出更有效地在终止位点或附近终止转录的方法。我们描述了这两种机制的参与,其中内在终止子和 Rho 因子有助于防止转录通读。在体外和体内分枝杆菌的基因下游区域都证明了两种终止过程的贡献。在基因的 3' 非翻译区观察到两种终止模式之间的合作模式,以确保有效的终止。我们在大肠杆菌中观察到两种终止过程之间类似的操作模式,这表明这种合作在细菌中可能很普遍。为分枝杆菌和大肠杆菌开发的评估体内 Rho-内在终止协作的报告系统可以很容易地应用于其他细菌。

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