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加工过程产生 RNA 3' 端,从而掩盖原核生物中转录终止事件。

Processing generates 3' ends of RNA masking transcription termination events in prokaryotes.

机构信息

State Key Laboratory of Agricultural Microbiology, College of Life Science and Technology, Huazhong Agricultural University, Wuhan, Hubei 430070, People's Republic of China.

Department of Biological Sciences, College of Biological Sciences and Biotechnology, Chungnam National University, 305-764 Daejeon, Republic of Korea.

出版信息

Proc Natl Acad Sci U S A. 2019 Mar 5;116(10):4440-4445. doi: 10.1073/pnas.1813181116. Epub 2019 Feb 19.

Abstract

Two kinds of signal-dependent transcription termination and RNA release mechanisms have been established in prokaryotes in vitro by: () binding of Rho to cytidine-rich nascent RNA [Rho-dependent termination (RDT)], and () the formation of a hairpin structure in the nascent RNA, ending predominantly with uridine residues [Rho-independent termination (RIT)]. As shown here, the two signals act independently of each other and can be regulated (suppressed) by translation-transcription coupling in vivo. When not suppressed, both RIT- and RDT-mediated transcription termination do occur, but ribonucleolytic processing generates defined new 3' ends in the terminated RNA molecules. The actual termination events at the end of transcription units are masked by generation of new processed 3' RNA ends; thus the in vivo 3' ends do not define termination sites. We predict generation of 3' ends of mRNA by processing is a common phenomenon in prokaryotes as is the case in eukaryotes.

摘要

两种信号依赖的转录终止和 RNA 释放机制已经在体外的原核生物中得到证实:()Rho 与富含胞嘧啶的新生 RNA 结合 [Rho 依赖性终止(RDT)],以及()新生 RNA 中发夹结构的形成,主要以尿嘧啶残基结尾 [Rho 非依赖性终止(RIT)]。如本文所示,这两个信号相互独立,可以在体内通过翻译转录偶联进行调节(抑制)。当不受抑制时,RIT 和 RDT 介导的转录终止都会发生,但核糖核酸酶处理会在终止的 RNA 分子中生成定义明确的新 3' 末端。转录单元末端的实际终止事件被生成新的加工 3' RNA 末端所掩盖;因此,体内的 3' 末端不能定义终止位点。我们预测,通过加工生成 mRNA 的 3' 末端是原核生物中的一种常见现象,就像真核生物一样。

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