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超越即插即用:人工新霉素核糖开关的上下文敏感性与设计。

Beyond Plug and Pray: Context Sensitivity and Design of Artificial Neomycin Riboswitches.

机构信息

Institute for Biochemistry, Leipzig University, Brüderstraße 34, D-04103 Leipzig, Germany.

Bioinformatics Group, Institute of Computer Science, and Interdisciplinary Center for Bioinformatics, Leipzig University, Härtelstraße 16-18, D-04107 Leipzig, Germany.

出版信息

RNA Biol. 2021 Apr;18(4):457-467. doi: 10.1080/15476286.2020.1816336. Epub 2020 Oct 25.

Abstract

Gene regulation in prokaryotes often depends on RNA elements such as riboswitches or RNA thermometers located in the 5' untranslated region of mRNA. Rearrangements of the RNA structure in response, e.g., to the binding of small molecules or ions control translational initiation or premature termination of transcription and thus mRNA expression. Such structural responses are amenable to computational modelling, making it possible to rationally design synthetic riboswitches for a given aptamer. Starting from an artificial aptamer, we construct the first synthetic transcriptional riboswitches that respond to the antibiotic neomycin. We show that the switching behaviour critically depends not only on the sequence of the riboswitch itself, but also on its sequence context. We therefore developed methods to predict the impact of the context, making it possible to adapt the design and to rescue non-functional riboswitches. We furthermore analyse the influence of 5' hairpins with varying stability on neomycin riboswitch activity. Our data highlight the limitations of a simple plug-and-play approach in the design of complex genetic circuits and demonstrate that detailed computational models significantly simplify, improve, and automate the design of transcriptional circuits. Our design software is available under a free licence on GitHub (https://github.com/xileF1337/riboswitch_design).

摘要

原核生物中的基因调控通常依赖于 RNA 元件,例如位于 mRNA 5' 非翻译区的核糖开关或 RNA 温度计。RNA 结构的重排会响应小分子或离子的结合,从而控制翻译起始或转录的过早终止,从而控制 mRNA 的表达。这种结构响应适用于计算建模,从而可以为给定的适体合理设计合成核糖开关。我们从人工适体出发,构建了第一个对抗生素新霉素有反应的合成转录核糖开关。我们表明,开关行为不仅取决于核糖开关本身的序列,还取决于其序列环境。因此,我们开发了预测上下文影响的方法,使设计能够适应并拯救非功能的核糖开关。我们还分析了具有不同稳定性的 5' 发夹对新霉素核糖开关活性的影响。我们的数据强调了在设计复杂遗传电路时简单的即插即用方法的局限性,并证明了详细的计算模型可以大大简化、改进和自动化转录电路的设计。我们的设计软件可在 GitHub 上免费获得(https://github.com/xileF1337/riboswitch_design)。

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Microbiol Spectr. 2018 May;6(3). doi: 10.1128/microbiolspec.RWR-0007-2017.
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Synthetic Riboswitches: From Plug and Pray toward Plug and Play.合成核糖开关:从“插电祈祷”到“即插即用”
Biochemistry. 2017 Mar 7;56(9):1181-1198. doi: 10.1021/acs.biochem.6b01218. Epub 2017 Feb 24.
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