| Literature DB >> 32882151 |
Christian Günzel1, Felix Kühnl2, Katharina Arnold1, Sven Findeiß2, Christina E Weinberg1, Peter F Stadler2,3,4,5,6, Mario Mörl1.
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 in vivo critically depends not only on the sequence of the riboswitch itself, but also on its sequence context. We therefore developed in silico 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).Entities:
Keywords: N1 aptamer; Riboswitch design; context optimization; decoupling leader; leader hairpin; neomycin aptamer; regulatory RNA; synthetic riboswitch; transcription regulation
Year: 2020 PMID: 32882151 PMCID: PMC7971258 DOI: 10.1080/15476286.2020.1816336
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652