Engineering modular 'ON' RNA switches using biological components

被引:69
作者
Ceres, Pablo [1 ]
Trausch, Jeremiah J. [1 ]
Batey, Robert T. [1 ]
机构
[1] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
GENE-EXPRESSION; S-ADENOSYLMETHIONINE; SYNTHETIC BIOLOGY; TRANSCRIPTION TERMINATION; RIBOSWITCHES; MECHANISM; BINDING; EVOLUTION; ADENOSYLHOMOCYSTEINE; RECOGNITION;
D O I
10.1093/nar/gkt787
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Riboswitches are cis-acting regulatory elements broadly distributed in bacterial mRNAs that control a wide range of critical metabolic activities. Expression is governed by two distinct domains within the mRNA leader: a sensory 'aptamer domain' and a regulatory 'expression platform'. Riboswitches have also received considerable attention as important tools in synthetic biology because of their conceptually simple structure and the ability to obtain aptamers that bind almost any conceivable small molecule using in vitro selection (referred to as SELEX). In the design of artificial riboswitches, a significant hurdle has been to couple the two domains enabling their efficient communication. We previously demonstrated that biological transcriptional 'OFF' expression platforms are easily coupled to diverse aptamers, both biological and SELEX-derived, using simple design rules. Here, we present two modular transcriptional 'ON' riboswitch expression platforms that are also capable of hosting foreign aptamers. We demonstrate that these biological parts can be used to facilely generate artificial chimeric riboswitches capable of robustly regulating transcription both in vitro and in vivo. We expect that these modular expression platforms will be of great utility for various synthetic biological applications that use RNA-based biosensors.
引用
收藏
页码:10449 / 10461
页数:13
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