Literature DB >> 25826571

Design criteria for synthetic riboswitches acting on transcription.

Manja Wachsmuth1, Gesine Domin, Ronny Lorenz, Robert Serfling, Sven Findeiß, Peter F Stadler, Mario Mörl.   

Abstract

Riboswitches are RNA-based regulators of gene expression composed of a ligand-sensing aptamer domain followed by an overlapping expression platform. The regulation occurs at either the level of transcription (by formation of terminator or antiterminator structures) or translation (by presentation or sequestering of the ribosomal binding site). Due to a modular composition, these elements can be manipulated by combining different aptamers and expression platforms and therefore represent useful tools to regulate gene expression in synthetic biology. Using computationally designed theophylline-dependent riboswitches we show that 2 parameters, terminator hairpin stability and folding traps, have a major impact on the functionality of the designed constructs. These have to be considered very carefully during design phase. Furthermore, a combination of several copies of individual riboswitches leads to a much improved activation ratio between induced and uninduced gene activity and to a linear dose-dependent increase in reporter gene expression. Such serial arrangements of synthetic riboswitches closely resemble their natural counterparts and may form the basis for simple quantitative read out systems for the detection of specific target molecules in the cell.

Entities:  

Keywords:  GFP, green fluorescent protein; MU, Miller units; PCR, polymerase chain reaction; RS, riboswitch; bgaB, B. stearothermophilus-derived beta-galactosidase; riboswitch design; synthetic biology; synthetic riboswitch; tandem riboswitch; theophylline aptamer; transcription regulation

Mesh:

Substances:

Year:  2015        PMID: 25826571      PMCID: PMC4615730          DOI: 10.1080/15476286.2015.1017235

Source DB:  PubMed          Journal:  RNA Biol        ISSN: 1547-6286            Impact factor:   4.652


  41 in total

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2.  Exploring the complex folding kinetics of RNA hairpins: II. Effect of sequence, length, and misfolded states.

Authors:  Wenbing Zhang; Shi-Jie Chen
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3.  Tandem riboswitch architectures exhibit complex gene control functions.

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4.  Folding kinetics of large RNAs.

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5.  Genetic control of mammalian T-cell proliferation with synthetic RNA regulatory systems.

Authors:  Yvonne Y Chen; Michael C Jensen; Christina D Smolke
Journal:  Proc Natl Acad Sci U S A       Date:  2010-04-26       Impact factor: 11.205

6.  Ligand binding and gene control characteristics of tandem riboswitches in Bacillus anthracis.

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Journal:  RNA       Date:  2007-02-16       Impact factor: 4.942

7.  ViennaRNA Package 2.0.

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8.  Prediction of transcriptional terminators in Bacillus subtilis and related species.

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9.  Measurement and modeling of intrinsic transcription terminators.

Authors:  Guillaume Cambray; Joao C Guimaraes; Vivek K Mutalik; Colin Lam; Quynh-Anh Mai; Tim Thimmaiah; James M Carothers; Adam P Arkin; Drew Endy
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10.  Translation rate is controlled by coupled trade-offs between site accessibility, selective RNA unfolding and sliding at upstream standby sites.

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  16 in total

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

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Journal:  RNA Biol       Date:  2020-10-25       Impact factor: 4.652

2.  Automated physics-based design of synthetic riboswitches from diverse RNA aptamers.

Authors:  Amin Espah Borujeni; Dennis M Mishler; Jingzhi Wang; Walker Huso; Howard M Salis
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4.  Synthetic riboswitches for the analysis of tRNA processing by eukaryotic RNase P enzymes.

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Review 6.  Synthetic Biology of Small RNAs and Riboswitches.

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Journal:  Sci Rep       Date:  2016-02-19       Impact factor: 4.379

8.  Using sliding mode observers to estimate BtuB concentration from measured vitamin B12 concentration.

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9.  RNA folding with hard and soft constraints.

Authors:  Ronny Lorenz; Ivo L Hofacker; Peter F Stadler
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10.  Computational design of small transcription activating RNAs for versatile and dynamic gene regulation.

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