» Articles » PMID: 34833155

Detection of Island MRNAs Using Toehold Sensors in

Overview
Journal Life (Basel)
Specialty Biology
Date 2021 Nov 27
PMID 34833155
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Synthetic biologists have applied biomolecular engineering approaches toward the goal of novel biological devices and have shown progress in diverse areas of medicine and biotechnology. Especially promising is the application of synthetic biological devices towards a novel class of molecular diagnostics. As an example, a de-novo-designed riboregulator called toehold switch, with its programmability and compatibility with field-deployable devices showed promising in vitro applications for viral RNA detection such as Zika and Corona viruses. However, the in vivo application of high-performance RNA sensors remains challenging due to the secondary structure of long mRNA species. Here, we introduced 'Helper RNAs' that can enhance the functionality of toehold switch sensors by mitigating the effect of secondary structures around a target site. By employing the helper RNAs, previously reported mRNA sensor showed improved fold-changes in vivo. To further generalize the Helper RNA approaches, we employed automatic design pipeline for toehold sensors that target the essential genes within the island, an important target of biomedical research in connection with colorectal cancer. The toehold switch sensors showed fold-changes upon the expression of full-length mRNAs that apparently depended sensitively on the identity of the gene as well as the predicted local structure within the target region of the mRNA. Still, the helper RNAs could improve the performance of toehold switch sensors in many instances, with up to 10-fold improvement over no helper cases. These results suggest that the helper RNA approaches can further assist the design of functional RNA devices in vivo with the aid of the streamlined automatic design software developed here. Further, our solutions for screening and stabilizing single-stranded region of mRNA may find use in other in vivo mRNA-sensing applications such as cas13 crRNA design, transcriptome engineering, and trans-cleaving ribozymes.

Citing Articles

Making target sites in large structured RNAs accessible to RNA-cleaving DNAzymes through hybridization with synthetic DNA oligonucleotides.

Nurmi C, Gu J, Mathai A, Brennan J, Li Y Nucleic Acids Res. 2024; 52(18):11177-11187.

PMID: 39248110 PMC: 11472044. DOI: 10.1093/nar/gkae778.


RNA-Based Sensor Systems for Affordable Diagnostics in the Age of Pandemics.

Koksaldi I, Park D, Atilla A, Kang H, Kim J, Safak Seker U ACS Synth Biol. 2024; 13(4):1026-1037.

PMID: 38588603 PMC: 11036506. DOI: 10.1021/acssynbio.3c00698.


Regulatory RNAs in A review on regulatory mechanism and applications in synthetic biology.

Peng A, Yin G, Zuo W, Zhang L, Du G, Chen J Synth Syst Biotechnol. 2024; 9(2):223-233.

PMID: 38385150 PMC: 10877136. DOI: 10.1016/j.synbio.2024.01.013.


Synthetic Genetic Elements, Devices, and Systems.

Kato Y, Lou C Life (Basel). 2022; 12(7).

PMID: 35888035 PMC: 9320439. DOI: 10.3390/life12070945.

References
1.
Ran F, Cong L, Yan W, Scott D, Gootenberg J, Kriz A . In vivo genome editing using Staphylococcus aureus Cas9. Nature. 2015; 520(7546):186-91. PMC: 4393360. DOI: 10.1038/nature14299. View

2.
Hsu B, Plant I, Lyon L, Anastassacos F, Way J, Silver P . In situ reprogramming of gut bacteria by oral delivery. Nat Commun. 2020; 11(1):5030. PMC: 7538559. DOI: 10.1038/s41467-020-18614-2. View

3.
Fornace M, Porubsky N, Pierce N . A Unified Dynamic Programming Framework for the Analysis of Interacting Nucleic Acid Strands: Enhanced Models, Scalability, and Speed. ACS Synth Biol. 2020; 9(10):2665-2678. DOI: 10.1021/acssynbio.9b00523. View

4.
Chang W, Liu W, Shen H, Chen S, Liao P, Liu Y . Molecular AND logic gate for multiple single-nucleotide mutations detection based on CRISPR/Cas9n system-trigged signal amplification. Anal Chim Acta. 2020; 1112:46-53. DOI: 10.1016/j.aca.2020.03.058. View

5.
Romano J, WILLIAMS K, Shurtliff R, Ginocchio C, Kaplan M . NASBA technology: isothermal RNA amplification in qualitative and quantitative diagnostics. Immunol Invest. 1997; 26(1-2):15-28. DOI: 10.3109/08820139709048912. View