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Predictable control of RNA lifetime using engineered degradation-tuning RNAs

The ability to tune RNA and gene expression dynamics is greatly needed for biotechnological applications. Native RNA stabilizers or engineered 5’ stability hairpins have been utilized to regulate transcript half-life to control recombinant protein expression. However, these methods have been mostly...

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Detalles Bibliográficos
Autores principales: Zhang, Qi, Ma, Duo, Wu, Fuqing, Standage-Beier, Kylie, Chen, Xingwen, Wu, Kaiyue, Green, Alexander A., Wang, Xiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238901/
https://www.ncbi.nlm.nih.gov/pubmed/34155402
http://dx.doi.org/10.1038/s41589-021-00816-4
Descripción
Sumario:The ability to tune RNA and gene expression dynamics is greatly needed for biotechnological applications. Native RNA stabilizers or engineered 5’ stability hairpins have been utilized to regulate transcript half-life to control recombinant protein expression. However, these methods have been mostly ad-hoc and hence lack predictability and modularity. Here, we report a library of RNA modules called degradation-tuning RNAs (dtRNAs) that can increase or decrease transcript stability in vivo and in vitro. dtRNAs enable modulation of transcript stability over a 40-fold dynamic range in Escherichia coli with minimal influence on translation initiation. We harness dtRNAs in mRNAs and noncoding RNAs to tune gene circuit dynamics and enhance CRISPR interference in vivo. Use of stabilizing dtRNAs in cell-free transcription-translation reactions also tunes gene and RNA aptamer production. Finally, we combine dtRNAs with toehold switch sensors to enhance the performance of paper-based norovirus diagnostics, illustrating the potential of dtRNAs for biotechnological applications.