| Literature DB >> 27840078 |
Yen-Hsiang Wang1, Maureen McKeague1, Tammy M Hsu1, Christina D Smolke2.
Abstract
For synthetic biology applications, protein-based transcriptional genetic controllers are limited in terms of orthogonality, modularity, and portability. Although ribozyme-based switches can address these issues, their current two-stage architectures and limited dynamic range hinder their broader incorporation into systems-level genetic controllers. Here, we address these challenges by implementing an RNA-protein hybrid controller with a three-stage architecture that introduces a transcription-based amplifier between an RNA sensor and a protein actuator. To facilitate the construction of these more complex circuits, we use a model-guided strategy to efficiently match the activities of stages. The presence of the amplifier enabled the three-stage controller to have up to 200-fold higher gene expression than its two-stage counterpart and made it possible to implement higher-order controllers, such as multilayer Boolean logic and feedback systems. The modularity inherent in the three-stage architecture along with the sensing flexibility of RNA devices presents a generalizable framework for designing and building sophisticated genetic control systems.Entities:
Keywords: RNA controllers; closed-loop feedback; genetic amplifiers; model-guided design; synthetic biology
Year: 2016 PMID: 27840078 PMCID: PMC5182110 DOI: 10.1016/j.cels.2016.10.008
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304