Key result
Artificial eukaryotic OFF-riboswitches ligand-dose-dependently downregulated IRES-mediated translation without hybridization switches, resulting in higher switching efficiency.
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Novel hybridization-switch-free OFF-riboswitches provide efficient, ligand-dose-dependent downregulation of translation in eukaryotic cell-free systems, offering a versatile tool for synthetic biology.
We constructed novel artificial riboswitches that function in a eukaryotic translation system (wheat germ extract), by rationally implanting an in vitro-selected aptamer into the intergenic internal ribosome entry site (IRES) of Plautia stali intestine virus. These eukaryotic OFF-riboswitches (OFF-eRSs) ligand-dose-dependently downregulate IRES-mediated translation without hybridization switches, which typical riboswitches utilize for gene regulation. The hybridization-switch-free mechanism not only allows for easy design but also requires less energy for regulation, resulting in a higher switching efficiency than hybridization-switch-based OFF-eRSs provide. In addition, even a small ligand such as theophylline can induce satisfactory repression, in contrast to other types of OFF-eRSs that modulate the 5' cap-dependent canonical translation. Because our proposed hybridization-switch-free OFF-eRSs are based on a versatile IRES that functions well in many types of eukaryotic translation systems, they would be widely usable elements for synthetic gene circuits in both cell-free and cell-based synthetic biology.
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Ogawa et al. (2017) studied this question. Artificial OFF-Riboswitches (OFF-eRSs) vs. Hybridization-switch-based OFF-eRSs was evaluated on IRES-mediated translation downregulation. Artificial eukaryotic OFF-riboswitches ligand-dose-dependently downregulated IRES-mediated translation without hybridization switches, resulting in higher switching efficiency.
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