新型コロナウイルスの翻訳阻害に耐性をもつ修飾mRNAの合成と排他的セレクタ遺伝子回路の構築

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2025-06-19 京都大学iPS細胞研究所

新型コロナウイルスの翻訳阻害に耐性をもつ修飾mRNAの合成と排他的セレクタ遺伝子回路の構築

新型コロナウイルス(SARS-CoV-2)が翻訳阻害に用いるNsp1タンパク質に耐性をもつ修飾mRNAの合成に成功し、この耐性を応用した「排他的セレクタ遺伝子回路」が初めて構築された。研究では、ウイルス由来の5’UTR配列とヌクレオシド修飾(m1Ψ+m5C)を組み合わせ、Nsp1の抑制を回避。毒性タンパク質Barnaseとその抑制因子Barstarを使い、Nsp1存在下でのみ毒性を発揮するシステムも開発された。mRNA医療や感染症制御への応用が期待される。

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SARS-CoV-2のNsp1耐性修飾RNAによるNsp1応答性システムの創製 SARS-CoV-2 Nsp1-Resistant Modified RNA for the Creation of Nsp1-Responsive Systems

Malvin Leonardo Pardi,Kazuo Takayama,Hirohide Saito
ACS Synthetic Biology  Published: June 5, 2025
DOI:https://doi.org/10.1021/acssynbio.5c00075

Abstract

Modified RNA (modRNA) facilitates the introduction of complex synthetic genetic circuits into cells without the risk of genomic integration, opening up the implementation of synthetic circuits as therapeutics. However, the number of protein-RNA interfaces that are suitable for the construction of protein-responsive modRNA switches as well as the lack of protein-responsive exclusive selector systems stifles the development of RNA-based synthetic circuits. Here, we present the creation of a modRNA capable of resisting the effects of Nsp1 for the reliable expression of its coding sequence. Using both the subgenomic viral RNA 5′UTR and two modified nucleosides, we observed efficient exogenous protein expression even in Nsp1-transfected cells. To demonstrate its utility, we developed a barnase-barstar system capable of conditional transcript suppression in the presence of Nsp1. Altogether, the resistance to Nsp1-mediated translational suppression and the resulting Nsp1-sensing system we present in this study provide an invaluable opportunity to develop a new class of protein-sensing systems for the construction of more complex RNA-based genetic circuits.

生物工学一般
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