Programmable in vivo mRNA circularization for enhanced gene expression in bacteria
2026 · Nucleic Acids Research
저자
Seongjun Park, Giho Kim, Min Ha Kim, Yong Hee Han, Geunyung Park, Gibyuck Byun, Hyeonwoo Mun, Ho Joon Kim, 서상우 (Sang Woo Seo)
연구주제
RNA and protein synthesis mechanisms · Microbial Metabolic Engineering and Bioproduction · Bacterial Genetics and Biotechnology
NTIS 과학기술표준분류
가장 가까운 분류(생명과학 > 생물공학)가 화학·화공 범위 밖이다. 배정 근거: 지원 과제·키워드 근거가 없어 AI가 논문 제목·초록을 읽고 고른 분류.
AI 연구 키워드·방법
bacterial gene expression mrna circularization mrna stability protein expression enhancement
키워드 (OpenAlex)
mRNA circularization bacterial gene expression mRNA stability protein expression microbial cell factories
초록
The minute-scale lifetime of mRNA strongly influences bacterial gene expression, whereas a robust and programmable approach to directly control the mRNA stability and topology remains elusive. Here, we develop CRESEnT (Circular RNA Expression for Stable and Enhanced Translation), a programmable in vivo mRNA circularization system based on a permuted intron-exon architecture to engineer mRNA topology. CRESEnT enables facile circularization of mRNA, which led to a substantial increase in protein expression across diverse promoters, RBS variants, genetic cargos, and bacterial hosts. Furthermore, application of CRESEnT to biosynthetic pathways increased the production of several value-added metabolites, demonstrating that mRNA circularization can be harnessed to improve the metabolic performance of microbial cell factories. Together, these results establish RNA topology engineering via circu…
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