Template nicking suppresses promoter-independent antisense transcription in IVT via R-loop-mediated strand displacement

In vitro transcription (IVT) using T7 RNA polymerase is a cornerstone technology for synthetic messenger RNA (mRNA) production. However, a persistent challenge is the formation of immunogenic double-stranded RNA (dsRNA) byproducts, primarily arising from promoter-independent antisense transcription at free DNA ends. Here, we introduce the nicked low dsRNA template (NiLoT) strategy, a template engineering approach in which a single-strand nick is placed in the non-template DNA strand to promote R-loop formation and suppress antisense RNA synthesis. NiLoT significantly reduces dsRNA contamination without compromising RNA yield and enhances translational output while minimizing innate immune activation in human cells. This broadly applicable method improves IVT mRNA quality and supports more efficient and scalable RNA production.

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Publication Details

Journal
Nucleic Acids Research
Published
2026-01-07
DOI
https://doi.org/10.1093/nar/gkaf1536
Primary Topic
RNA regulation and disease
Type
article
Field-Weighted Citation Impact
0.00

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article

Template nicking suppresses promoter-independent antisense transcription in IVT via R-loop-mediated strand displacement

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Nucleic Acids Research
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article

Template nicking suppresses promoter-independent antisense transcription in IVT via R-loop-mediated strand displacement

Woo-Chul Noh, Goeun Lee, Junhyung Ryu, Jinmin Jang, Dong-Eun Kim
article en

Abstract

In vitro transcription (IVT) using T7 RNA polymerase is a cornerstone technology for synthetic messenger RNA (mRNA) production. However, a persistent challenge is the formation of immunogenic double-stranded RNA (dsRNA) byproducts, primarily arising from promoter-independent antisense transcription at free DNA ends. Here, we introduce the nicked low dsRNA template (NiLoT) strategy, a template engineering approach in which a single-strand nick is placed in the non-template DNA strand to promote R-loop formation and suppress antisense RNA synthesis. NiLoT significantly reduces dsRNA contamination without compromising RNA yield and enhances translational output while minimizing innate immune activation in human cells. This broadly applicable method improves IVT mRNA quality and supports more efficient and scalable RNA production.

Nucleic Acids ResearchVol. 54(2)
Konkuk University (KR), Daewon Pharm (South Korea) (KR)
National Research Foundation, Konkuk University, National Research Foundation of Korea, Ministry of Science and ICT, South Korea
Openalex Percentile: Top 87%
RNA regulation and disease
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