Engineered circular guide RNAs enhance miniature CRISPR/Cas12f-based gene activation and adenine base editing

CRISPR system has been widely used due to its precision and versatility in gene editing. Un1Cas12f1 from uncultured archaeon (hereafter referred to as Cas12f), known for its compact size (529 aa), exhibits obvious delivery advantage for gene editing in vitro and in vivo. However, its activity remains suboptimal. In this study, we engineer circular guide RNA (cgRNA) for Cas12f and significantly improve the efficiency of gene activation about 1.9-19.2-fold. When combined with a phase separation system, the activation efficiency is further increased about 2.3-3.9-fold. In addition, cgRNA enhances the editing efficiency and narrows the editing window of adenine base editing about 1.2-2.5-fold. Importantly, this optimization strategy also boosts the Cas12f-induced gene activation efficiency in mouse liver. Therefore, we demonstrate that cgRNA is able to enhance Cas12f-based gene activation and adenine base editing, which holds great potential for gene therapy.

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Publication Details

Journal
Nature Communications
Published
2025-03-28
DOI
https://doi.org/10.1038/s41467-025-58367-4
Citations
16
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
12.90
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article

Engineered circular guide RNAs enhance miniature CRISPR/Cas12f-based gene activation and adenine base editing

Ying Lin, Hongxin Huang, Kechen Chen, Mengrao Li et al.
16 citations
Nature Communications
CRISPR and Genetic Engineering
12.90
article

Engineered circular guide RNAs enhance miniature CRISPR/Cas12f-based gene activation and adenine base editing

Ying Lin, Hongxin Huang, Kechen Chen, Mengrao Li, Shufeng Ma, Kaitong Liao, Yanqun Zhang, Zhili Rong, Jiawei Liu, Xin Zhang, Yu‐Chen Liu, Mei Wang, Jiayi Zhou, Jiahong Wang, Tao Huang
article en
16 citations

Abstract

CRISPR system has been widely used due to its precision and versatility in gene editing. Un1Cas12f1 from uncultured archaeon (hereafter referred to as Cas12f), known for its compact size (529 aa), exhibits obvious delivery advantage for gene editing in vitro and in vivo. However, its activity remains suboptimal. In this study, we engineer circular guide RNA (cgRNA) for Cas12f and significantly improve the efficiency of gene activation about 1.9-19.2-fold. When combined with a phase separation system, the activation efficiency is further increased about 2.3-3.9-fold. In addition, cgRNA enhances the editing efficiency and narrows the editing window of adenine base editing about 1.2-2.5-fold. Importantly, this optimization strategy also boosts the Cas12f-induced gene activation efficiency in mouse liver. Therefore, we demonstrate that cgRNA is able to enhance Cas12f-based gene activation and adenine base editing, which holds great potential for gene therapy.

Nature CommunicationsVol. 16(1)
First Affiliated Hospital of Guangzhou Medical University (CN), State Key Laboratory of Respiratory Disease (CN), Southern Medical University (CN), Guangzhou Medical University (CN)
Zero hunger
Openalex Percentile: Top 1%
CRISPR and Genetic Engineering
12.90
DOIOpen Access PDFOpenAlex
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