Tailoring Cas12a functionality with a user-friendly and versatile crRNA variant toolbox

Cas12a, with its unique targeting and cleavage activity towards DNA, has been widely applied in gene editing and molecular diagnostics. However, there currently lacks an activity regulation strategy that combines flexibility and simplicity to adapt Cas12a to different demands across various application scenarios. In this study, we present a simple yet effective strategy, wherein we systematically mutate the crRNA direct repeat (DR) sequence to uncover a range of distinct crRNA mutants, which are then compiled into a crRNA toolbox to enable flexible regulation of Cas12a activity. By harnessing the complementarity and synergy between these mutants, we successfully enhance Cas12a performance across various application scenarios. Our crRNA toolbox enables fine-tuned control over expression levels, improves base editing accuracy, enhances transformation and editing efficiency in prokaryote homologous recombination-mediated gene editing, and facilitates rapid, accurate, one-pot, semi-quantitative nucleic acid diagnostics. In summary, the DR sequence mutation strategy provides simple, flexible, and diverse options for Cas12a activity regulation and functional optimization.

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Publication Details

Journal
Nature Communications
Published
2025-10-08
DOI
https://doi.org/10.1038/s41467-025-64010-z
Citations
8
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
6.45

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article

Tailoring Cas12a functionality with a user-friendly and versatile crRNA variant toolbox

Jie‐Jie Chen, Jing Han, Zhou‐Hua Cheng, Dong‐Feng Liu et al.
8 citations
Nature Communications
CRISPR and Genetic Engineering
6.45
article

Tailoring Cas12a functionality with a user-friendly and versatile crRNA variant toolbox

Jie‐Jie Chen, Jing Han, Zhou‐Hua Cheng, Dong‐Feng Liu, Lan Hu, Han‐Qing Yu, Xiaofan Li, Shuxia Zhang, Min Yuan
article en
8 citations

Abstract

Cas12a, with its unique targeting and cleavage activity towards DNA, has been widely applied in gene editing and molecular diagnostics. However, there currently lacks an activity regulation strategy that combines flexibility and simplicity to adapt Cas12a to different demands across various application scenarios. In this study, we present a simple yet effective strategy, wherein we systematically mutate the crRNA direct repeat (DR) sequence to uncover a range of distinct crRNA mutants, which are then compiled into a crRNA toolbox to enable flexible regulation of Cas12a activity. By harnessing the complementarity and synergy between these mutants, we successfully enhance Cas12a performance across various application scenarios. Our crRNA toolbox enables fine-tuned control over expression levels, improves base editing accuracy, enhances transformation and editing efficiency in prokaryote homologous recombination-mediated gene editing, and facilitates rapid, accurate, one-pot, semi-quantitative nucleic acid diagnostics. In summary, the DR sequence mutation strategy provides simple, flexible, and diverse options for Cas12a activity regulation and functional optimization.

Nature CommunicationsVol. 16(1)
University of Science and Technology of China (CN), Fujian Medical University (CN), Union Hospital (CN)
National Natural Science Foundation of China, Natural Science Foundation of Anhui Province, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 3%
CRISPR and Genetic Engineering
6.45
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