反式激活crRNA
工具箱
清脆的
计算机科学
计算生物学
灵活性(工程)
基因组编辑
互补性(分子生物学)
合成生物学
生物
基因表达调控
基因组工程
假结
作者
Jing Han,Min Yuan,Lan Hu,Jie‐Jie Chen,Shuxia Zhang,Xiaofan Li,Zhou‐Hua Cheng,Dong‐Feng Liu,Han‐Qing Yu
标识
DOI:10.1038/s41467-025-64010-z
摘要
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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