反式激活crRNA
清脆的
核酸酶
计算生物学
核糖核酸
化学
DNA
生物
基因组编辑
基因
生物化学
作者
Yong Chen,Yibin Zhang,Siyuan Luo,Xinyao Yang,Conghui Liu,Qianling Zhang,Yizhen Liu,Xueji Zhang
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2023-10-12
卷期号:95 (42): 15606-15613
被引量:13
标识
DOI:10.1021/acs.analchem.3c02687
摘要
The CRISPR/Cas13a system has promising applications in clinical small noncoding RNA (sncRNA) detection because it is free from the interference of genomic DNA. However, detecting ultrashort sncRNAs (less than 20 nucleotides) has been challenging because the Cas13a nuclease requires longer crRNA–target RNA hybrids to be activated. Here, we report the development of a foldback-crRNA-enhanced CRISPR/Cas13a (FCECas13a) system that overcomes the limitations of the current CRISPR/Cas13a system in detecting ultrashort sncRNAs. The FCECas13a system employs a 3′-terminal foldback crRNA that hybridizes with the target ultrashort sncRNA, forming a double strand that "tricks" the Cas13a nuclease into activating the HEPN structural domain and generating trans-cleavage activity. The FCECas13a system can accurately detect miRNA720 (a sncRNA currently known as tRNA-derived small RNA), which is only 17 nucleotides long and has a concentration as low as 15 fM within 20 min. This FCECas13a system opens new avenues for ultrashort sncRNA detection with significant implications for basic biological research, disease prognosis, and molecular diagnosis.
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