一种新型双导向CRISPR–Cas13策略提高单核苷酸变异检测特异性

📄 原文题目

A novel Dual-guide CRISPR–Cas13 strategy improves specificity for single-nucleotide variant detection

🔗 原文链接

https://academic.oup.com/nar/article/doi/10.1093/nar/gkag161/8500551?rss=1

💡 AI 核心解读

📝 英文原版摘要

<div class="boxTitle">Abstract</div>The emergence of CRISPR–Cas systems has transformed nucleic acid detection and manipulation. Cas13, a type VI CRISPR effector, targets RNA with high sensitivity through both cis (target RNA) and trans (collateral RNA) cleavage. This property enables the use of fluorescent reporters for sensitive diagnostics. However, Cas13’s heightened sensitivity also leads to reduced specificity due to its susceptibility to single-nucleotide mismatches, potentially causing off-target effects. To overcome this limitation, we developed the first Dual-guide RNA system for Cas13 that improves mismatch discrimination and enhances target specificity. This system employs two distinct RNAs—dcrRNA and dtracrRNA—which cooperatively recognize the target and reduce off-target activity. In vitro experiments demonstrated robust cis- and trans-RNase activity, indicating efficient and specific cleavage. The system accurately detected SARS-CoV-2 RNA, distinguished KRAS G12D and G12C mutations, and differentiated mucocutaneous from cutaneous Leishmania sequences in analytical assays, with clinical validation confirming accurate detection of positive and negative samples. These results highlight the Dual-guide Cas13 platform’s potential for precise, rapid, and reliable RNA detection. Overall, this approach represents a substantial advance over conventional Cas13 systems, offering improved specificity while maintaining clinically relevant sensitivity, and provides a generalizable tool for next-gen

eration molecular diagnostics and precision RNA targeting and regulation.