基于Cas12a的一锅SNP检测具有高精度。

Hong-Xia Zhang , Caixiang Zhang , Shuhan Lu , Xiaohan Tong , Kun Zhang , Hao Yin , Ying Zhang
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引用次数: 3

摘要

基于CRISPR-Cas12a的一锅检测系统已被用于核酸检测和诊断。然而,它对单核苷酸多态性(SNP)的区分不够敏感,这极大地限制了它的应用。为了克服这些限制,我们设计了一种对SNP具有增强敏感性的LbCas12a变体,命名为seCas12a(敏感性Cas12a)。基于SeCas12a的一锅SNP检测系统是一个多功能平台,可以使用规范和非规范PAM,并且几乎不受突变类型的限制来区分位于1至17位之间的SNP。使用截短的crRNA进一步提高了seCas12a的SNP特异性。从机理上讲,我们发现只有当顺式切割处于0.01min-1至0.0006min-1之间的低水平时,才能在一锅试验中获得良好的信噪比。应用基于SeCas12a的一锅SNP检测系统检测人类临床样本中的药物基因组SNPs。在两种不同SNPs中测试的13个供体中,seCas12a介导的一锅系统可以在30分钟内以100%的准确率忠实地检测SNPs。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Cas12a-based one-pot SNP detection with high accuracy

CRISPR-Cas12a based one-pot detection system has been used in nucleic acid detection and diagnosis. However, it is not sensitive enough to distinguish single nucleotide polymorphisms (SNP), which has greatly restricted its application. To overcome these limitations, we engineered a LbCas12a variant with enhanced sensitivity against SNP, named seCas12a (sensitive Cas12a). SeCas12a-based one-pot SNP detection system is a versatile platform that could use both canonical and non-canonical PAM, and was almost not limited by mutation types to distinguish SNPs located between position 1 to 17. The use of truncated crRNA further improved SNP specificity of seCas12a. Mechanistically, we found only when the cis-cleavage was at low level between 0.01min−1 and 0.0006 min−1, a good signal-to-noise ratio can be achieved in one-pot test. SeCas12a-based one-pot SNP detection system was applied to detect pharmacogenomic SNPs in human clinical samples. Of thirteen donors tested in two different SNPs, the seCas12a mediated one-pot system could faithfully detect the SNPs in 30 min with 100% accuracy.

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来源期刊
Cell insight
Cell insight Neuroscience (General), Biochemistry, Genetics and Molecular Biology (General), Cancer Research, Cell Biology
CiteScore
2.70
自引率
0.00%
发文量
0
审稿时长
35 days
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