反式激活crRNA
清脆的
效应器
核糖核酸
核酸
生物
计算生物学
核苷酸
遗传学
回文
DNA
化学
Cas9
劈理(地质)
核酸结构
分子生物学
引导RNA
细胞生物学
核酶
小RNA
限制
生物化学
单核苷酸多态性
寡核苷酸
作者
Xin Qiao,Yanmin Gao,Jiaojiao Li,Zhaoguan Wang,Hongyan Qiao,Hao Qi
摘要
Abstract RNA‐guided CRISPR (RNA‐targeting clustered regularly interspaced short palindromic repeats) effector Cas13d is the smallest Class II subtype VI proteins identified so far. Here, two recently identified Cas13d effectors from Eubacterium siraeum (Es) and Ruminococcus sp . (Rsp) were characterized and applied for sensitive nucleic acid detection. We demonstrated that the special target triggered collateral cleavage of these two Cas13d orthologs could provide rapid target RNA detection in picomolar range and then the tolerance for mismatch between crRNA and target RNA was characterized as well. Finally, an additional single mismatch was introduced into crRNA to enhance the two Cas13d orthologs mediated detection of low variant allele fraction, 0.1% T790M. Overall, this study demonstrated that both EsCas13d and RspCas13d could robustly detect target RNA carrying special single‐nucleotide variation with high specificity and sensitivity, thereby providing newly qualified machinery in toolbox for efficient molecular diagnostics.
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