反式激活crRNA
清脆的
化学
核酸
计算生物学
小RNA
核糖核酸
滚动圆复制
抄写(语言学)
Cas9
纳米技术
DNA
生物
基因
生物化学
聚合酶
语言学
哲学
材料科学
作者
Gaoting Wang,Weimin Tian,Xiaoling Liu,Wei Ren,Chenghui Liu
标识
DOI:10.1021/acs.analchem.0c00680
摘要
Current CRISPR-Cas-based nucleic acid sensing methods relying on the preassembled Cas-crRNA complexes are generally limited to the detection of protospacer-adjacent motif (PAM)-containing sequences, and nonspecific backgrounds are inevitable. Herein, we propose a new CRISPR-derived microRNA sensing mechanism based on rolling circle transcription (RCT)-unleashed self-recruiting of crRNA by Cas12a (Cas12a-SCR). In Cas12a-SCR, target microRNA can specifically trigger RCT to produce a long single-strand RNA with numerous pre-crRNA repeats, which can be trimmed and recruited by Cas12a actively. This new target-initiated, real-time producing, trimming, and self-assembling manner of Cas12a-crRNA remarkably suppresses the nonspecific background and relieves the stringent requirement of PAM site in the target sequence. Thus, the universality of the Cas12a-SCR toward different nucleic acid sequences is greatly expanded.
科研通智能强力驱动
Strongly Powered by AbleSci AI