清脆的
核酸
DNA
核糖核酸
计算生物学
核酸内切酶
生物
基因组编辑
分子生物学
遗传学
基因
作者
Charly Mayran,Steven J. Henry,Elena Pinchon,Chantal Fournier‐Wirth,Jean François Cantaloube,Vincent Foulongne
出处
期刊:Virologie
[John Libbey Eurotext]
日期:2022-07-01
卷期号:26 (4): 303-313
标识
DOI:10.1684/vir.2022.0966
摘要
CRISPR-Cas is an adaptive immune system that prevents bacteria and archea from nucleic acids invasion such as viral genomes. The ability of the CRISPR-Cas technology to effectively and precisely cut a targeted genomic DNA region was exploited to develop powerful genome editing tools that were adapted for a wide range of applications, revolutionizing biological sciences. The CRISPR-Cas system consists of a Cas endonuclease triggered by a RNA guide for highly specific cleavage of targeted DNA or RNA sequences. In addition to the target specific cleavage, some Cas enzymes, including Cas12a and Cas13a, display a collateral trans-cleavage activity that allows the cleavage of all surrounding single-stranded nucleic acids. These biosensing activities of CRISPR-Cas systems, based on target specific binding and cleavage, are promising tools to develop accurate diagnostic methods to detect specific nucleic acids. CRISPRCas could therefore be used to diagnose a wide variety of diseases. In the current review we propose to describe the more significant advances for virus detection based on CRISPR-Cas systems.
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