CRISPR-powered RNA sensing in vivo

被引:0
|
作者
Jiang, Guo [1 ,2 ]
Gao, Yuanli [1 ,2 ,3 ]
Zhou, Nan [1 ,2 ]
Wang, Baojun [1 ,2 ]
机构
[1] Zhejiang Univ, Coll Chem & Biol Engn, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, ZJU Hangzhou Global Sci & Technol Innovat Ctr, Hangzhou 311200, Zhejiang, Peoples R China
[3] Univ Edinburgh, Sch Biol Sci, Edinburgh EH9 3FF, Scotland
基金
国家重点研发计划;
关键词
CONDITIONAL GUIDE RNAS; NUCLEIC-ACID DETECTION; MESSENGER-RNA; PROTEIN CLEAVAGE; MAMMALIAN-CELLS; GENOMIC DNA; BACTERIAL; CLASSIFICATION; ENDONUCLEASE; CONNECTIONS;
D O I
10.1016/j.tibtech.2024.04.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
RNA sensing in vivo evaluates past or ongoing endogenous RNA disturbances, which is crucial for identifying cell types and states and diagnosing diseases. Recently, the CRISPR-driven genetic circuits have offered promising solutions to burgeoning challenges in RNA sensing. This review delves into the cuttingedge developments of CRISPR-powered RNA sensors in vivo, reclassifying these RNA sensors into four categories based on their working mechanisms, including programmable reassembly of split single-guide RNA (sgRNA), RNA-triggered RNA processing and protein cleavage, miRNA-triggered RNA interference (RNAi), and strand displacement reactions. Then, we discuss the advantages and challenges of existing methodologies in diverse application scenarios and anticipate and analyze obstacles and opportunities in forthcoming practical implementations.
引用
收藏
页码:1601 / 1614
页数:14
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