Research and Application of the Engineered gRNA Technology in the CRISPR/Cas System
10.13865/j.cnki.cjbmb.2024.06.1027
- VernacularTitle:CRISPR/Cas系统中工程化gRNA技术的研究和应用
- Author:
Liu TAN
1
;
Bang-Ce YE
;
Bin-Cheng YIN
Author Information
1. 浙江工业大学药学院,长三角绿色制药协同创新中心,杭州 310014
- Keywords:
clustered regularly interspaced short palindromic repeats(CRISPR)/CRISPR-associated(Cas)system;
gRNA engineering;
genome editing;
specificity
- From:
Chinese Journal of Biochemistry and Molecular Biology
2024;40(8):1078-1092
- CountryChina
- Language:Chinese
-
Abstract:
The CRISPR/Cas is an immune defense system acquired by prokaryotes to resist the invasion of foreign genetic materials during their evolutionary process.In recent years,it has been developed into an efficient tool for genome editing,gene regulation and molecular diagnosis.Its programmable targeting mechanism has opened the door to use this system for genome manipulation and allows for dynamic regu-lation and control of gene expression within its activity range.As one of the most flexible and cost-effec-tive techniques among existing gene modification methods,it has been widely applied in clinical disease treatment,industrial and agricultural production,sustainable dye development,chemical processing and many other fields.With the continuous investigation and exploration of the CRISPR/Cas system,a large number of studies have been reported on the engineering modification and optimization approaches of gRNA,including changing the length of the spacer region,regulating the structure of constant and varia-ble sequence parts,adding extra functional sequences through the end or middle extension,and chemical synthesis modifications,in order to reduce off-target and mutation rates,improve the efficiency of the CRISPR system,and fully stimulate the potential of CRISPR gene manipulation tools in biomedical fields.Based on this,this review will introduce the latest progress in gRNA engineering design strategies and application research of CRISPR/Cas9 and CRISPR/Cas12 systems,analyze and discuss the opportu-nities and challenges in the current gRNA engineering technology,aiming to provide ideas and reference directions for obtaining gRNAs with better performance,thereby effectively improving the ability to probe the human genomes using the CRISPR/Cas system and bringing more possibilities to programmable biology.
