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使用CRISPR/Cas系统进行高效突变的策略。

Strategies for High-Efficiency Mutation Using the CRISPR/Cas System.

作者信息

Feng Shuying, Wang Zilong, Li Aifang, Xie Xin, Liu Junjie, Li Shuxuan, Li Yalan, Wang Baiyan, Hu Lina, Yang Lianhe, Guo Tao

机构信息

Medical College, Henan University of Chinese Medicine, Zhengzhou, China.

Department of Pharmacy, Henan University of Chinese Medicine, Zhengzhou, China.

出版信息

Front Cell Dev Biol. 2022 Feb 7;9:803252. doi: 10.3389/fcell.2021.803252. eCollection 2021.

Abstract

Clustered regularly interspaced short palindromic repeats (CRISPR)-associated systems have revolutionized traditional gene-editing tools and are a significant tool for ameliorating gene defects. Characterized by high target specificity, extraordinary efficiency, and cost-effectiveness, CRISPR/Cas systems have displayed tremendous potential for genetic manipulation in almost any organism and cell type. Despite their numerous advantages, however, CRISPR/Cas systems have some inherent limitations, such as off-target effects, unsatisfactory efficiency of delivery, and unwanted adverse effects, thereby resulting in a desire to explore approaches to address these issues. Strategies for improving the efficiency of CRISPR/Cas-induced mutations, such as reducing off-target effects, improving the design and modification of sgRNA, optimizing the editing time and the temperature, choice of delivery system, and enrichment of sgRNA, are comprehensively described in this review. Additionally, several newly emerging approaches, including the use of Cas variants, anti-CRISPR proteins, and mutant enrichment, are discussed in detail. Furthermore, the authors provide a deep analysis of the current challenges in the utilization of CRISPR/Cas systems and the future applications of CRISPR/Cas systems in various scenarios. This review not only serves as a reference for improving the maturity of CRISPR/Cas systems but also supplies practical guidance for expanding the applicability of this technology.

摘要

成簇规律间隔短回文重复序列(CRISPR)相关系统彻底改变了传统的基因编辑工具,是改善基因缺陷的重要工具。CRISPR/Cas系统具有高靶向特异性、非凡效率和成本效益等特点,在几乎任何生物体和细胞类型的基因操作中都显示出巨大潜力。然而,尽管CRISPR/Cas系统有诸多优点,但也存在一些固有局限性,如脱靶效应、递送效率不尽人意以及不良副作用,因此人们渴望探索解决这些问题的方法。本综述全面描述了提高CRISPR/Cas诱导突变效率的策略,如减少脱靶效应、改进sgRNA的设计和修饰、优化编辑时间和温度、选择递送系统以及富集sgRNA。此外,还详细讨论了几种新出现的方法,包括使用Cas变体、抗CRISPR蛋白和突变体富集。此外,作者对CRISPR/Cas系统应用中的当前挑战以及CRISPR/Cas系统在各种场景下的未来应用进行了深入分析。本综述不仅为提高CRISPR/Cas系统的成熟度提供了参考,也为扩大该技术的适用性提供了实用指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a918/8860194/e8936e6d9356/fcell-09-803252-g001.jpg

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