基于CRISPR的基因编辑技术及其在微生物工程中的应用

Junwei Wei, Yingjun Li
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引用次数: 1

摘要

基因编辑技术涉及对特定靶基因进行修饰以获得新的功能或表型。簇状规则间隔短回文重复序列(CRISPR)-Cas介导的技术的最新进展为细胞和生物体的基因工程提供了一种有效的工具。在这里,我们回顾了三种新兴的基因编辑工具(ZFNs、TALENs和CRISPR-Cas),并简要介绍了CRISPR-Cas系统的原理、分类和机制。详细描述了基于内源性和外源性CRISPR-Cas系统的基因编辑策略,以及新型碱基编辑器(BE)、引物编辑器(PE)和CRISPR相关转座酶(CAST)技术。此外,我们还总结了基于CRISPR的基因编辑工具在工业微生物和益生菌修饰中的应用进展。最后,讨论了基于CRISPR的基因编辑工具的潜在挑战和未来前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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CRISPR-based gene editing technology and its application in microbial engineering

Gene editing technology involves the modification of a specific target gene to obtain a new function or phenotype. Recent advances in clustered regularly interspaced short palindromic repeats (CRISPR)-Cas-mediated technologies have provided an efficient tool for genetic engineering of cells and organisms. Here, we review the three emerging gene editing tools (ZFNs, TALENs, and CRISPR-Cas) and briefly introduce the principle, classification, and mechanisms of the CRISPR-Cas systems. Strategies for gene editing based on endogenous and exogenous CRISPR-Cas systems, as well as the novel base editor (BE), prime editor (PE), and CRISPR-associated transposase (CAST) technologies, are described in detail. In addition, we summarize recent developments in the application of CRISPR-based gene editing tools for industrial microorganism and probiotics modifications. Finally, the potential challenges and future perspectives of CRISPR-based gene editing tools are discussed.

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