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CRISPR-Cas (clustered regularly interspaced short palindromic repeats (CRISP) and CRISPR associated proteins)系统是细菌用来防御病毒、质粒等外源核酸入侵的一种获得性免疫防御系统。随着研究的深入,CRISPR-Cas系统已发展为一种重要的基因编辑工具,并成功应用于动物、植物和微生物的基因改造中。但该基因编辑方法有时存在基因脱靶效应,从而限制了其推广应用。最近,通过将1种新发现的抗CRISPR蛋白(Anti-CRISPR protein,ACP)与CRISPR-Cas系统相结合,已成功开发出可控制基因脱靶效率的CRISPR-Cas基因编辑工具。本文首先对CRISPR-Cas系统及ACP进行了简要介绍,然后就CRISPR-Cas基因编辑工具及ACP在微生物基因改造的应用现状进行了综述,并对ACP介导的CRISPR-Cas基因编辑方法(ACP-CRISPR-Cas)在微生物基因编辑中的应用前景进行了讨论。  相似文献   
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陈学梅  魏云林  季秀玲 《遗传》2021,(3):240-248
噬菌体是地球上最多的生物实体,一直被认为是细菌的天敌。然而随着基因组学和分子生物学等技术的快速发展,人们发现噬菌体与宿主之间存在微妙而复杂的关系。前噬菌体是指溶原性细菌内存在的整套噬菌体DNA基因组,广泛分布在细菌基因组中,对调节细菌宿主生理具有重要作用,如参与调节宿主的毒力、影响生物膜形成、赋予宿主免疫力等。有趣的是,前噬菌体可以通过"监听"细菌的群体感应来调节自身的溶原–裂解状态。近年来,一些细菌中由前噬菌体编码的抗CRISPR蛋白的发现引起了人们对前噬菌体研究的关注。因此,对前噬菌体的研究可以为改造宿主和前噬菌体提供基础理论参考。本文对前噬菌体的预测、分布、分类及功能进行了综述,以期为进一步研究噬菌体与宿主间的关系提供基础。  相似文献   
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Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas (CRISPR-associated proteins) systems provide bacteria and archaea with an adaptive immune response against invasion by mobile genetic elements like phages, plasmids, and transposons. These systems have been repurposed as very powerful biotechnological tools for gene editing applications in both bacterial and eukaryotic systems. The discovery of natural off-switches for CRISPR-Cas systems, known as anti-CRISPR proteins, provided a mechanism for controlling CRISPR-Cas activity and opened avenues for the development of more precise editing tools. In this review, we focus on the inhibitory mechanisms of anti-CRISPRs that are active against type II CRISPR-Cas systems and briefly discuss their biotechnological applications.  相似文献   
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Mobile genetic elements (MGEs) such as bacteriophages and their host prokaryotes are trapped in an eternal battle against each other. To cope with foreign infection, bacteria and archaea have evolved multiple immune strategies, out of which CRISPR-Cas system is up to now the only discovered adaptive system in prokaryotes. Despite the fact that CRISPR-Cas system provides powerful and delicate protection against MGEs, MGEs have also evolved anti-CRISPR proteins (Acrs) to counteract the CRISPR-Cas immune defenses. To date, 46 families of Acrs targeting type I CRISPR-Cas system have been characterized, out of which structure information of 21 families have provided insights on their inhibition strategies. Here, we review the non-canonical inhibition strategies adopted by Acrs targeting type I CRISPR-Cas systems based on their structure information by incorporating the most recent advances in this field, and discuss our current understanding and future perspectives. The delicate interplay between type I CRISPR-Cas systems and their Acrs provides us with important insights into the ongoing fierce arms race between prokaryotic hosts and their predators.  相似文献   
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《Cell》2017,168(1-2):150-158.e10
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