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[用于CRISPR基因组编辑的新一代工具:CRISPR/Cpf1]

[The new generation tool for CRISPR genome editing: CRISPR/Cpf1].

作者信息

Yang Fan, Li Yin

机构信息

CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2017 Mar 25;33(3):361-371. doi: 10.13345/j.cjb.170029.

Abstract

Almost all archaea and many bacteria achieve adaptive immunity through a diverse set of CRISPR-Cas systems. From 2012, Cas9 has been harnessed by thousands of laboratories for genome editing applications in a variety of experimental model systems. Cas9 is driving innovative applications from basic biology to biotechnology and medicine. However, numerous challenges still remain, such as limited targeting range, toxicity, and potential for off-target mutagenesis. Cpf1 represents a class 2/type V CRISPR RNA-guided endonuclease that is distinct from the type II CRISPR Cas9 nuclease. Future exploration of strategies using Cpf1 is expected to bring solutions for some of the biggest challenges facing genome editing. Here, we review the development and applications of Cpf1 for a variety of research or applications, and highlight challenges as well as future directions.

摘要

几乎所有古菌和许多细菌都通过多种CRISPR-Cas系统实现适应性免疫。自2012年以来,数千个实验室已利用Cas9在各种实验模型系统中进行基因组编辑应用。Cas9正在推动从基础生物学到生物技术和医学的创新应用。然而,仍然存在许多挑战,例如靶向范围有限、毒性以及脱靶诱变的可能性。Cpf1是一种2类/V型CRISPR RNA引导的核酸内切酶,与II型CRISPR Cas9核酸酶不同。预计未来对使用Cpf1的策略的探索将为基因组编辑面临的一些最大挑战带来解决方案。在这里,我们综述了Cpf1在各种研究或应用中的发展和应用,并强调了挑战以及未来的方向。

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