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CRISPR筛选在功能基因组学中的应用。

The applications of CRISPR screen in functional genomics.

作者信息

Qi Xiaolong, Zhang Jiwei, Zhao Yongzhao, Chen Tao, Xiang Yi, Hui Jialiang, Cai Danxian, Liu Yanna, Xia Lei, Yu Tao, Li Guoxin

出版信息

Brief Funct Genomics. 2017 Jan;16(1):34-37. doi: 10.1093/bfgp/elw020. Epub 2016 Jun 20.

Abstract

CRISPR technology has rapidly changed the face of biological research, such that precise genome editing has now become routine for many labs within several years of its initial development. CRISPR/Cas9 (Clustered Regularly Interspace Short Palindromic Repeat/CRISPR-associated nuclease 9) gene editing system is a powerful and groundbreaking programmable genome editing technology developed based on an adaptive bacterial and archaea immune system resisting the invasion of exogenous nucleic acid. Compared with traditional genome editing technology, CRISPR/Cas9 system is easier, efficient and less cytotoxic. CRISPR/Cas9 gene editing technology has been applied to many aspects of cancer research, including research on tumor genes, constructing animal tumor models, screening tumor phenotypic-related and resistance-associated gene and cancer gene therapy. In this review, we focus on the application of the CRISPR screen for this fast moving field. Finally, we discuss practical aspects of screen design, and outline a further step forward in the rapidly expanding field of genome editing.

摘要

CRISPR技术迅速改变了生物学研究的面貌,以至于在其最初开发后的几年内,精确的基因组编辑现已成为许多实验室的常规操作。CRISPR/Cas9(成簇规律间隔短回文重复序列/CRISPR相关核酸酶9)基因编辑系统是一种强大且具有开创性的可编程基因组编辑技术,它基于细菌和古菌抵御外源核酸入侵的适应性免疫系统而开发。与传统的基因组编辑技术相比,CRISPR/Cas9系统更简便、高效且细胞毒性更小。CRISPR/Cas9基因编辑技术已应用于癌症研究的许多方面,包括肿瘤基因研究、构建动物肿瘤模型、筛选肿瘤表型相关基因和耐药相关基因以及癌症基因治疗。在本综述中,我们重点关注CRISPR筛选在这个快速发展领域中的应用。最后,我们讨论筛选设计的实际问题,并概述在迅速扩展的基因组编辑领域中的进一步发展。

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