The CRISPR/Cas9 system for plant genome editing and beyond

被引:692
|
作者
Bortesi, Luisa [1 ]
Fischer, Rainer [1 ,2 ]
机构
[1] Rhein Westfal TH Aachen, Inst Mol Biotechnol, D-52074 Aachen, Germany
[2] Fraunhofer Inst Mol Biol & Appl Ecol IME, Aachen, Germany
基金
欧洲研究理事会;
关键词
CRISPR; Cas9; Site-specific nuclease; Genome editing; Targeted mutagenesis; Gene targeting; Plants; ZINC-FINGER NUCLEASES; DOUBLE-STRAND BREAKS; TARGETED MUTAGENESIS; HUMAN-CELLS; GUIDE RNA; ANALYSIS REVEALS; RATIONAL DESIGN; GENE-TRANSFER; DNA CLEAVAGE; IN-VIVO;
D O I
10.1016/j.biotechadv.2014.12.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Targeted genome editing using artificial nucleases has the potential to accelerate basic research as well as plant breeding by providing the means to modify genomes rapidly in a precise and predictable manner. Here we describe the clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated protein 9 (Cas9) system, a recently developed tool for the introduction of site-specific double-stranded DNA breaks. We highlight the strengths and weaknesses of this technology compared with two well-established genome editing platforms: zinc finger nucleases (ZFNs) and transcription activator-like effector nucleases (TALENs). We summarize recent results obtained in plants using CRISPR/Cas9 technology, discuss possible applications in plant breeding and consider potential future developments. (C) 2015 Elsevier Inc.
引用
收藏
页码:41 / 52
页数:12
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