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Biotechnol Adv. 2015 Jan-Feb;33(1):41-52. doi: 10.1016/j.biotechadv.2014.12.006. Epub 2014 Dec 20.

The CRISPR/Cas9 system for plant genome editing and beyond.

Author information

1
Institute for Molecular Biotechnology, RWTH Aachen University, Aachen, Germany. Electronic address: luisa.bortesi@molbiotech.rwth-aachen.de.
2
Institute for Molecular Biotechnology, RWTH Aachen University, Aachen, Germany; Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Aachen, Germany.

Abstract

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.

KEYWORDS:

CRISPR; Cas9; Gene targeting; Genome editing; Plants; Site-specific nuclease; Targeted mutagenesis

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