Borrelli Virginia M G, Brambilla Vittoria, Rogowsky Peter, Marocco Adriano, Lanubile Alessandra
Department of Sustainable Crop Production, Università Cattolica del Sacro Cuore, Piacenza, Italy.
Department of Agricultural and Environmental Sciences - Production, Territory, Agroenergy, University of Milan, Milan, Italy.
Front Plant Sci. 2018 Aug 24;9:1245. doi: 10.3389/fpls.2018.01245. eCollection 2018.
Genome editing technologies have progressed rapidly and become one of the most important genetic tools in the implementation of pathogen resistance in plants. Recent years have witnessed the emergence of site directed modification methods using meganucleases, zinc finger nucleases (ZFNs), transcription activator-like effector nucleases (TALENs), and clustered regularly interspaced short palindrome repeats (CRISPR)/CRISPR-associated protein 9 (Cas9). Recently, CRISPR/Cas9 has largely overtaken the other genome editing technologies due to the fact that it is easier to design and implement, has a higher success rate, and is more versatile and less expensive. This review focuses on the recent advances in plant protection using CRISPR/Cas9 technology in model plants and crops in response to viral, fungal and bacterial diseases. As regards the achievement of viral disease resistance, the main strategies employed in model species such as and , which include the integration of CRISPR-encoding sequences that target and interfere with the viral genome and the induction of a CRISPR-mediated targeted mutation in the host plant genome, will be discussed. Furthermore, as regards fungal and bacterial disease resistance, the strategies based on CRISPR/Cas9 targeted modification of susceptibility genes in crop species such as rice, tomato, wheat, and citrus will be reviewed. After spending years deciphering and reading genomes, researchers are now editing and rewriting them to develop crop plants resistant to specific pests and pathogens.
基因组编辑技术发展迅速,已成为植物中实现病原体抗性的最重要的遗传工具之一。近年来,出现了使用巨型核酸酶、锌指核酸酶(ZFNs)、转录激活样效应因子核酸酶(TALENs)以及成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关蛋白9(Cas9)的定点修饰方法。最近,CRISPR/Cas9在很大程度上超越了其他基因组编辑技术,因为它更易于设计和实施,成功率更高,用途更广且成本更低。本综述重点关注利用CRISPR/Cas9技术在模式植物和作物中应对病毒、真菌和细菌病害实现植物保护方面的最新进展。关于实现病毒病抗性,将讨论在拟南芥和烟草等模式物种中采用的主要策略,包括整合靶向并干扰病毒基因组的CRISPR编码序列以及在宿主植物基因组中诱导CRISPR介导的靶向突变。此外,关于真菌和细菌病害抗性,将综述基于CRISPR/Cas9对水稻、番茄、小麦和柑橘等作物物种中的感病基因进行靶向修饰的策略。在花费数年时间解读和读取基因组之后,研究人员现在正在编辑和改写它们,以培育对特定害虫和病原体具有抗性的作物。