Boubakri Hatem
Laboratory of Legumes and Sustainable Agrosystems, Centre of Biotechnology of Borj-Cedria, BP 901, 2050 Hammam-Lif, Tunisia.
Gene. 2023 May 25;866:147334. doi: 10.1016/j.gene.2023.147334. Epub 2023 Mar 4.
Nowadays, agricultural production is strongly affected by both climate change and pathogen attacks which seriously threaten global food security. For a long time, researchers have been waiting for a tool allowing DNA/RNA manipulation to tailor genes and their expression. Some earlier genetic manipulation methods such as meganucleases (MNs), zinc finger nucleases (ZFNs), transcription activator-like effector nucleases (TALENs) allowed site directed modification but their successful rate was limited due to lack of flexibility when targeting a 'site-specific nucleic acid'. The discovery of clustered regularly interspaced short palindrome repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) system has revolutionized genome editing domain in different living organisms during the past 9 years. Based on RNA-guided DNA/RNA recognition, CRISPR/Cas9 optimizations have offered an unrecorded scientific opportunity to engineer plants resistant to diverse pathogens. In this report, we describe the main characteristics of the primary reported-genome editing tools ((MNs, ZFNs, TALENs) and evaluate the different CRISPR/Cas9 methods and achievements in developing crop plants resistant to viruses, fungi and bacteria.
如今,农业生产受到气候变化和病原体侵袭的严重影响,这对全球粮食安全构成了严重威胁。长期以来,研究人员一直在期待一种能够进行DNA/RNA操作以定制基因及其表达的工具。一些早期的基因操作方法,如巨核酸酶(MNs)、锌指核酸酶(ZFNs)、转录激活样效应物核酸酶(TALENs),能够实现定点修饰,但由于在靶向“位点特异性核酸”时缺乏灵活性,其成功率有限。在过去9年中,成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关蛋白9(Cas9)系统的发现彻底改变了不同生物体中的基因组编辑领域。基于RNA引导的DNA/RNA识别,CRISPR/Cas9的优化为培育抗多种病原体的植物提供了前所未有的科学机遇。在本报告中,我们描述了最初报道的基因组编辑工具(MNs、ZFNs、TALENs)的主要特点,并评估了不同的CRISPR/Cas9方法以及在培育抗病毒、真菌和细菌的作物方面所取得的成果。