Perk Enzo A, Laxalt Ana M, Cerrudo Ignacio
Instituto de Investigaciones Biológicas, CONICET-UNMdP, Mar del Plata, Argentina.
Bio Protoc. 2024 Jun 5;14(11):e5012. doi: 10.21769/BioProtoc.5012.
Gene editing technologies have revolutionized plant molecular biology, providing powerful tools for precise gene manipulation for understanding function and enhancing or modifying agronomically relevant traits. Among these technologies, the CRISPR-Cas9 system has emerged as a versatile and widely accepted strategy for targeted gene manipulation. This protocol provides detailed, step-by-step instructions for implementing CRISPR-Cas9 genome editing in tomato plants, with a specific focus in generating knockout lines for a target gene. For that, the guide RNA should preferentially be designed within the first exon downstream and closer to the start codon. The edited plants obtained are free of transgene cassette for expression of the CRISPR-Cas9 machinery. Key features • Two sgRNAs employed. • Takes 6-12 months to have an edited transgene-free plant. • Setup in tomato.
基因编辑技术彻底改变了植物分子生物学,为精确基因操作提供了强大工具,用于理解基因功能以及增强或改良与农艺相关的性状。在这些技术中,CRISPR-Cas9系统已成为一种通用且被广泛接受的靶向基因操作策略。本方案提供了在番茄植株中实施CRISPR-Cas9基因组编辑的详细、分步说明,特别着重于针对目标基因生成敲除系。为此,引导RNA应优先设计在第一个外显子下游且更靠近起始密码子的位置。所获得的编辑植株不含用于表达CRISPR-Cas9机制的转基因盒。关键特性 • 使用两个单向导RNA。 • 获得无转基因编辑植株需6至12个月。 • 在番茄中开展。