Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, OK, USA.
Methods Mol Biol. 2024;2832:281-290. doi: 10.1007/978-1-0716-3973-3_20.
CRISPR/Cas9 system is one of the most often utilized engineering tools for genome editing in many organisms including crop plants and presents great value in both basic and applied research. This is a preferred method because of its relative simplicity, cost-effectiveness, and reliability. The Cas9 nuclease guided by a short single guide RNA (gRNA) can generate double-strand DNA breaks (DSB) at the specific sites in chromosomal DNA. The DSB site is repaired by error-prone repair methods. During repair, some nucleotides are deleted or added at the target site. Here, we present a simplified protocol for generating mutants in gene of interest in rice using CRISPR/Cas9.
CRISPR/Cas9 系统是最常用于许多生物体(包括农作物)基因组编辑的工程工具之一,在基础研究和应用研究中都具有很高的价值。由于其相对简单、经济高效和可靠,这是一种首选方法。由短单链向导 RNA(gRNA)引导的 Cas9 核酸酶可在染色体 DNA 中的特定位点产生双链 DNA 断裂(DSB)。DSB 位点通过易错修复方法进行修复。在修复过程中,一些核苷酸在靶位点被缺失或添加。在这里,我们提供了一种简化的方案,用于使用 CRISPR/Cas9 在水稻中产生目的基因的突变体。