John Innes Centre, Department of Crop Genetics, Norwich Research Park, Norwich, United Kingdom.
Curr Protoc. 2021 Mar;1(3):e65. doi: 10.1002/cpz1.65.
The development and application of high precision genome editing tools such as programmable nucleases are set to revolutionize crop breeding and are already having a major impact on fundamental science. Clustered regularly interspaced short palindromic repeats (CRISPR), and its CRISPR-associated protein (Cas), is a programmable RNA-guided nuclease enabling targeted site-specific double stranded breaks in DNA which, when incorrectly repaired, result in gene knockout. The two most widely cultivated wheat types are the tetraploid durum wheat (Triticum turgidum ssp. durum L.) and the hexaploid bread wheat (Triticum aestivum L.). Both species have large genomes, as a consequence of ancient hybridization events between ancestral progenitors. The highly conserved gene sequence and structure of homoeologs among subgenomes in wheat often permits their simultaneous targeting using CRISPR-Cas9 with single or paired single guide RNA (sgRNA). Since its first successful deployment in wheat, CRISPR-Cas9 technology has been applied to a wide array of gene targets of agronomical and scientific importance. The following protocols describe an experimentally derived strategy for implementing CRISRP-Cas9 genome editing, including sgRNA design, Golden Gate construct assembly, and screening analysis for genome edits. © 2021 The Authors. Basic Protocol 1: Selection of sgRNA target sequence for CRISPR-Cas9 Basic Protocol 2: Construct assembly using Golden Gate (MoClo) assembly Basic Protocol 3: Screening for CRISPR-Cas9 genome edits Alternate Protocol: BigDye Terminator reactions for screening of CRISPR-Cas9 genome edits.
高通量基因组编辑工具,如可编程核酸酶的发展和应用有望彻底改变作物的培育方式,并且已经对基础科学产生了重大影响。CRISPR(成簇的规律间隔的短回文重复序列)及其 CRISPR 相关蛋白(Cas)是一种可编程的 RNA 引导的核酸内切酶,能够在 DNA 中靶向特定的双链断裂,如果修复不正确,会导致基因敲除。两种最广泛种植的小麦类型是四倍体硬粒小麦(Triticum turgidum ssp. durum L.)和六倍体面包小麦(Triticum aestivum L.)。由于远古时期的祖先杂交事件,这两个物种都具有较大的基因组。小麦亚基因组之间同源基因序列和结构高度保守,通常可以使用 CRISPR-Cas9 与单个或成对的单指导 RNA(sgRNA)同时靶向它们。自首次在小麦中成功应用以来,CRISPR-Cas9 技术已被广泛应用于许多具有农业和科学重要性的基因靶标。以下方案描述了一种从实验中得出的实施 CRISPR-Cas9 基因组编辑的策略,包括 sgRNA 设计、Golden Gate 构建组装和基因组编辑的筛选分析。© 2021 作者。基础方案 1:CRISPR-Cas9 的 sgRNA 靶序列选择基础方案 2:使用 Golden Gate(MoClo)组装进行构建组装基础方案 3:CRISPR-Cas9 基因组编辑的筛选替代方案:用于筛选 CRISPR-Cas9 基因组编辑的 BigDye Terminator 反应。