State Key Laboratory of Plant Cell and Chromosome Engineering, and Center for Genome Editing, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
University of Chinese Academy of Sciences, Beijing, China.
Nat Protoc. 2018 Mar;13(3):413-430. doi: 10.1038/nprot.2017.145. Epub 2018 Feb 1.
This protocol is an extension to: Nat. Protoc. 9, 2395-2410 (2014); doi:10.1038/nprot.2014.157; published online 18 September 2014In recent years, CRISPR/Cas9 has emerged as a powerful tool for improving crop traits. Conventional plant genome editing mainly relies on plasmid-carrying cassettes delivered by Agrobacterium or particle bombardment. Here, we describe DNA-free editing of bread wheat by delivering in vitro transcripts (IVTs) or ribonucleoprotein complexes (RNPs) of CRISPR/Cas9 by particle bombardment. This protocol serves as an extension of our previously published protocol on genome editing in bread wheat using CRISPR/Cas9 plasmids delivered by particle bombardment. The methods we describe not only eliminate random integration of CRISPR/Cas9 into genomic DNA, but also reduce off-target effects. In this protocol extension article, we present detailed protocols for preparation of IVTs and RNPs; validation by PCR/restriction enzyme (RE) and next-generation sequencing; delivery by biolistics; and recovery of mutants and identification of mutants by pooling methods and Sanger sequencing. To use these protocols, researchers should have basic skills and experience in molecular biology and biolistic transformation. By using these protocols, plants edited without the use of any foreign DNA can be generated and identified within 9-11 weeks.
Nat. Protoc. 9, 2395-2410 (2014); doi:10.1038/nprot.2014.157; published online 18 September 2014。近年来,CRISPR/Cas9 技术已成为改良作物性状的强大工具。传统的植物基因组编辑主要依赖于农杆菌携带的质粒载体或粒子轰击。在此,我们通过粒子轰击递送体外转录物(IVT)或 CRISPR/Cas9 的核糖核蛋白复合物(RNP),描述了免质粒编辑面包小麦的方法。本方案是我们之前发表的使用通过粒子轰击递送的 CRISPR/Cas9 质粒编辑面包小麦基因组的方案的扩展。我们描述的方法不仅消除了 CRISPR/Cas9 随机整合到基因组 DNA 中,而且还减少了脱靶效应。在本方案扩展文章中,我们提供了详细的体外转录物和核糖核蛋白复合物制备方案;通过 PCR/限制性内切酶(RE)和下一代测序验证;通过生物弹道学进行递送;以及通过汇集方法和 Sanger 测序进行突变体的回收和鉴定。要使用这些方案,研究人员应具备分子生物学和生物弹道学的基本技能和经验。通过使用这些方案,可在 9-11 周内生成和鉴定无需使用任何外源 DNA 编辑的植物。