Journal
NATURE PROTOCOLS
Volume 13, Issue 3, Pages 413-430Publisher
NATURE PORTFOLIO
DOI: 10.1038/nprot.2017.145
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Funding
- National Natural Science Foundation of China [31788103, 31420103912, 31570369]
- Chinese Academy of Sciences [QYZDY-SSW-SMC030, GJHZ1602]
- National Transgenic Science and Technology Program [2016ZX08010-002]
- National Key Research and Development Program of China [2016YFD0101804]
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In recent years, CRISPR/Cas9 has emerged as a powerful tool for improving crop traits. Conventional plant genome editing mainly relies on ptasmid-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.
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