| Literature DB >> 30390050 |
Yuriko Osakabe1, Zhenchang Liang2, Chong Ren2, Chikako Nishitani3, Keishi Osakabe4, Masato Wada5, Sadao Komori6, Mickael Malnoy7, Riccardo Velasco7,8, Michele Poli9, Min-Hee Jung10, Ok-Jae Koo9,10, Roberto Viola11, Chidananda Nagamangala Kanchiswamy12,13.
Abstract
The CRISPR-Cas9 genome-editing tool and the availability of whole-genome sequences from plant species have revolutionized our ability to introduce targeted mutations into important crop plants, both to explore genetic changes and to introduce new functionalities. Here, we describe protocols adapting the CRISPR-Cas9 system to apple and grapevine plants, using both plasmid-mediated genome editing and the direct delivery of CRISPR-Cas9 ribonucleoproteins (RNPs) to achieve efficient DNA-free targeted mutations in apple and grapevine protoplasts. We provide a stepwise protocol for the design and transfer of CRISPR-Cas9 components to apple and grapevine protoplasts, followed by verification of highly efficient targeted mutagenesis, and regeneration of plants following the plasmid-mediated delivery of components. Our plasmid-mediated procedure and the direct delivery of CRISPR-Cas9 RNPs can both be utilized to modulate traits of interest with high accuracy and efficiency in apple and grapevine, and could be extended to other crop species. The complete protocol employing the direct delivery of CRISPR-Cas9 RNPs takes as little as 2-3 weeks, whereas the plasmid-mediated procedure takes >3 months to regenerate plants and study the mutations.Entities:
Mesh:
Year: 2018 PMID: 30390050 DOI: 10.1038/s41596-018-0067-9
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491