CRISPR-Cas9-mediated genome editing in apple and grapevine

被引：154

作者：

Osakabe, Yuriko ^{[1
]}

Liang, Zhenchang ^{[2
]}

Ren, Chong ^{[2
]}

Nishitani, Chikako ^{[3
]}

Osakabe, Keishi ^{[1
]}

Wada, Masato ^{[4
]}

Komori, Sadao ^{[5
]}

Malnoy, Mickael ^{[6
]}

Velasco, Riccardo ^{[6
,10
]}

Poli, Michele ^{[7
]}

Jung, Min-Hee ^{[8
]}

Koo, Ok-Jae ^{[7
,8
]}

Viola, Roberto ^{[9
]}

Kanchiswamy, Chidananda Nagamangala ^{[6
,7
]}

机构：

[1] Tokushima Univ, Fac Biosci & Bioind, Tokushima, Tokushima, Japan

[2] Chinese Acad Sci, Beijing Key Lab Grape Sci & Enol, Inst Bot, Key Lab Plant Resources, Beijing, Peoples R China

[3] NARO Inst Fruit Tree & Tea Sci, Div Fruit Breeding & Genet, Tsukuba, Ibaraki, Japan

[4] NARO Inst Fruit Tree & Tea Sci, Div Apple Res, Morioka, Iwate, Japan

[5] Iwate Univ, Fac Agr, Morioka, Iwate, Japan

[6] FEM, Genom & Biol Fruit Crop Dept, Res & Innovat Ctr, San Michele All Adige, TN, Italy

[7] PLANTeDIT Pvt Ltd, Cork, Ireland

[8] ToolGen, Seoul, South Korea

[9] Italian Inst Technol, Genoa, Italy

[10] CREA, Res Ctr Viticulture & Enol, Conegliano, TV, Italy

来源：

NATURE PROTOCOLS | 2018年 / 13卷 / 12期

关键词：

LEAF MESOPHYLL PROTOPLASTS; SOMATIC EMBRYOGENESIS; PLANT-REGENERATION; GENETIC-TRANSFORMATION; TARGETED MUTAGENESIS; HUMAN-CELLS; DNA; CRISPR/CAS9; DELIVERY; SYSTEM;

D O I：

10.1038/s41596-018-0067-9

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

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.

引用

页码：2844 / 2863

页数：20

共 43 条

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