Generation of a multiplex mutagenesis population via pooled CRISPR-Cas9 in soya bean

被引:149
作者
Bai, Mengyan [1 ]
Yuan, Juehui [1 ]
Kuang, Huaqin [2 ]
Gong, Pingping [2 ]
Li, Suning [2 ,3 ]
Zhang, Zhihui [1 ,2 ]
Liu, Bo [1 ,2 ]
Sun, Jiafeng [1 ,2 ]
Yang, Maoxiang [1 ,2 ]
Yang, Lan [4 ]
Wang, Dong [4 ]
Song, Shikui [2 ]
Guan, Yuefeng [2 ]
机构
[1] Fujian Agr & Forestry Univ, Coll Resources & Environm, Fujian Prov Key Lab Haixia Appl Plant Syst Biol, Fuzhou, Fujian, Peoples R China
[2] Fujian Agr & Forestry Univ, Haixia Inst Sci & Technol, FAFU UCR Joint Ctr Hort Biol & Metabol, Fuzhou, Fujian, Peoples R China
[3] Fujian Agr & Forestry Univ, Coll Life Sci, Fuzhou, Fujian, Peoples R China
[4] Nanchang Univ, Key Lab Mol Biol & Gene Engn Jiangxi Prov, Coll Life Sci, Nanchang, Jiangxi, Peoples R China
基金
美国国家科学基金会;
关键词
CRISPR-Cas9; soya bean; multiplex mutagenesis; CRISPR population; nodulation; TARGETED MUTAGENESIS; GLYCINE-MAX; MEDICAGO-TRUNCATULA; GENOME; CRISPR/CAS9; NUCLEASES; SEQUENCE; TALENS; ROOTS; GENES;
D O I
10.1111/pbi.13239
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The output of genetic mutant screenings in soya bean [Glycine max (L.) Merr.] has been limited by its paleopolypoid genome. CRISPR-Cas9 can generate multiplex mutants in crops with complex genomes. Nevertheless, the transformation efficiency of soya bean remains low and, hence, remains the major obstacle in the application of CRISPR-Cas9 as a mutant screening tool. Here, we report a pooled CRISPR-Cas9 platform to generate soya bean multiplex mutagenesis populations. We optimized the key steps in the screening protocol, including vector construction, sgRNA assessment, pooled transformation, sgRNA identification and gene editing verification. We constructed 70 CRISPR-Cas9 vectors to target 102 candidate genes and their paralogs which were subjected to pooled transformation in 16 batches. A population consisting of 407 T0 lines was obtained containing all sgRNAs at an average mutagenesis frequency of 59.2%, including 35.6% lines carrying multiplex mutations. The mutation frequency in the T1 progeny could be increased further despite obtaining a transgenic chimera. In this population, we characterized gmric1/gmric2 double mutants with increased nodule numbers and gmrdn1-1/1-2/1-3 triple mutant lines with decreased nodulation. Our study provides an advanced strategy for the generation of a targeted multiplex mutant population to overcome the gene redundancy problem in soya bean as well as in other major crops.
引用
收藏
页码:721 / 731
页数:11
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