Induction of targeted, heritable mutations in barley and Brassica oleracea using RNA-guided Cas9 nuclease

被引:325
|
作者
Lawrenson, Tom [1 ]
Shorinola, Oluwaseyi [1 ]
Stacey, Nicola [1 ]
Li, Chengdao [2 ]
Ostergaard, Lars [1 ]
Patron, Nicola [3 ]
Uauy, Cristobal [1 ]
Harwood, Wendy [1 ]
机构
[1] John Innes Ctr, Colney NR4 7UH, Herts, England
[2] Murdoch Univ, Western Barley Genet Alliance, Murdoch, WA 6150, Australia
[3] Sainsbury Lab, Colney NR4 7UH, Herts, England
来源
GENOME BIOLOGY | 2015年 / 16卷
基金
英国生物技术与生命科学研究理事会;
关键词
Genome editing; CRISPR/Cas9; Barley; Brassica; PM19; GA4; Crops; Mutations; Breeding; Off-target; CRISPR/CAS9; SYSTEM; GENOME MODIFICATION; POD SHATTER; ARABIDOPSIS; SPECIFICITY; DNA; GENERATION; MULTIPLEX; DELETIONS; GENES;
D O I
10.1186/s13059-015-0826-7
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
Background: The RNA-guided Cas9 system represents a flexible approach for genome editing in plants. This method can create specific mutations that knock-out or alter target gene function. It provides a valuable tool for plant research and offers opportunities for crop improvement. Results: We investigate the use and target specificity requirements of RNA-guided Cas9 genome editing in barley (Hordeum vulgare) and Brassica oleracea by targeting multicopy genes. In barley, we target two copies of HvPM19 and observe Cas9-induced mutations in the first generation of 23 % and 10 % of the lines, respectively. In B. oleracea, targeting of BolC. GA4. a leads to Cas9-induced mutations in 10 % of first generation plants screened. In addition, a phenotypic screen identifies T-0 plants with the expected dwarf phenotype associated with knock-out of the target gene. In both barley and B. oleracea stable Cas9-induced mutations are transmitted to T-2 plants independently of the T-DNA construct. We observe off-target activity in both species, despite the presence of at least one mismatch between the single guide RNA and the non-target gene sequences. In barley, a transgene-free plant has concurrent mutations in the target and non-target copies of HvPM19. Conclusions: We demonstrate the use of RNA-guided Cas9 to generate mutations in target genes of both barley and B. oleracea and show stable transmission of these mutations thus establishing the potential for rapid characterisation of gene function in these species. In addition, the off-target effects reported offer both potential difficulties and specific opportunities to target members of multigene families in crops.
引用
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页数:13
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