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  3. Master Program in Global Agriculture Technology and Genomic Science (Global ATGS) / 全球農業科技與基因體科學碩士學位學程
  4. Simultaneous induction of mutant alleles of two allergenic genes in soybean by using site-directed mutagenesis
 
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Simultaneous induction of mutant alleles of two allergenic genes in soybean by using site-directed mutagenesis

Journal
BMC Plant Biology
Journal Volume
20
Journal Issue
1
Date Issued
2020-12-01
Author(s)
Sugano, Shota
Hirose, Aya
Kanazashi, Yuhei
Adachi, Kohei
Hibara, Miki
TAKESHI ITOH  
Mikami, Masafumi
Endo, Masaki
Hirose, Sakiko
Maruyama, Nobuyuki
Abe, Jun
Yamada, Tetsuya
DOI
10.1186/s12870-020-02708-6
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85095848364&doi=10.1186%2fs12870-020-02708-6&partnerID=40&md5=0f2edbbf7c990f05b268c585bc54739b
https://scholars.lib.ntu.edu.tw/handle/123456789/639060
URL
https://api.elsevier.com/content/abstract/scopus_id/85095848364
Abstract
Background: Soybean (Glycine max) is a major protein crop, because soybean protein has an amino acid score comparable to that of beef and egg white. However, many allergens have been identified among soybean proteins. A decrease in allergenic protein levels would be useful for expanding the market for soybean proteins and processed foods. Recently, the CRISPR/Cas9 system has been adopted as a powerful tool for the site-directed mutagenesis in higher plants. This system is expected to generate hypoallergenic soybean varieties. Results: We used two guide RNAs (gRNAs) and Agrobacterium-mediated transformation for simultaneous site-directed mutagenesis of two genes encoding the major allergens Gly m Bd 28 K and Gly m Bd 30 K in two Japanese soybean varieties, Enrei and Kariyutaka. We obtained two independent T0 Enrei plants and nine T0 Kariyutaka plants. Cleaved amplified polymorphic sequence (CAPS) analysis revealed that mutations were induced in both targeted loci of both soybean varieties. Sequencing analysis showed that deletions were the predominant mutation type in the targeted loci. The Cas9-free plants carrying the mutant alleles of the targeted loci with the transgenes excluded by genetic segregation were obtained in the T2 and T3 generations. Variable mutational spectra were observed in the targeted loci even in T2 and T3 progenies of the same T0 plant. Induction of multiple mutant alleles resulted in six haplotypes in the Cas9-free mutants derived from one T0 plant. Immunoblot analysis revealed that no Gly m Bd 28 K or Gly m Bd 30 K protein accumulated in the seeds of the Cas9-free plants. Whole-genome sequencing confirmed that a Cas9-free mutant had also no the other foreign DNA from the binary vector. Our results demonstrate the applicability of the CRISPR/Cas9 system for the production of hypoallergenic soybean plants. Conclusions: Simultaneous site-directed mutagenesis by the CRISPR/Cas9 system removed two major allergenic proteins from mature soybean seeds. This system enables rapid and efficient modification of seed components in soybean varieties.
Subjects
CRISPR/Cas9 | Gly m Bd 28 K | Gly m Bd 30 K | Glycine max | Hypoallergenic soybean
Type
journal article

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