Abstract

BackgroundSoybean (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.ResultsWe 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.ConclusionsSimultaneous 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.

Highlights

  • Soybean (Glycine max) is a major protein crop, because soybean protein has an amino acid score comparable to that of beef and egg white

  • To produce hypoallergenic soybeans without impairing the processing properties, we focused on two allergenic proteins, Gly m Bd 28 K and Gly m Bd 30 K, because no pyramiding of mutant alleles of these allergens in soybean has been reported

  • Our results demonstrate the applicability of the clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated endonuclease 9 (Cas9) system for the production of hypoallergenic soybean plants

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Summary

Introduction

Soybean (Glycine max) is a major protein crop, because soybean protein has an amino acid score comparable to that of beef and egg white. A decrease in allergenic protein levels would be useful for expanding the market for soybean proteins and processed foods. The CRISPR/Cas 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. Soybean (Glycine max, 2n = 2x = 40) is one of the most important protein crops used for food and forage worldwide, because its seeds contain high-quality proteins with an amino acid score comparable to that of beef and egg white [1]. Development of hypoallergenic soybean varieties or establishment of a procedure to remove allergens would be useful for expanding the market of soybean proteins and processed foods

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