Details
Original language | English |
---|---|
Pages (from-to) | 649-663 |
Number of pages | 15 |
Journal | Plant Journal |
Volume | 109 |
Issue number | 3 |
Early online date | 16 Nov 2021 |
Publication status | Published - 29 Jan 2022 |
Abstract
Food allergies are a major health issue worldwide. Modern breeding techniques such as genome editing via CRISPR/Cas9 have the potential to mitigate this by targeting allergens in plants. This study addressed the major allergen Bra j I, a seed storage protein of the 2S albumin class, in the allotetraploid brown mustard (Brassica juncea). Cotyledon explants of an Indian gene bank accession (CR2664) and the German variety Terratop were transformed using Agrobacterium tumefaciens harboring binary vectors with multiple single guide RNAs to induce either large deletions or frameshift mutations in both Bra j I homoeologs. A total of 49 T 0 lines were obtained with up to 3.8% transformation efficiency. Four lines had large deletions of 566 up to 790 bp in the Bra j IB allele. Among 18 Terratop T 0 lines, nine carried indels in the targeted regions. From 16 analyzed CR2664 T 0 lines, 14 held indels and three had all four Bra j I alleles mutated. The majority of the CRISPR/Cas9-induced mutations were heritable to T 1 progenies. In some edited lines, seed formation and viability were reduced and seeds showed a precocious development of the embryo leading to a rupture of the testa already in the siliques. Immunoblotting using newly developed Bra j I-specific antibodies revealed the amount of Bra j I protein to be reduced or absent in seed extracts of selected lines. Removing an allergenic determinant from mustard is an important first step towards the development of safer food crops.
Keywords
- Bra j I, CRISPR/Cas, food allergen, mustard, seed storage protein, transformation
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)
- Genetics
- Agricultural and Biological Sciences(all)
- Plant Science
- Biochemistry, Genetics and Molecular Biology(all)
- Cell Biology
Cite this
- Standard
- Harvard
- Apa
- Vancouver
- BibTeX
- RIS
In: Plant Journal, Vol. 109, No. 3, 29.01.2022, p. 649-663.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Removing the major allergen Bra j I from brown mustard (Brassica juncea) by CRISPR/Cas9
AU - Assou, Juvenal
AU - Zhang, Dingbo
AU - Roth, Kristian D R
AU - Steinke, Stephan
AU - Hust, Michael
AU - Reinard, Thomas
AU - Winkelmann, Traud
AU - Boch, Jens
N1 - Funding information: This work was supported by funding from the Federal Ministry of Education and Research (BMBF LACOP consortium; grant number 031B0348). The authors thank Ewa Schneider for excellent technical assistance, David Wamhoff for help in statistics, and Jana Streubel for MoClo?compatible genome editing vectors. Open access funding enabled and organized by ProjektDEAL.
PY - 2022/1/29
Y1 - 2022/1/29
N2 - Food allergies are a major health issue worldwide. Modern breeding techniques such as genome editing via CRISPR/Cas9 have the potential to mitigate this by targeting allergens in plants. This study addressed the major allergen Bra j I, a seed storage protein of the 2S albumin class, in the allotetraploid brown mustard (Brassica juncea). Cotyledon explants of an Indian gene bank accession (CR2664) and the German variety Terratop were transformed using Agrobacterium tumefaciens harboring binary vectors with multiple single guide RNAs to induce either large deletions or frameshift mutations in both Bra j I homoeologs. A total of 49 T 0 lines were obtained with up to 3.8% transformation efficiency. Four lines had large deletions of 566 up to 790 bp in the Bra j IB allele. Among 18 Terratop T 0 lines, nine carried indels in the targeted regions. From 16 analyzed CR2664 T 0 lines, 14 held indels and three had all four Bra j I alleles mutated. The majority of the CRISPR/Cas9-induced mutations were heritable to T 1 progenies. In some edited lines, seed formation and viability were reduced and seeds showed a precocious development of the embryo leading to a rupture of the testa already in the siliques. Immunoblotting using newly developed Bra j I-specific antibodies revealed the amount of Bra j I protein to be reduced or absent in seed extracts of selected lines. Removing an allergenic determinant from mustard is an important first step towards the development of safer food crops.
AB - Food allergies are a major health issue worldwide. Modern breeding techniques such as genome editing via CRISPR/Cas9 have the potential to mitigate this by targeting allergens in plants. This study addressed the major allergen Bra j I, a seed storage protein of the 2S albumin class, in the allotetraploid brown mustard (Brassica juncea). Cotyledon explants of an Indian gene bank accession (CR2664) and the German variety Terratop were transformed using Agrobacterium tumefaciens harboring binary vectors with multiple single guide RNAs to induce either large deletions or frameshift mutations in both Bra j I homoeologs. A total of 49 T 0 lines were obtained with up to 3.8% transformation efficiency. Four lines had large deletions of 566 up to 790 bp in the Bra j IB allele. Among 18 Terratop T 0 lines, nine carried indels in the targeted regions. From 16 analyzed CR2664 T 0 lines, 14 held indels and three had all four Bra j I alleles mutated. The majority of the CRISPR/Cas9-induced mutations were heritable to T 1 progenies. In some edited lines, seed formation and viability were reduced and seeds showed a precocious development of the embryo leading to a rupture of the testa already in the siliques. Immunoblotting using newly developed Bra j I-specific antibodies revealed the amount of Bra j I protein to be reduced or absent in seed extracts of selected lines. Removing an allergenic determinant from mustard is an important first step towards the development of safer food crops.
KW - Bra j I
KW - CRISPR/Cas
KW - food allergen
KW - mustard
KW - seed storage protein
KW - transformation
UR - http://www.scopus.com/inward/record.url?scp=85120429845&partnerID=8YFLogxK
U2 - 10.1111/tpj.15584
DO - 10.1111/tpj.15584
M3 - Article
C2 - 34784073
VL - 109
SP - 649
EP - 663
JO - Plant Journal
JF - Plant Journal
SN - 0960-7412
IS - 3
ER -