The α-Gliadins in Bread Wheat: Effect of Nitrogen Treatment on the Expression of the Major Celiac Disease Immunogenic Complex in Two RNAi Low-Gliadin Lines
Celiac Disease (CD) is an autoimmune disorder that affects approximately 1% of the worldwide population. The α-gliadins of wheat contain the 33-mer peptide, the most active peptide in CD both in adults and pediatric patients. In this study, we have characterized the variants and expression profile of an α-gliadins amplicon, harboring the 33-mer peptide, in two low-gliadin RNAi wheat lines, under two different Nitrogen (N) treatments. We estimated that the amplicon expands 45 different α-gliadin variants with high variability due to length, randomly distributed SNPs, and the presence of encoded CD epitopes. Expression of this amplicon is reduced in both RNAi lines in comparison to the wild type. High N treatment significantly increases transcripts of the amplicon in the wild type, but not in the transgenic lines. Classification of α-gliadin variants, considering the number of epitopes, revealed that amplicon variants containing the full complement of 33-mer peptide were affected by N treatment, increasing their expression when N was increased. Line D793 provided higher and more stable silencing through different N fertilization regimes, expressing fewer CD epitopes than D783. Results of this study are important for better understanding of RNAi α-gliadin silencing in response to N treatments, and for undertaking new strategies by RNAi or CRISPR/Cas toward obtaining new varieties suitable for people suffering gluten intolerances.
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Frontiers Media
2021-04-29
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Subjects: | α-gliadins, Nitrogen, RNAi wheat, Celiac disease, Endosperm-specific promoters, Gluten, 33-mer, |
Online Access: | http://hdl.handle.net/10261/268128 http://dx.doi.org/10.13039/501100000780 http://dx.doi.org/10.13039/501100004837 |
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dig-ias-es-10261-2681282022-04-29T02:19:28Z The α-Gliadins in Bread Wheat: Effect of Nitrogen Treatment on the Expression of the Major Celiac Disease Immunogenic Complex in Two RNAi Low-Gliadin Lines Sánchez-León, Susana Giménez, María J. Barro Losada, Francisco Ministerio de Ciencia e Innovación (España) European Commission α-gliadins Nitrogen RNAi wheat Celiac disease Endosperm-specific promoters Gluten 33-mer Celiac Disease (CD) is an autoimmune disorder that affects approximately 1% of the worldwide population. The α-gliadins of wheat contain the 33-mer peptide, the most active peptide in CD both in adults and pediatric patients. In this study, we have characterized the variants and expression profile of an α-gliadins amplicon, harboring the 33-mer peptide, in two low-gliadin RNAi wheat lines, under two different Nitrogen (N) treatments. We estimated that the amplicon expands 45 different α-gliadin variants with high variability due to length, randomly distributed SNPs, and the presence of encoded CD epitopes. Expression of this amplicon is reduced in both RNAi lines in comparison to the wild type. High N treatment significantly increases transcripts of the amplicon in the wild type, but not in the transgenic lines. Classification of α-gliadin variants, considering the number of epitopes, revealed that amplicon variants containing the full complement of 33-mer peptide were affected by N treatment, increasing their expression when N was increased. Line D793 provided higher and more stable silencing through different N fertilization regimes, expressing fewer CD epitopes than D783. Results of this study are important for better understanding of RNAi α-gliadin silencing in response to N treatments, and for undertaking new strategies by RNAi or CRISPR/Cas toward obtaining new varieties suitable for people suffering gluten intolerances. The Spanish Ministry of Science and Innovation (Project PID2019-110847RB-I00) and the European Regional Development Fund (FEDER) supported this work. 2022-04-28T10:00:11Z 2022-04-28T10:00:11Z 2021-04-29 2022-04-28T10:00:11Z artículo http://purl.org/coar/resource_type/c_6501 doi: 10.3389/fpls.2021.663653 e-issn: 1664-462X Frontiers in Plant Science 12: 663653 (2021) http://hdl.handle.net/10261/268128 10.3389/fpls.2021.663653 http://dx.doi.org/10.13039/501100000780 http://dx.doi.org/10.13039/501100004837 #PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-110847RB-I00/ES/REDISEÑO DE LAS PROTEINAS INMUNOGENICAS DE TRIGO RELACIONADAS CON LA CELIAQUIA MEDIANTE CRISPR%2FCAS/ Publisher's version http://dx.doi.org/10.3389/fpls.2021.663653 Sí open Frontiers Media |
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α-gliadins Nitrogen RNAi wheat Celiac disease Endosperm-specific promoters Gluten 33-mer α-gliadins Nitrogen RNAi wheat Celiac disease Endosperm-specific promoters Gluten 33-mer |
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α-gliadins Nitrogen RNAi wheat Celiac disease Endosperm-specific promoters Gluten 33-mer α-gliadins Nitrogen RNAi wheat Celiac disease Endosperm-specific promoters Gluten 33-mer Sánchez-León, Susana Giménez, María J. Barro Losada, Francisco The α-Gliadins in Bread Wheat: Effect of Nitrogen Treatment on the Expression of the Major Celiac Disease Immunogenic Complex in Two RNAi Low-Gliadin Lines |
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Celiac Disease (CD) is an autoimmune disorder that affects approximately 1% of the worldwide population. The α-gliadins of wheat contain the 33-mer peptide, the most active peptide in CD both in adults and pediatric patients. In this study, we have characterized the variants and expression profile of an α-gliadins amplicon, harboring the 33-mer peptide, in two low-gliadin RNAi wheat lines, under two different Nitrogen (N) treatments. We estimated that the amplicon expands 45 different α-gliadin variants with high variability due to length, randomly distributed SNPs, and the presence of encoded CD epitopes. Expression of this amplicon is reduced in both RNAi lines in comparison to the wild type. High N treatment significantly increases transcripts of the amplicon in the wild type, but not in the transgenic lines. Classification of α-gliadin variants, considering the number of epitopes, revealed that amplicon variants containing the full complement of 33-mer peptide were affected by N treatment, increasing their expression when N was increased. Line D793 provided higher and more stable silencing through different N fertilization regimes, expressing fewer CD epitopes than D783. Results of this study are important for better understanding of RNAi α-gliadin silencing in response to N treatments, and for undertaking new strategies by RNAi or CRISPR/Cas toward obtaining new varieties suitable for people suffering gluten intolerances. |
author2 |
Ministerio de Ciencia e Innovación (España) |
author_facet |
Ministerio de Ciencia e Innovación (España) Sánchez-León, Susana Giménez, María J. Barro Losada, Francisco |
format |
artículo |
topic_facet |
α-gliadins Nitrogen RNAi wheat Celiac disease Endosperm-specific promoters Gluten 33-mer |
author |
Sánchez-León, Susana Giménez, María J. Barro Losada, Francisco |
author_sort |
Sánchez-León, Susana |
title |
The α-Gliadins in Bread Wheat: Effect of Nitrogen Treatment on the Expression of the Major Celiac Disease Immunogenic Complex in Two RNAi Low-Gliadin Lines |
title_short |
The α-Gliadins in Bread Wheat: Effect of Nitrogen Treatment on the Expression of the Major Celiac Disease Immunogenic Complex in Two RNAi Low-Gliadin Lines |
title_full |
The α-Gliadins in Bread Wheat: Effect of Nitrogen Treatment on the Expression of the Major Celiac Disease Immunogenic Complex in Two RNAi Low-Gliadin Lines |
title_fullStr |
The α-Gliadins in Bread Wheat: Effect of Nitrogen Treatment on the Expression of the Major Celiac Disease Immunogenic Complex in Two RNAi Low-Gliadin Lines |
title_full_unstemmed |
The α-Gliadins in Bread Wheat: Effect of Nitrogen Treatment on the Expression of the Major Celiac Disease Immunogenic Complex in Two RNAi Low-Gliadin Lines |
title_sort |
α-gliadins in bread wheat: effect of nitrogen treatment on the expression of the major celiac disease immunogenic complex in two rnai low-gliadin lines |
publisher |
Frontiers Media |
publishDate |
2021-04-29 |
url |
http://hdl.handle.net/10261/268128 http://dx.doi.org/10.13039/501100000780 http://dx.doi.org/10.13039/501100004837 |
work_keys_str_mv |
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