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CRISPR/Cas9介导的γ-和ω-醇溶蛋白多重基因编辑:为无醇溶蛋白小麦铺平道路。

CRISPR/Cas9-mediated multiplex gene editing of gamma and omega gliadins: paving the way for gliadin-free wheat.

作者信息

Sánchez-León Susana, Marín-Sanz Miriam, Guzmán-López María H, Gavilán-Camacho Marta, Simón Edurne, Barro Francisco

机构信息

Department of Plant Breeding, Institute for Sustainable Agriculture (IAS-CSIC), E-14004 Córdoba, Spain.

GLUTEN 3S Research Group, Department of Nutrition and Food Science, University of the Basque Country, Vitoria-Gasteiz, 01006, Spain.

出版信息

J Exp Bot. 2024 Dec 4;75(22):7079-7095. doi: 10.1093/jxb/erae376.

DOI:10.1093/jxb/erae376
PMID:39238167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11630021/
Abstract

Wheat is a staple cereal in the human diet. Despite its significance, an increasing percentage of the population suffers adverse reactions to wheat, which are triggered by wheat gluten, particularly the gliadin fractions. In this study, we employed CRISPR/Cas [clustered regularly interspaced palindromic repeats (CRISPR)/CRISPR-associated protein] multiplexing to introduce targeted mutations into γ- and ω-gliadin genes of wheat, to produce lines deficient in one or both immunogenic gliadin fractions simultaneously. For this study, eight single guide RNAs (sgRNAs) were designed and combined into four plasmids to produce 59 modified wheat lines, of which 20 exhibited mutations in the target genes. Characterization of these lines through Sanger sequencing or next-generation sequencing revealed a complex pattern of InDels, including deletions spanning multiple sgRNAs. The mutations were transmitted to the offspring, and the analysis of homozygous derived lines by reverse-phase HPLC and monoclonal antibodies showed a 97.7% reduction in gluten content. Crossing these lines with other CRISPR/Cas lines deficient in the α-gliadins allowed multiple mutations to be combined. This work represents an important step forward in the use of CRISPR/Cas to develop gluten-free wheat.

摘要

小麦是人类饮食中的主要谷物。尽管其具有重要意义,但越来越多的人对小麦产生不良反应,这些反应由小麦面筋引发,尤其是麦醇溶蛋白组分。在本研究中,我们采用CRISPR/Cas(成簇规律间隔短回文重复序列/CRISPR相关蛋白)多路复用技术,将靶向突变引入小麦的γ-和ω-麦醇溶蛋白基因,以同时产生缺乏一种或两种免疫原性麦醇溶蛋白组分的品系。在本研究中,设计了8个单向导RNA(sgRNA)并组合到4个质粒中,以产生59个改良小麦品系,其中20个在靶基因中表现出突变。通过桑格测序或下一代测序对这些品系进行表征,揭示了一个复杂的插入缺失模式,包括跨越多个sgRNA的缺失。这些突变传递给了后代,通过反相高效液相色谱和单克隆抗体对纯合衍生品系的分析表明,面筋含量降低了97.7%。将这些品系与其他缺乏α-麦醇溶蛋白的CRISPR/Cas品系杂交,可以组合多个突变。这项工作代表了利用CRISPR/Cas开发无麸质小麦方面向前迈出的重要一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/b4edebc24cba/erae376_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/d35c058a86c7/erae376_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/197cf6988767/erae376_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/286f61116944/erae376_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/61293c7e1123/erae376_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/89e2614c0510/erae376_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/b4edebc24cba/erae376_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/d35c058a86c7/erae376_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/197cf6988767/erae376_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/286f61116944/erae376_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/61293c7e1123/erae376_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/89e2614c0510/erae376_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f22/11630021/b4edebc24cba/erae376_fig6.jpg

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本文引用的文献

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