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LbCas12a介导的对……的抑制

LbCas12a mediated suppression of .

作者信息

Ashraf Sidra, Ahmad Aftab, Khan Sultan Habibullah, Jamil Amer, Sadia Bushra, Brown Judith K

机构信息

Department of Biochemistry, University of Agriculture, Faisalabad, Pakistan.

Cotton Biotechnology Lab, Center for Advanced Studies in Agriculture and Food Security (CASAFS), University of Agriculture, Faisalabad, Pakistan.

出版信息

Front Plant Sci. 2023 Aug 11;14:1233295. doi: 10.3389/fpls.2023.1233295. eCollection 2023.

Abstract

Begomoviruses are contagious and severely affect commercially important fiber and food crops. (CLCuMuV) is one of the most dominant specie of and a major constraint on cotton yield in Pakistan. Currently, the field of plant genome editing is being revolutionized by the CRISPR/Cas system applications such as base editing, prime editing and CRISPR based gene drives. CRISPR/Cas9 system has successfully been used against biotic and abiotic plant stresses with proof-of-concept studies in both model and crop plants. CRISPR/Cas12 and CRISPR/Cas13 have recently been applied in plant sciences for basic and applied research. In this study, we used a novel approach, multiplexed crRNA-based Cas12a toolbox to target the different ORFs of the CLCuMuV genome at multiple sites simultaneously. This method successfully eliminated the symptoms of CLCuMuV in and . Three individual crRNAs were designed from the CLCuMuV genome, targeting the specific sites of four different ORFs (C1, V1 and overlapping region of C2 and C3). The Cas12a-based construct Cas12a-MV was designed through Golden Gate three-way cloning for precise editing of CLCuMuV genome. Cas12a-MV construct was confirmed through whole genome sequencing using the primers Ubi-intron-F1 and M13-R1. Transient assays were performed in 4 weeks old plants, through the agroinfiltration method. Sanger sequencing indicated that the Cas12a-MV constructs made a considerable mutations at the target sites of the viral genome. In addition, TIDE analysis of Sanger sequencing results showed the editing efficiency of crRNA1 (21.7%), crRNA2 (24.9%) and crRNA3 (55.6%). Furthermore, the Cas12a-MV construct was stably transformed into through the leaf disc method to evaluate the potential of transgenic plants against CLCuMuV. For transgene analysis, the DNA of transgenic plants of was subjected to PCR to amplify Cas12a genes with specific primers. Infectious clones were agro-inoculated in transgenic and non-transgenic plants (control) for the infectivity assay. The transgenic plants containing Cas12a-MV showed rare symptoms and remained healthy compared to control plants with severe symptoms. The transgenic plants containing Cas12a-MV showed a significant reduction in virus accumulation (0.05) as compared to control plants (1.0). The results demonstrated the potential use of the multiplex LbCas12a system to develop virus resistance in model and crop plants against begomoviruses.

摘要

双生病毒具有传染性,会严重影响具有重要商业价值的纤维作物和粮食作物。(棉花曲叶多胚病毒)是双生病毒中最主要的种类之一,也是巴基斯坦棉花产量的主要限制因素。目前,植物基因组编辑领域正因CRISPR/Cas系统的应用而发生变革,如碱基编辑、引导编辑和基于CRISPR的基因驱动。CRISPR/Cas9系统已成功用于应对植物的生物和非生物胁迫,并在模式植物和作物中进行了概念验证研究。CRISPR/Cas12和CRISPR/Cas13最近已应用于植物科学的基础研究和应用研究。在本研究中,我们采用了一种新方法,即基于多重crRNA的Cas12a工具箱,同时在多个位点靶向棉花曲叶多胚病毒基因组的不同开放阅读框。该方法成功消除了棉花曲叶多胚病毒在[具体植物1]和[具体植物2]中的症状。从棉花曲叶多胚病毒基因组设计了三个单独的crRNA,靶向四个不同开放阅读框(C1、V1以及C2和C3的重叠区域)的特定位点。通过金门三向克隆设计了基于Cas12a的构建体Cas12a-MV,用于精确编辑棉花曲叶多胚病毒基因组。使用引物Ubi-intron-F1和M13-R1通过全基因组测序确认了Cas12a-MV构建体。通过农杆菌浸润法在4周龄的[具体植物3]植株中进行瞬时分析。桑格测序表明,Cas12a-MV构建体在病毒基因组的靶位点产生了大量突变。此外,对桑格测序结果的TIDE分析显示,crRNA1的编辑效率为21.7%,crRNA2为24.9%,crRNA3为55.6%。此外,通过叶盘法将Cas12a-MV构建体稳定转化到[具体植物4]中,以评估转基因植物对棉花曲叶多胚病毒的抗性潜力。为了进行转基因分析,对[具体植物4]转基因植株的DNA进行PCR,用特异性引物扩增Cas12a基因。将感染性克隆通过农杆菌接种到转基因植物和非转基因植物(对照)中进行感染性测定。与出现严重症状的对照植物相比,含有Cas12a-MV的转基因植物症状罕见且保持健康。与对照植物(病毒积累量为1.0)相比,含有Cas12a-MV的转基因植物的病毒积累量显著降低(0.05)。结果证明了多重LbCas12a系统在模式植物和作物中针对双生病毒培育抗病毒性方面的潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e866/10456881/13385a3ab45a/fpls-14-1233295-g001.jpg

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