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LbCas12a mediated suppression of . | LitMetric

LbCas12a mediated suppression of .

Front Plant Sci

School of Plant Sciences, University of Arizona, Tucson, AZ, United States.

Published: August 2023

AI Article Synopsis

  • Begomoviruses, particularly CLCuMuV, are a significant threat to cotton crops in Pakistan, leading to decreased yields.
  • The study explores the use of a novel CRISPR/Cas12a system to target and edit the viral genome of CLCuMuV, demonstrating successful elimination of virus symptoms in tested plants.
  • The editing efficiency of different crRNAs was assessed, leading to stable transformation of the Cas12a construct into plants to test its effectiveness against CLCuMuV.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456881PMC
http://dx.doi.org/10.3389/fpls.2023.1233295DOI Listing

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