4.7 Article

Carbon Nanotube-Mediated Plasmid DNA Delivery in Rice Leaves and Seeds

Journal

Publisher

MDPI
DOI: 10.3390/ijms23084081

Keywords

gene editing; rice (Oryza sativa); CRISPR; Cas9; carbon nanotubes (CNTs); phytoene desaturase (PDS)

Funding

  1. Texas A&M AgriLife Research
  2. Texas A&M University X-Grant project through the President's Excellence Fund
  3. Agriculture and Food Research Initiative [2020-67013-31811]
  4. USDA National Institute of Food and Agriculture

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CRISPR-Cas gene editing technologies have the potential to precisely modify crops. However, in vitro plant transformation and regeneration techniques pose challenges. This study investigates transformation methods that can directly alter germline cells, eliminating the need for in vitro plant regeneration. The results suggest that CNT-based delivery of plasmid DNA appears promising for in planta transformation, enabling high-throughput gene editing to accelerate functional genomics and crop improvement activities.
CRISPR-Cas gene editing technologies offer the potential to modify crops precisely; however, in vitro plant transformation and regeneration techniques present a bottleneck due to the lengthy and genotype-specific tissue culture process. Ideally, in planta transformation can bypass tissue culture and directly lead to transformed plants, but efficient in planta delivery and transformation remains a challenge. This study investigates transformation methods that have the potential to directly alter germline cells, eliminating the challenge of in vitro plant regeneration. Recent studies have demonstrated that carbon nanotubes (CNTs) loaded with plasmid DNA can diffuse through plant cell walls, facilitating transient expression of foreign genetic elements in plant tissues. To test if this approach is a viable technique for in planta transformation, CNT-mediated plasmid DNA delivery into rice tissues was performed using leaf and excised-embryo infiltration with reporter genes. Quantitative and qualitative data indicate that CNTs facilitate plasmid DNA delivery in rice leaf and embryo tissues, resulting in transient GFP, YFP, and GUS expression. Experiments were also initiated with CRISPR-Cas vectors targeting the phytoene desaturase (PDS) gene for CNT delivery into mature embryos to create heritable genetic edits. Overall, the results suggest that CNT-based delivery of plasmid DNA appears promising for in planta transformation, and further optimization can enable high-throughput gene editing to accelerate functional genomics and crop improvement activities.

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