4.7 Article

Engineering DNA nanostructures for siRNA delivery in plants

Journal

NATURE PROTOCOLS
Volume 15, Issue 9, Pages 3064-3087

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41596-020-0370-0

Keywords

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Funding

  1. Chinese National Natural Science Foundation [21605153]
  2. Burroughs Wellcome Fund Career Award at the Scientific Interface (CASI)
  3. Stanley Fahn PDF Junior Faculty Grant [PF-JFA-1760]
  4. Beckman Foundation Young Investigator Award
  5. USDA AFRI award
  6. Gordon and Betty Moore Foundation
  7. USDA NIFA award
  8. USDA-BBT EAGER award
  9. Chan-Zuckerberg Foundation
  10. FFAR New Innovator Award
  11. Schlumberger Foundation
  12. UC Berkeley Molecular Imaging Center (Gordon and Betty Moore Foundation)
  13. QB3 Shared Stem Cell Facility
  14. Innovative Genomics Institute (IGI)

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This protocol describes how to engineer DNA nanostructures with different sizes, shapes and mechanical properties; load them with a siRNA cargo; and evaluate their ability to silence genes in mature tobacco plants. Targeted downregulation of select endogenous plant genes is known to confer disease or pest resistance in crops and is routinely accomplished via transgenic modification of plants for constitutive gene silencing. An attractive alternative to the use of transgenics or pesticides in agriculture is the use of a 'green' alternative known as RNAi, which involves the delivery of siRNAs that downregulate endogenous genes to confer resistance. However, siRNA is a molecule that is highly susceptible to enzymatic degradation and is difficult to deliver across the lignin-rich and multi-layered plant cell wall that poses the dominant physical barrier to biomolecule delivery in plants. We have demonstrated that DNA nanostructures can be utilized as a cargo carrier for direct siRNA delivery and gene silencing in mature plants. The size, shape, compactness and stiffness of the DNA nanostructure affect both internalization into plant cells and subsequent gene silencing efficiency. Herein, we provide a detailed protocol that can be readily adopted with standard biology benchtop equipment to generate geometrically optimized DNA nanostructures for transgene-free and force-independent siRNA delivery and gene silencing in mature plants. We further discuss how such DNA nanostructures can be rationally designed to efficiently enter plant cells and deliver cargoes to mature plants, and provide guidance for DNA nanostructure characterization, storage and use. The protocol described herein can be completed in 4 d.

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