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Engineering DNA nanostructures for siRNA delivery in plants

Zhang, Huan and Zhang, Honglu and Demirer, Gozde S. and González-Grandío, Eduardo and Fan, Chunhai and Landry, Markita P. (2020) Engineering DNA nanostructures for siRNA delivery in plants. Nature Protocols, 15 (9). pp. 3064-3087. ISSN 1754-2189. doi:10.1038/s41596-020-0370-0. https://resolver.caltech.edu/CaltechAUTHORS:20220302-323737000

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Image (JPEG) (Supplementary Figure 1: Representative gel image for characterization of the formation of DNA nanostructures) - Supplemental Material
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Image (JPEG) (Supplementary Figure 2: Infiltration of leaves with 1-ml syringe) - Supplemental Material
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Image (JPEG) (Supplementary Figure 3: Confirmation of strong GFP expression in transgenic mGFP5 Nb plants) - Supplemental Material
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Image (JPEG) (Supplementary Figure 4: Internalization of Cy3-labeled DHT monomer into three different plant species) - Supplemental Material
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Image (JPEG) (Supplementary Figure 5 Representative confocal images to test the internalization mechanism of the Cy3-labeled DHT monomer into Nb leaves) - Supplemental Material
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Image (JPEG) (Supplementary Figure 6: DNA nanostructure-induced GFP silencing is transient) - Supplemental Material
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Image (JPEG) (Supplementary Figure 7: Gene silencing pathways for siRNA-linked nanostructures) - Supplemental Material
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Image (JPEG) (Supplementary Figure 8: DNA nanostructures without siRNA loading cause no change in GFP mRNA) - Supplemental Material
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Image (JPEG) (Supplementary Figure 9: DNA nanostructure-infiltrated Nb leaves show no stress response as measured by qPCR) - Supplemental Material
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Image (JPEG) (Supplementary Figure 10: Silencing of endogenous functional Nb ROQ1 gene with siRNA loaded on tetrahedron DNA nanostructures) - Supplemental Material
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Image (JPEG) (Supplementary Figure 11: DNA nanostructures are gradually degraded in plant cell lysate) - Supplemental Material
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[img] PDF (Supplementary Figures 1–11, Tables 1 and 2 and Discussion) - Supplemental Material
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Abstract

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.


Item Type:Article
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https://doi.org/10.1038/s41596-020-0370-0DOIArticle
https://rdcu.be/cH6MVPublisherFree ReadCube access
ORCID:
AuthorORCID
Zhang, Huan0000-0002-1096-4255
Demirer, Gozde S.0000-0002-3007-1489
González-Grandío, Eduardo0000-0002-2059-4542
Landry, Markita P.0000-0002-5832-8522
Additional Information:© 2020 Nature Publishing Group. Received 14 December 2019. Accepted 29 May 2020. Published 17 August 2020. Issue Date September 2020. Hu. Z. acknowledges the support of the Chinese National Natural Science Foundation (21605153). The authors acknowledge support from a Burroughs Wellcome Fund Career Award at the Scientific Interface (CASI), a Stanley Fahn PDF Junior Faculty Grant under award no. PF-JFA-1760, a Beckman Foundation Young Investigator Award, a USDA AFRI award, a grant from the Gordon and Betty Moore Foundation, a USDA NIFA award, a USDA-BBT EAGER award, support from the Chan-Zuckerberg Foundation and an FFAR New Innovator Award (to M.P.L.). G.S.D. is supported by a Schlumberger Foundation Faculty for the Future Fellowship. The authors also acknowledge support from UC Berkeley Molecular Imaging Center (supported by the Gordon and Betty Moore Foundation), the QB3 Shared Stem Cell Facility and the Innovative Genomics Institute (IGI). Reporting Summary. Further information on research design is available in the Nature Research Reporting Summary linked to this article. Data availability. All materials are available from commercial sources or can be derived using methods described in this study. All data and controls relevant to the protocol have been included in the Supplementary Information. Raw data such as unprocessed image files can be obtained from the corresponding author upon reasonable request. Contributions. Hu. Z. and M.P.L designed the experiments, and C.F. helped with the experimental design. Hu. Z. and Ho. Z. performed the simulations and experiments. Hu. Z. and G.S.D analyzed the data and created the figures. Hu. Z., Ho. Z., G.S.D, and E.G.-G. wrote the manuscript. All authors revised and approved the manuscript. The authors declare no competing interests. Peer review information. Nature Protocols thanks Veikko Linko and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
Funders:
Funding AgencyGrant Number
National Natural Science Foundation of China21605153
Burroughs Wellcome FundUNSPECIFIED
Parkinson's FoundationPF-JFA-1760
Arnold and Mabel Beckman FoundationUNSPECIFIED
Department of AgricultureUNSPECIFIED
Gordon and Betty Moore FoundationUNSPECIFIED
Chan-Zuckerberg FoundationUNSPECIFIED
Foundation for Food ResearchUNSPECIFIED
Schlumberger FoundationUNSPECIFIED
Innovative Genomics InstituteUNSPECIFIED
Issue or Number:9
DOI:10.1038/s41596-020-0370-0
Record Number:CaltechAUTHORS:20220302-323737000
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20220302-323737000
Official Citation:Zhang, H., Zhang, H., Demirer, G.S. et al. Engineering DNA nanostructures for siRNA delivery in plants. Nat Protoc 15, 3064–3087 (2020). https://doi.org/10.1038/s41596-020-0370-0
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:113692
Collection:CaltechAUTHORS
Deposited By: George Porter
Deposited On:03 Mar 2022 19:20
Last Modified:03 Mar 2022 19:20

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