Related Experiment Video
Updated: Sep 21, 2025

10:14
Double-stranded RNA Oral Delivery Methods to Induce RNA Interference in Phloem and Plant-sap-feeding Hemipteran Insects
Published on: May 4, 2018
14.0K
Carbon Dots Boost dsRNA Delivery in Plants and Increase Local and Systemic siRNA Production
Josemaría Delgado-Martín1,2, Alejo Delgado-Olidén1, Leonardo Velasco1
1Instituto Andaluz de Investigación y Formación Agraria (IFAPA), Churriana, 290140 Malaga, Spain.
International Journal of Molecular Sciences
|May 28, 2022
Summary
Carbon dots (CDs) enhance the foliar delivery of double-stranded RNA (dsRNA) in plants. This dsRNA nanocomposite formulation significantly increases dsRNA uptake and systemic movement for RNA interference applications.
Area of Science:
- Plant Science
- Nanotechnology
- Biochemistry
Background:
- RNA interference (RNAi) holds promise for crop protection.
- Efficient delivery of double-stranded RNA (dsRNA) into plants remains a challenge for foliar applications.
Purpose of the Study:
- To develop and evaluate carbon dots (CDs) as a carrier for dsRNA foliar delivery in plants.
- To assess the efficacy of CD-dsRNA nanocomposites in enhancing dsRNA uptake and systemic movement.
Main Methods:
- Carbon dots synthesized from glucose/saccharose and passivated with polyethylenimines.
- Characterization of CDs using hydrodynamic analysis, TEM, XPS, and FTIR.
- Delivery of naked or CD-coated dsRNA to cucumber leaves via spraying and subsequent quantification of dsRNA and siRNAs.
Main Results:
- CDs possess positive charges, suitable for dsRNA nanocomposite formation.
- CD-dsRNA nanocomposites increased dsRNA leaf entry by 50-fold compared to naked dsRNA.
- Systemic dsRNA and siRNA accumulation in distal leaves significantly increased with CD-dsRNA nanocomposite delivery.
- FITC-labeled dsRNA showed enhanced apoplastic accumulation and plant entry when coated with CDs.
Conclusions:
- Hydrothermally synthesized carbon dots are effective carriers for dsRNA foliar delivery.
- CD-dsRNA nanocomposites enhance dsRNA uptake, translocation, and RNAi efficacy in plants.
- This approach offers a promising strategy for developing sustainable agricultural pest and disease management solutions.
More Related Videos
Related Concept Videos
Experimental RNAi
6.3K
RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
6.3K
siRNA - Small Interfering RNAs
17.0K
Small interfering RNAs, or siRNAs, are short regulatory RNA molecules that can silence genes post-transcriptionally, as well as the transcriptional level in some cases. siRNAs are important for protecting cells against viral infections and silencing transposable genetic elements.
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...
17.0K
RNA Interference
26.5K
RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
26.5K

