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Related Concept Videos

RNA Interference01:23

RNA Interference

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...
Experimental RNAi02:15

Experimental RNAi

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...
Types of RNA01:23

Types of RNA

Overview
Three main types of RNA are involved in protein synthesis: messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). These RNAs perform diverse functions and can be broadly classified as protein-coding or non-coding RNA. Non-coding RNAs play important roles in the regulation of gene expression in response to developmental and environmental changes. Non-coding RNAs in prokaryotes can be manipulated to develop more effective antibacterial drugs for human or animal use.
RNA...
lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA (lncRNA)...
Microbial Interactions: Cooperation01:26

Microbial Interactions: Cooperation

Microbial cooperation involves beneficial interactions in which different species work together for individual or mutual advantage. These interactions can profoundly influence ecological dynamics and evolutionary processes, and they are essential to many pathogenic and symbiotic relationships.Nematode–Bacteria CooperationA striking example is the relationship between the Gram-negative bacterium Xenorhabdus nematophila and the parasitic nematode Steinernema carpocapsae. Juvenile nematodes...

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Related Experiment Video

Updated: Jun 16, 2026

Application of RNA Interference in the Pinewood Nematode, Bursaphelenchus xylophilus
06:54

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Published on: March 9, 2022

Lactobacillus-mediated RNA interference in nematode.

Ai Kuwahara1, Masashi Arita, Akira Kushiro

  • 1Department of Bioscience and Biotechnology, Okayama University, 3-1-1 Tsushimanaka, Okayama, Japan.

Journal of Bioscience and Bioengineering
|February 5, 2010
PubMed
Summary

Engineered bacteria Lactobacillus paracasei produce dsRNA for RNA interference, silencing essential genes in Caenorhabditis elegans. This engineered microbe serves as a potential oral dsRNA delivery system for research and therapeutic applications.

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Area of Science:

  • Microbiology
  • Genetics
  • Molecular Biology

Background:

  • RNA interference (RNAi) is a powerful gene-silencing mechanism.
  • Developing efficient and safe delivery systems for RNAi therapeutics is crucial.
  • Caenorhabditis elegans is a widely used model organism for genetic studies.

Purpose of the Study:

  • To engineer Lactobacillus paracasei to produce double-stranded RNA (dsRNA).
  • To demonstrate the efficacy of dsRNA produced by L. paracasei in silencing an essential gene in Caenorhabditis elegans.
  • To evaluate the potential of L. paracasei as an oral dsRNA delivery vehicle.

Main Methods:

  • Genetic engineering of Lactobacillus paracasei to express dsRNA targeting an essential C. elegans gene.
  • In vitro experiments to confirm dsRNA production and RNAi-induced gene silencing in C. elegans.
  • Assessment of L. paracasei as a potential carrier for oral dsRNA administration.

Main Results:

  • Successfully engineered L. paracasei to produce functional dsRNA.
  • Demonstrated RNAi-mediated silencing of an essential gene in C. elegans using the engineered bacteria.
  • Confirmed the potential of dsRNA-expressing L. paracasei for both in vitro assays and oral delivery.

Conclusions:

  • Engineered Lactobacillus paracasei provides a novel platform for dsRNA production and delivery.
  • This approach offers a promising strategy for gene silencing in C. elegans and potential therapeutic applications in mammals.
  • L. paracasei represents a versatile and safe carrier for RNAi-based interventions.