Reducing off-target effects in RNA interference experiments

In this article, Dr. Christian Nievera, senior product manager at Horizon Discovery, discusses how to minimize non-specific effects of siRNA reagents

27 Oct 2021
Blake Forman
Content Creator

Industry news

The success of functional genomic studies using RNA interference (RNAi) technology can be limited by non-specific effects of the siRNA reagents. ON-TARGETplus™ siRNA reagents from Dharmacon™ are designed to knock down the target gene with minimal off-target effects. You can use these reagents in your gene silencing experiments to reduce the presence of off-target phenotypes without jeopardizing on-target gene knockdown, writes Dr. Christian Nievera, senior product manager for RNAi and functional genomics screening libraries at Horizon Discovery.

The use of small interfering RNAs (siRNAs) for silencing gene expression has become an invaluable tool in numerous fields of scientific research. However, experiments using this technology can be complicated by off-target effects, manifesting as measurable phenotypes such as false positives. These non-specific effects are difficult to predict and analyze and can confound the interpretation of experimental data.

Scientists from Dharmacon have recognized this issue, we have extensively reviewed the evidence relating to off-target effects. Three strategies have been identified that are proven to improve the specificity of siRNA effects. These three strategies are incorporated into the Dharmacon ON-TARGETplus siRNA reagents to ensure cleaner experimental results in loss-of-function assays.

1. Pool siRNAs

Off-target effects are reduced when a lower concentration of siRNA is used. However, reducing the concentration would normally be associated with a depletion of target gene knockdown. Dharmacon offers a simple solution: SMARTpool siRNA reagents pool four highly functional SMARTselection-designed siRNAs targeting the same gene. Using SMARTpool siRNA considerably reduces the off-target profile without sacrificing target-specific knockdown.

2. Chemically modify siRNAs

Scientists at Dharmacon have identified a unique combination of modifications that eliminate as much as 80% of the off-target activity. These chemical modifications reduce both sense and antisense strand off-target effects while preserving on-target knockdown.

3. Apply design filters

Certain siRNA design features, such as the presence of multiple 3’ UTR seed matches, have been associated with the likelihood of a gene being off-targeted. The use of novel rational design filters, incorporating an understanding of features known to affect the specificity of siRNA binding, has enabled Dharmacon to optimize its siRNA reagents. ON-TARGETplus siRNA reagents have been developed using pooling strategies, chemical modifications, and design filters to reduce off-target activity versus unmodified siRNA without jeopardizing on-target gene knockdown.

Avoid unintended gene modulation and have confidence in the specificity of your RNAi by using ON-TARGETplus siRNA reagents in your functional genomic studies.

For more information on siRNA reagents from Dharmacon, contact Horizon Discovery >>

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Genome AnalysisGenomics, the study of genomes, includes functional genomics, evolutionary genomics and comparative genomics. There are many genomic technologies such as DNA sequencing of whole genomes, computational biology and bioinformatics. DNA and nucleic acids must be isolated and concentrated from cells for analysis with kits, automated analyzers and software. Other useful technologies for studying genomics include PCR, microarrays and electrophoresis.Gene Expression and Molecular CloningMolecular cloning is a set of techniques that utilizes vectors to transfer recombinant DNA into host cells and is an essential tool for investigating the expression of genes and proteins in bacterial or mammalian cells. A variety of vectors optimized for gene cloning and expression in a range of host organisms are available, alongside competent cells for genetic replication. Here, you can explore a range of molecular tools, high-quality genomic and cDNA libraries, premade clones, transformation and transfection reagents and mutagenesis or gene expression detection assays and expression arrays. Find the best gene expression and molecular cloning products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.RNA InterferenceRNA interference (RNAi) uses siRNA or miRNA for transcriptional silencing, gene knockdown and regulation of gene expression. RNAi requires chemical synthesis, introduction of DNA vectors into cells, an assay of RNAi effects and RNAi quantification or analysis. Consider target sequence selection, reagent preparation, controls, high specificity and effectiveness and low non-specific gene knockdown.siRNAGene EditingGene editing is the precise alteration to an organism's DNA, with CRISPR being the most well-known technique. It is used in a wide range of applications, including the development of disease models and gene therapy, and crop improvement. Browse our peer-reviewed product directory to find the best gene editing solutions, compare products, check reviews, and get pricing directly from manufacturers.GenomicsGenomics is the study of genomes, focusing on the sequencing, analysis, and interpretation of genetic material. It is key in understanding genetic diseases, evolutionary biology, and personalized medicine. Techniques like next-generation sequencing (NGS) are commonly used in genomics research. Browse our peer-reviewed product directory to find the best genomics tools, compare products, check reviews, and get pricing directly from manufacturers.Assay DevelopmentThe process of proving an assay to be sensitive with respect to the target is known as assay development. The assay should be able to characterize novel compounds and measure the potency of these compounds against a validated biological target.