Abstract
Background: RNAi technology is widely used to downregulate specific gene products. Investigating the phenotype induced by downregulation of gene products provides essential information about the function of the specific gene of interest. When RNAi is applied in Drosophila melanogaster or Caenorhabditis elegans, often large dsRNAs are used. One of the drawbacks of RNAi technology is that unwanted gene products with sequence similarity to the gene of interest can be down regulated too. To verify the outcome of an RNAi experiment and to avoid these unwanted off-target effects, an additional non-overlapping dsRNA can be used to down-regulate the same gene. However it has never been tested whether this approach is sufficient to reduce the risk of off-targets.
Methodology: We created a novel tool to analyse the occurance of off-target effects in Drosophila and we analyzed 99 randomly chosen genes.
Principal Findings: Here we show that nearly all genes contain non-overlapping internal sequences that do show overlap in a common off-target gene.
Conclusion: Based on our in silico findings, off-target effects should not be ignored and our presented on-line tool enables the identification of two RNA interference constructs, free of overlapping off-targets, from any gene of interest.
Original language | English |
---|---|
Article number | 13119 |
Number of pages | 7 |
Journal | PLoS ONE |
Volume | 5 |
Issue number | 10 |
DOIs | |
Publication status | Published - 1-Oct-2010 |
Keywords
- MESSENGER-RNA
- LONG DSRNAS
- HUMAN-CELLS
- INTERFERENCE
- DROSOPHILA
- MICRORNAS
- NUCLEUS
- SCREENS
- SIRNA
- MIRNA