| Literature DB >> 16964256 |
Meghana M Kulkarni1, Matthew Booker, Serena J Silver, Adam Friedman, Pengyu Hong, Norbert Perrimon, Bernard Mathey-Prevot.
Abstract
To evaluate the specificity of long dsRNAs used in high-throughput RNA interference (RNAi) screens performed at the Drosophila RNAi Screening Center (DRSC), we performed a global analysis of their activity in 30 genome-wide screens completed at our facility. Notably, our analysis predicts that dsRNAs containing > or = 19-nucleotide perfect matches identified in silico to unintended targets may contribute to a significant false positive error rate arising from off-target effects. We confirmed experimentally that such sequences in dsRNAs lead to false positives and to efficient knockdown of a cross-hybridizing transcript, raising a cautionary note about interpreting results based on the use of a single dsRNA per gene. Although a full appreciation of all causes of false positive errors remains to be determined, we suggest simple guidelines to help ensure high-quality information from RNAi high-throughput screens.Entities:
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Year: 2006 PMID: 16964256 DOI: 10.1038/nmeth935
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547