Off-target effects by siRNA can induce toxic phenotype (original) (raw)

  1. Yuriy Fedorov,
  2. Emily M. Anderson,
  3. Amanda Birmingham,
  4. Angela Reynolds,
  5. Jon Karpilow,
  6. Kathryn Robinson,
  7. Devin Leake,
  8. William S. Marshall, and
  9. Anastasia Khvorova
  10. Dharmacon Research, Lafayette, Colorado 80026, USA

Abstract

Although recent microarray studies have provided evidence of RNA interference (RNAi)-mediated off-target gene modulation, little is known about whether these changes induce observable phenotypic outcomes. Here we show that a fraction of randomly selected small inhibitory RNAs (siRNAs) can induce changes in cell viability in a target-independent fashion. The observed toxicity requires an intact RNAi pathway and can be eliminated by the addition of chemical modifications that reduce off-target effects. Furthermore, an analysis of toxic and nontoxic duplexes identifies a strong correlation between the toxicity and the presence of a 4-base-pair motif (UGGC) in the RISC-entering strand of toxic siRNA. This article provides further evidence of siRNA-induced off-target effects generating a measurable phenotype and also provides an example of how such undesirable phenotypes can be mitigated by addition of chemical modifications to the siRNA.

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