Whole-genome thermodynamic analysis reduces siRNA off-target effects

PLoS One. 2013;8(3):e58326. doi: 10.1371/journal.pone.0058326. Epub 2013 Mar 6.

Abstract

Small interfering RNAs (siRNAs) are important tools for knocking down targeted genes, and have been widely applied to biological and biomedical research. To design siRNAs, two important aspects must be considered: the potency in knocking down target genes and the off-target effect on any nontarget genes. Although many studies have produced useful tools to design potent siRNAs, off-target prevention has mostly been delegated to sequence-level alignment tools such as BLAST. We hypothesize that whole-genome thermodynamic analysis can identify potential off-targets with higher precision and help us avoid siRNAs that may have strong off-target effects. To validate this hypothesis, two siRNA sets were designed to target three human genes IDH1, ITPR2 and TRIM28. They were selected from the output of two popular siRNA design tools, siDirect and siDesign. Both siRNA design tools have incorporated sequence-level screening to avoid off-targets, thus their output is believed to be optimal. However, one of the sets we tested has off-target genes predicted by Picky, a whole-genome thermodynamic analysis tool. Picky can identify off-target genes that may hybridize to a siRNA within a user-specified melting temperature range. Our experiments validated that some off-target genes predicted by Picky can indeed be inhibited by siRNAs. Similar experiments were performed using commercially available siRNAs and a few off-target genes were also found to be inhibited as predicted by Picky. In summary, we demonstrate that whole-genome thermodynamic analysis can identify off-target genes that are missed in sequence-level screening. Because Picky prediction is deterministic according to thermodynamics, if a siRNA candidate has no Picky predicted off-targets, it is unlikely to cause off-target effects. Therefore, we recommend including Picky as an additional screening step in siRNA design.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Validation Study

MeSH terms

  • Gene Knockdown Techniques / methods*
  • Gene Targeting / methods*
  • Genetic Engineering / methods*
  • Genome / genetics*
  • Humans
  • Inositol 1,4,5-Trisphosphate Receptors / genetics
  • Isocitrate Dehydrogenase / genetics
  • Predictive Value of Tests
  • RNA, Small Interfering / genetics*
  • Repressor Proteins / genetics
  • Thermodynamics
  • Tripartite Motif-Containing Protein 28

Substances

  • ITPR2 protein, human
  • Inositol 1,4,5-Trisphosphate Receptors
  • RNA, Small Interfering
  • Repressor Proteins
  • Isocitrate Dehydrogenase
  • IDH1 protein, human
  • TRIM28 protein, human
  • Tripartite Motif-Containing Protein 28

Grants and funding

This work is supported by National Science Foundation grant DBI-0850195. http://www.nsf.gov/awardsearch/showAward.do?AwardNumber=0850195 NSF had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.