Modified siRNA structure with a single nucleotide bulge overcomes conventional siRNA-mediated off-target silencing.

Mol Ther

Department of Chemistry, Global Research Laboratory for RNAi Medicine, Sungkyunkwan University, Suwon, Korea.

Published: September 2011

AI Article Synopsis

  • Off-target gene silencing is a significant issue in RNA interference, primarily caused by imperfect matching of siRNA with unintended mRNA targets.
  • Researchers developed "bulge-siRNA," which features a special bulge in the antisense strand, enhancing its ability to distinguish between correctly matched and mismatched targets without affecting the silencing of intended targets.
  • Genome-wide analysis indicated that bulge-siRNAs reduced off-target silencing more effectively than previously used chemical modifications, positioning it as a promising alternative for improving siRNA specificity.

Article Abstract

Off-target gene silencing is a major concern when using RNA interference. Imperfect pairing of the antisense strand with unintended mRNA targets is one of the main causes of small interfering RNA (siRNA) off-target silencing. To overcome this, we have developed "bulge-siRNA," a modified siRNA backbone structure with a single nucleotide (nt) bulge placed in the antisense strand. We found that siRNAs with a bulge at position 2 of the antisense strand were able to discriminate better between perfectly matched and mismatched targets, with no loss in silencing of the intended target. Genome-wide analysis also revealed that the bulge-siRNAs significantly reduced off-target silencing of transcripts with complementarity to the seed region of the siRNA antisense strand. When compared to 2'-methoxy ribosyl (2'-OMe) modified siRNAs previously developed to alleviate antisense off-target silencing; the bulge modification could better discriminate between on- versus off-targets. Our results suggest that the bulge-siRNA structure is a simple, yet superior alternative to chemical modifications for minimizing off-target silencing triggered by conventional siRNA structures.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182346PMC
http://dx.doi.org/10.1038/mt.2011.109DOI Listing

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