Position-specific chemical modification of siRNAs reduces “off-target” transcript silencing

AL Jackson, J Burchard, D Leake, A Reynolds… - Rna, 2006 - rnajournal.cshlp.org
AL Jackson, J Burchard, D Leake, A Reynolds, J Schelter, J Guo, JM Johnson, L Lim…
Rna, 2006rnajournal.cshlp.org
Transfected siRNAs regulate numerous transcripts sharing limited complementarity to the
RNA duplex. This unintended (“off-target”) silencing can hinder the use of RNAi to define
gene function. Here we describe position-specific, sequence-independent chemical
modifications that reduced silencing of partially complementary transcripts by all siRNAs
tested. Silencing of perfectly matched targets was unaffected by these modifications. The
chemical modification also reduced off-target phenotypes in growth inhibition studies. Key to …
Transfected siRNAs regulate numerous transcripts sharing limited complementarity to the RNA duplex. This unintended (“off-target”) silencing can hinder the use of RNAi to define gene function. Here we describe position-specific, sequence-independent chemical modifications that reduced silencing of partially complementary transcripts by all siRNAs tested. Silencing of perfectly matched targets was unaffected by these modifications. The chemical modification also reduced off-target phenotypes in growth inhibition studies. Key to the modification was 2′-O-methyl ribosyl substitution at position 2 in the guide strand, which reduced silencing of most off-target transcripts with complementarity to the seed region of the siRNA guide strand. The sharp position dependence of 2′-O-methyl ribosyl modification contrasts with the broader position dependence of base-pair substitutions within the seed region, suggesting a role for position 2 of the guide strand distinct from its effects on pairing to target transcripts.
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