Reduction of off-target RNA interference toxicity
The present invention is directed to RNA interference (RNAi) molecules targeted against a nucleic acid sequence, and methods of using these RNAi molecules to reduce off-target toxicity.
1. A nucleic acid encoding an artificial primary miRNA transcript (pri-miRNA) consisting of, in order of position, a 5′-flanking region, a first siRNA region, a loop region, a second siRNA region, and a 3′-flanking region, wherein the 5′-flanking region comprises:
(a) a 5′-joining sequence contiguously linked to the first siRNA region, wherein the 5′-joining sequence consists of 5-7 nucleotides;
(b) a 5′-bulge sequence positioned upstream from the 5′-joining sequence, wherein the 5′-bulge sequence consists of 1-10 nucleotides;
(c) a 5′-spacer sequence positioned upstream from the 5′-bulge sequence, wherein the 5′-spacer sequence consists of 10-12 nucleotides; and
(d) a 5′-upstream sequence positioned upstream from the 5′-spacer sequence, wherein the 5′-upstream sequence is about 30-2000 nucleotides in length;
and wherein the 3′-flanking region comprises:
(e) a 3′-joining sequence contiguously linked to the first siRNA region, wherein the 3′-joining sequence consists of 5-7 nucleotides;
(f) a 3′-bulge sequence positioned downstream from the 3′-joining sequence; wherein the 3′-bulge sequence consists of 1-10 nucleotides;
(g) a 3′-spacer sequence positioned downstream from the 3′-bulge sequence, wherein the 3′-spacer sequence consists of 10-12 nucleotides; and
(h) a 3′-downstream sequence positioned downstream from the 3′-spacer sequence, wherein the 3′-downstream sequence is about 30-2000 nucleotides in length.
2. The nucleic acid of claim 1 , wherein the 5′-flanking region is contiguously linked to the first siRNA region, the loop region is positioned between the first siRNA region and the second siRNA region, and the second siRNA region is contiguously linked to the 3′-flanking region.
3. The nucleic acid of claim 1 , wherein the first siRNA region is a non-guide region and the second siRNA region is a guide region.
4. The nucleic acid of claim 1 , wherein the first siRNA region is a guide region and the second siRNA region is a non-guide region.
5. The nucleic acid of claim 1 , wherein the 5′-joining sequence encodes GUGASSS, wherein S is either a G or C nucleotide.
6. The nucleic acid of claim 1 , wherein the 5′-bulge sequence comprises a cloning site.
7. The nucleic acid of claim 1 , wherein the 5′-bulge sequence encodes UAAACUCGA.
8. The nucleic acid of claim 1 , wherein the 3′-joining sequence is at least about 85% complementary to the 5′-joining sequence.
9. The nucleic acid of claim 1 , wherein the 3′-joining sequence encodes CGCYUAC, wherein Y is C or U.
10. The nucleic acid of claim 1 , wherein the 3′-bulge sequence comprises a cloning site.
11. The nucleic acid of claim 1 , wherein the 5′-bulge sequence is complementary to the 3′-bulge sequence at only one nucleotide at each end of the bulge sequence.
12. The nucleic acid of claim 1 , wherein the 3′-spacer sequence is at least about 70% complementary to the 5′-spacer sequence.
13. The nucleic acid of claim 1 , wherein the 5′-upstream sequence pairs with less than 20% of the 3′-downstream sequence.
14. The nucleic acid of claim 1 , wherein the loop region is from 15-19 nucleotides in length.
15. The nucleic acid of claim 14 , wherein the loop region is 17 nucleotides in length.
16. The nucleic acid of claim 1 , wherein the loop region encodes CUNNNNNNNNNNNNNNNNGG (SEQ ID NO: 182), CCNNNNNNNNNNNNNNNGG (SEQ ID NO: 183), CUGUGAAGCCACAGAUGGG (SEQ ID NO: 184) or CCGUGAAGCCACAGAUGGG (SEQ ID NO: 185).
17. An RNA encoded by nucleic acid of claim 1 .
18. An expression cassette comprising a promoter contiguously linked to the nucleic acid of claim 1 .