Triggered RNAi
The present application relates to methods and compositions for triggering RNAi. Triggered RNAi is highly versatile because the silencing targets are independent of the detection targets. In some embodiments, methods of silencing or modulating the expression of a marker gene are provided. The methods generally comprise providing an initiator to a cell comprising a detection target and a silencing target gene, wherein the detection target is different from the silencing target gene, wherein binding of the detection target to the initiator initiates formation of an inactivator double-stranded RNA (inactivator dsRNA). The inactivator dsRNA can silence the silencing target gene to modulate the expression of a marker gene.
1. A method of detecting the presence of a detection target by modulating the expression of a marker gene, the method comprising:
providing an initiator to a cell, wherein the cell comprises a detection target, a silencing target gene, and a marker gene, wherein the detection target is different from the silencing target gene, wherein the initiator comprises a nucleic acid sequence comprising a) a detection binding region that binds to the detection target and b) an initiator region;
providing a first substrate monomer to the cell, wherein the first substrate monomer comprises a silencing target complement region that is substantially complementary to a portion of the silencing target gene, and an initiator complement region, wherein the initiator complement region hybridizes to the initiator region; and
providing a second substrate monomer to the cell, wherein the second substrate monomer comprises a silencing target region that is substantially complementary to the silencing target complement region, wherein binding of the detection target to the initiator initiates hybridization of the silencing target complement region of the first substrate monomer to the silencing target region of the second substrate monomer and formation of an inactivator double-stranded RNA (inactivator dsRNA) which silences the silencing target gene, and wherein said silencing of the silencing target gene modulates the expression of said marker gene;
determining the level of expression of said marker gene; and
assessing whether said maker gene is expressed at a level that is different than a predetermined level, thereby detecting the presence of said detection target.
2. The method of claim 1 , wherein upon binding of the detection target to the initiator, a portion of the initiator is made available to bind to the initiator complement region of the first substrate monomer.
3. The method of claim 2 , wherein upon binding of the initiator complement region to the initiator, the silencing target complement region is made available to bind to the silencing target region of the first substrate monomer.
4. The method of claim 3 , wherein upon binding of the silencing target region to the silencing target complement region, the inactivator dsRNA is formed.
5. The method of claim 1 , wherein the initiator comprises an RNA hairpin monomer.
6. The method of claim 1 , wherein the nucleic acid sequence comprises a conformation-switching aptamer.
7. The method of claim 1 , wherein the first substrate monomer is an RNA hairpin.
8. The method of claim 1 , wherein the second substrate monomer is an RNA hairpin.
9. The method of claim 1 , further comprising: contacting the cell with at least one accessory molecule comprising a nucleic acid sequence that binds to a region flanking the initiator binding site of the detection target.
10. The method of claim 1 , wherein the initiator region is able to bind to the initiator complement region when a detection target is present in the cell.
11. The method of claim 1 , wherein the inactivator dsRNA can be processed by Dicer.
12. The method of claim 11 , wherein the inactivator dsRNA can be processed to produce a 19 bp duplex with 2-nt 3′ overhangs.
13. The method of claim 11 , wherein the inactivator dsRNA comprises a RNA duplex substrate from about 19 base pairs to about 22 base pairs in length.
14. The method of claim 1 , wherein the inactivator dsRNA is an siRNA.
15. The method of claim 14 , wherein the inactivator dsRNA is a 19 bp duplex with 2-nt 3′ overhangs.
16. The method of claim 1 , wherein the marker gene is GFP.
17. The method of claim 1 , wherein the detection target is a nucleic acid.
18. The method of claim 17 , wherein the silencing target gene is an mRNA comprising a sequence different from the sequence of the detection target.
19. The method of claim 1 , wherein the detection target is associated with a disease or disorder.
20. The method of claim 19 , wherein the detection target is an mRNA associated with a cancer.
21. The method of claim 19 , wherein the detection target is a viral nucleic acid.
22. The method of claim 19 , wherein the detection target is an mRNA molecule associated with a disease or disorder.
23. The method of claim 1 , wherein the silencing target gene is an mRNA.
24. The method of claim 1 , wherein the silencing target gene comprises said marker gene.
25. The method of claim 1 , wherein the silencing target gene comprises a nucleic acid sequence that modulates the expression of said marker gene.
26. The method of claim 1 , wherein the initiator comprises a recognition molecule such that upon binding of the recognition molecule to the detection target, a portion of the initiator is made available to bind to the initiator complement region of the first substrate monomer.
27. The method of claim 26 , wherein the recognition molecule is an aptamer.
28. The method of claim 26 , wherein the detection target is a nucleic acid.
29. The method of claim 26 , wherein the detection target is selected from the group consisting of polypeptides, carbohydrates, lipids and small molecules.
30. A method of detecting the presence of a detection target by modulating the expression of a marker gene, the method comprising:
contacting a cell with an initiator, wherein the cell comprises a detection target, a silencing target gene, and a marker gene, wherein the initiator comprises a nucleic acid sequence comprising a detection target binding region, an initiator region, and a silencing target complement region, wherein the detection target binding region can interact with the detection target, and wherein the detection target is different from the silencing target gene; and
contacting the cell with a substrate monomer comprising a nucleic acid that is at least partially double stranded, wherein the substrate monomer comprises an initiator complement region that is complementary to the initiator region of the initiator and a silencing target region that is complementary to the silencing target complement region, wherein an inactivator double-stranded RNA (inactivator dsRNA) is formed by hybridization of the silencing target complement region to the silencing target region subsequent to interaction of the detection target to the detection target binding region, wherein the inactivator dsRNA silences the silencing target gene, and wherein said silencing of the silencing target gene modulates the expression of said marker gene;
determining the level of expression of said marker gene; and
assessing whether said maker gene is expressed at a level that is different than a predetermined level, thereby detecting the presence of said detection target.