Single-stranded RNAi agents containing an internal, non-nucleic acid spacer
The instant disclosure features single-stranded RNA molecules comprising one or more internal, non-nucleotide spacers. A non-nucleotide spacer covalently links nucleotide portions of the molecule. The single-stranded RNA molecules function as guide or antisense strands that are capable of inhibiting gene expression via an RNA interference mechanism and, thus, represent single-stranded RNAi agents. The single-stranded RNAi molecules can be used in methods for a variety of therapeutic, diagnostic, target validation, genomic discovery, genetic engineering, and pharmacogenomic applications.
1. A single-stranded RNA molecule that mediates RNA interference against a target RNA, wherein said single-stranded RNA molecule comprises one or more internal, non-nucleotide spacer, wherein the non-nucleotide spacer comprises a C3-C6 alkyl.
2. The molecule of claim 1 , wherein the total number of nucleotides in the single-stranded RNA molecule is 8 to 26 nucleotides.
3. The molecule of claim 1 , wherein the target RNA comprises a target site that is within an untranslated region of the target RNA.
4. The molecule of claim 3 , wherein the single-stranded RNA molecule comprises at least 20 nucleotides that can base pair with the target site as the whole or as a part of a seed-targeted sequence of a naturally-occurring, endogenous miRNA nucleotide sequence.
5. The molecule of claim 4 , wherein the single-stranded RNA molecule is a single-stranded siRNA or the guide (antisense) strand of a duplex siRNA.
6. The molecule of claim 4 , wherein nucleotides in the single-stranded RNA molecule are at least 50% homologous to the naturally-occurring, endogenous miRNA nucleotide sequence.
7. The molecule of claim 1 , wherein the target RNA comprises a target site that is within a gene coding region of the target RNA.
8. The molecule of claim 1 , wherein nucleotides in the single-stranded RNA molecule are at least 90% complementary to a target site comprised by the target RNA.
9. The molecule of claim 1 , wherein at least one nucleotide of the single-stranded RNA molecule has a modified sugar.
10. The molecule of claim 1 , wherein at least one nucleotide of the single-stranded RNA molecule has a modified internucleotide linkage.
11. The molecule of claim 1 , having a terminal cap at the 5′-end, the 3′-end, or both the 5′- and 3′-ends.
12. The molecule of claim 1 , having a terminal group at the 5′-end, the 3′-end, or both the 5′- and 3′-ends.
13. The molecule of claim 12 , wherein the terminal group is a ligand.
14. The molecule of claim 13 , wherein the ligand is a ligand for a cellular receptor.
15. The molecule of claim 14 , wherein the ligand is a carbohydrate.
16. The molecule of claim 15 , wherein the carbohydrate is an N-acetyl-D-galactosamine.
17. A composition comprising the single-stranded RNA molecule of claim 1 and a pharmaceutically acceptable carrier.
18. The composition of claim 17 , further comprising a liposome, a hydrogel, a cyclodextrin, a biodegradable nanocapsule, a bioadhesive microsphere, or a proteinaceous vector.
19. A method of reducing the expression of an endogenous RNA target gene in a cell, comprising contacting the cell with the composition of claim 17 .
20. The molecule of claim 1 , wherein the single-stranded RNA molecule comprises a nucleic acid portion comprising a first nucleotide portion (N1) and a second nucleotide portion (N2), wherein N1 comprises one nucleotide or a contiguous stretch of nucleotides and N2 comprises one nucleotide or a contiguous stretch of nucleotides, wherein the one or more internal, non-nucleotide spacer (S1) covalently links N1 and N2, wherein the single-stranded RNA molecule comprises the following structure: 5′ N1-S1-N2 3′.
21. The molecule of claim 20 , wherein N1 comprises 18 contiguous nucleotides, 19 contiguous nucleotides, or 20 contiguous nucleotides.
22. The molecule of claim 20 , wherein N2 comprises 2 contiguous nucleotides or 1 nucleotide.