Allele-specific RNA interference
Human diseases caused by dominant, gain-of-function mutations develop in heterozygotes bearing one mutant and one wild-type copy of a gene. Because the wild-type gene often performs important functions, whereas the mutant gene is toxic, any therapeutic strategy must selectively inhibit the mutant while retaining wild-type gene expression. The present invention includes methods of specifically inhibiting the expression of a mutant allele, while preserving the expression of a co-expressed wild-type allele using RNAi, a therapeutic strategy for treating genetic disorders associated with dominant, gain-of-function gene mutations. The invention also includes small interfering RNAs (siRNAs) and small hairpin RNAs (shRNAs) that selectively suppress mutant, but not wild-type, expression of copper zinc superoxide dismutase (SOD1), which causes inherited amyotrophic lateral sclerosis (ALS). The present invention further provides asymmetric siRNAs and shRNAs with enhanced efficacy and specificity and mediating RNAi.
1. A method of inhibiting expression of a target allele in a cell comprising at least two different alleles of a gene, the method comprising (i) introducing to the cell shRNA comprising a duplex stem comprising an antisense stem portion having a length of 21 nucleotides and a sense stem portion, wherein said shRNA is targeted to the target allele, and wherein the target allele is a gain-of-function mutant allele, and (ii) enhancing the asymmetry of said stem, wherein the asymmetry is enhanced by lessening the base pair strength between base pairs at the 5′ end of the antisense strand portion and corresponding base pairs in the 3′ end of the sense stem portion, wherein the base pair strength is less due to introduction of a single mismatched base pair between the 5′ end of the antisense stem portion and the 3′ end of the sense stem portion at position 3 from the 5′ end of the antisense strand portion.
2. The method of claim 1 , wherein said shRNA is expressed in the cell from a construct.
3. The method of claim 1 , where said shRNA is introduced to the cell by contacting said cell with said shRNA.
4. The method of claim 1 , wherein the allele is correlated with a disorder associated with a dominant gain-of-function mutation.
5. The method of claim 4 , wherein the disorder is selected from the group of amyotrophic lateral sclerosis, Huntington's disease, Alzheimer's disease, and Parkinson's disease.
6. The method of claim 5 , wherein the disorder is amyotrophic lateral sclerosis.
7. The method of claim 6 , wherein the allele is SOD1.
8. The method of claim 1 , wherein the allele comprises a point mutation.
9. The method of claim 8 , wherein the point mutation is a guanine:cytosine mutation.
10. The method of claim 8 , wherein the allele is SOD1.
11. The method of claim 10 , wherein the mutation is G256C.
12. The method of claim 10 , wherein the mutation is G281C.
13. A method of treating a subject having a disorder correlated with the presence of a dominant gain of function mutant allele, the method comprising administering to the subject a therapeutically effective amount of an shRNA or a construct encoding said shRNA, wherein said shRNA comprises (i) a duplex stem comprising an antisense stem portion having a length of 21 nucleotides and a sense stem portion, wherein said shRNA is targeted to a gain-of-function mutant allele, and (ii) wherein said stem is asymmetric and the asymmetry is enhanced by lessening the base pair strength between base pairs at the 5′ end of the antisense strand portion and corresponding base pairs in the 3′ end of the sense stem portion, wherein the base pair strength is less due to introduction of a single mismatched base pair between the 5′ end of the antisense stem portion and the 3′ end of the sense stem portion at position 3 from the 5′ end of the antisense strand portion.
14. The method of claim 13 , wherein said shRNA is expressed in a cell of said subject from said construct encoding said shRNA.
15. The method of claim 13 , wherein said shRNA is introduced to a cell of the subject by contacting said cell with said shRNA.
16. The method of claim 13 , wherein the disorder is selected from the group of amyotrophic lateral sclerosis, Huntington's disease, Alzheimer's disease, and Parkinson's disease.
17. The method of claim 16 , wherein the disorder is the disease is amyotrophic lateral sclerosis.
18. The method of claim 17 , wherein the allele is SOD1.
19. The method of claim 13 , wherein the allele comprises a point mutation.
20. The method of claim 19 , wherein the point mutation is a guanine:cytosine mutation.
21. The method of claim 19 , wherein the allele is SOD1.
22. The method of claim 21 , wherein the mutation is G256C.
23. The method of claim 21 , wherein the mutation is G281C.