RNA interference for the treatment of gain-of-function disorders
The present invention relates to the discovery of an effective treatment for a variety of gain-of-function diseases, in particular, Huntington's disease (HD). The present invention utilizes RNA Interference technology (RNAi) against polymorphic regions in the genes encoding various gain-of-function mutant proteins resulting in an effective treatment for the gain-of-function disease.
1. A composition for treating or managing Huntington's disease, comprising an RNA silencing agent targeting UAAGAGAUGGGGACAGUACUUCAACGCUAGAAGAACA (SEQ ID NO: 43) of an Htt mRNA, such that RNA silencing of said mRNA occurs, wherein the RNA silencing agent comprises:
(i) an antisense strand or a variant thereof having sufficient complementarity to SEQ ID NO: 43 to direct target-specific cleavage or translational repression of the Htt mRNA;
(ii) a sense strand or a variant thereof that is substantially complementary to the antisense strand; and
(iii) wherein the sense and antisense strands are capable of annealing together.
2. The composition of claim 1 , wherein the RNA silencing agent comprises an engineered RNA precursor.
3. The composition of claim 2 , wherein the engineered RNA precursor is expressed by a vector.
4. The composition of claim 3 , wherein the vector comprises a viral vector, retroviral vector, expression cassette, or plasmid.
5. The composition of claim 3 , wherein the vector further comprises an RNA Polymerase III or RNA Polymerase II promoter.
6. The composition of claim 5 , wherein the RNA Polymerase III promoter comprises a U6 or H1 promoter.
7. The composition of claim 3 , wherein the engineered RNA precursor comprises at least one internal bulge.
8. The composition of claim 2 , wherein each strand of the engineered RNA precursor is between 15 and 50 base pairs in length.
9. The composition of claim 1 , wherein the RNA silencing agent is conjugated to a lipophilic moiety optionally comprising a cholesterol moiety.