Inhibiting or downregulating glycogen synthase by creating premature stop codons using antisense oligonucleotides

Abstract

The present disclosure relates to antisense oligonucleotides (AONs) for modulating the expression of glycogen synthase. AONs of the present disclosure may be useful in treating diseases associated with the modulation of the expression of the enzyme glycogen synthase, such as Pompe disease. Also provided by the present disclosure are compositions comprising AONs, as well as methods of down regulating mRNA coding for glycogen synthase, methods for reducing glycogen synthase in skeletal and cardiac muscle, and methods for treating Pompe disease.

What is claimed is: 
     
         1 . A method of down regulating mRNA coding for glycogen synthase comprising administering an effective amount of an antisense oligonucleotide to an animal, wherein the antisense oligonucleotide comprises a sequence complementary to a nucleic acid sequence encoding for glycogen synthase, and wherein the hybridization of the antisense oligonucleotide to the nucleic acid sequence encoding for glycogen synthase induces exon skipping. 
     
     
         2 . The method of  claim 1 , wherein the antisense oligonucleotide is a PMO. 
     
     
         3 . The method of  claim 1 , wherein the antisense oligonucleotide is a PMO linked to a CPP. 
     
     
         4 . The method of  claim 1 , wherein the antisense oligonucleotide is selected from an oligonucleotide comprising subunits of one of Formula I-VI. 
     
     
         5 . The method of  claim 1 , wherein mRNA coding for glycogen synthase is reduced by 80%. 
     
     
         6 . The method of  claim 1 , wherein mRNA coding for glycogen synthase is reduced by 90%. 
     
     
         7 . The method of  claim 1 , wherein mRNA coding for glycogen synthase is reduced by 95%. 
     
     
         8 . The method of  claim 1 , wherein the effective amount ranges from 5 to 500 mg per dose. 
     
     
         9 . The method of  claim 1 , wherein the compound is administered intravenously. 
     
     
         10 . The method of  claim 1 , wherein the down regulation of mRNA coding for glycogen synthase occurs in skeletal and cardiac muscle. 
     
     
         11 . The method of  claim 1 , wherein the antisense oligonucleotide is at least 85% complementary to the nucleic acid sequence encoding for glycogen synthase. 
     
     
         12 . The method of  claim 1 , wherein the antisense oligonucleotide is at least 90% complementary to the nucleic acid sequence encoding for glycogen synthase. 
     
     
         13 . The method of  claim 1 , wherein the antisense oligonucleotide is at least 95% complementary to the nucleic acid sequence encoding for glycogen synthase. 
     
     
         14 . A method for reducing glycogen synthase in skeletal and cardiac muscle comprising administering to an animal an effective amount of an antisense oligonucleotide to an animal, wherein the antisense oligonucleotide comprises a sequence complimentary to a nucleic acid sequence encoding for glycogen synthase, and wherein the hybridization of the antisense oligonucleotide to the nucleic acid sequence encoding for glycogen synthase induces exon skipping. 
     
     
         15 . A method for treating Pompe disease comprising administering to an animal an effective amount of an antisense oligonucleotide to an animal, wherein the antisense oligonucleotide comprises a sequence complimentary to a nucleic acid sequence encoding for glycogen synthase, and wherein the hybridization of the antisense oligonucleotide to the nucleic acid sequence encoding for glycogen synthase induces exon skipping.