Methods and compositions for treating gain-of-function disorders using RNA interference
AssigneeUniversity of Massachusetts
InventorsZuoshang Xu, Xugang Xia
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Abstract
The present invention relates to novel methods for treating dominant gain-of-function diseases. The invention provides methods for targeting regions of the copper zinc superoxide dismutase (SOD1), which causes inherited amyotrophic lateral sclerosis (ALS), with RNAi agent. The invention further provides RNAi resistant replacement genes containing mismatches with their respective RNAi agents. The invention also provides for vectors that express RNAi agent and RNAi resistant replacement gene of the present invention.
Claims14
A method of inhibiting expression of a human SOD1 gain-of-function target mRNA, and providing for expression of a RNAi resistant replacement gene in a cell comprising administering to the cell a nucleic acid agent comprising a first polynucleotide sequence encoding an RNAi agent specific for the human SOD1 gain-of-function target mRNA, and a second polynucleotide sequence encoding a RNAi resistant replacement gene,
- wherein the RNAi agent comprises an antisense strand having sufficient sequence complementarity to the human SOD1 gain-of-function target mRNA to induce cleavage of the target mRNA, and a sense strand complementary to said antisense strand, and
- wherein the RNAi replacement gene comprises a nucleotide sequence encoding human SOD1 and wherein the RNAi replacement gene comprises SEQ ID NO:3 or SEQ ID NO:85,
- whereby expression of the human SOD1 gain-of-function target mRNA is inhibited and expression of the RNAi resistant replacement gene is achieved.
A method of inhibiting expression of a human SOD1 gain-of function target mRNA in a cell, comprising administering to the cell a RNAi agent comprising an antisense strand having sufficient sequence complementarity to RNAi the human SOD1 gain-of-function target mRNA to induce cleavage of the target mRNA, and a sense strand complementary to said antisense strand, said cell expressing an RNAi resistant replacement gene, wherein the RNAi replacement gene comprises a nucleotide sequence encoding human SOD1 and wherein the RNAi replacement gene comprises SEQ ID NO:3 or SEQ ID NO:85,
- whereby expression of the human SOD1 gain-of-function target mRNA is inhibited and expression of the RNAi resistant replacement gene is achieved.
A method of treating a subject having a disorder correlated with presence of a human SOD1 dominant gain-of-function target mRNA, the method comprising administering to the subject a therapeutically effective amount of a nucleic acid agent comprising a first polynucleotide sequence encoding an RNAi agent specific for the human SOD1 gain-of-function target mRNA, and a second polynucleotide sequence encoding a RNAi resistant replacement gene,
- wherein the RNAi agent comprises an antisense strand having sufficient sequence complementarity to the human SOD1 gain-of-function target mRNA to induce cleavage of the target mRNA, and a sense strand complementary to said antisense strand, and
- wherein the RNAi replacement gene comprises a nucleotide sequence encoding human SOD1 and wherein the RNAi replacement gene comprises SEQ ID NO:3 or SEQ ID NO:85, thereby treating the disease in a subject.
Dependencies are inferred from the claim text.