Antisense oligonucleotides and their use for treating Pendred syndrome
The present disclosure relates to the field of medicine. In particular, it relates to novel antisense oligonucleotides that prevent or reduce exon 8 skipping in the SLC26A4 gene during pre-mRNA splicing, and their use in the treatment of Pendred Syndrome.
1. A chemically modified antisense oligonucleotide of 10-30 nucleotides in length comprising all or a portion of SEQ ID NO:1 (5′-tgtattagtactaagaggaacacca-3′), wherein the antisense oligonucleotide is:
a. HUA0003-1027
(SEQ ID NO: 2)
(5′-tagtactaagaggaacac-3′);
b. HUA0003-1029
(SEQ ID NO: 3)
(5′-attagtactaagaggaacac-3′);
c. HUA0003-1030
(SEQ ID NO: 4)
(5′-tattagtactaagaggaacac-3′);
d. HUA0003-1031
(SEQ ID NO: 5)
(5′-gtattagtactaagaggaacac-3′);
e. HUA0003-1032
(SEQ ID NO: 6)
(5′-tgtattagtactaagaggaacac-3′);
f. HUA0003-0930
(SEQ ID NO: 7)
(5′-tattagtactaagaggaacacc-3′);
g. HUA0003-0929
(SEQ ID NO: 8)
(5′-attagtactaagaggaacacc-3′);
h. HUA0003-0928
(SEQ ID NO: 9)
(5′-ttagtactaagaggaacacc-3′);
or
i. HUA0003-0931
(SEQ ID NO: 10)
(5′-gtattagtactaagaggaacacc-3′).
2. The antisense oligonucleotide of claim 1 , wherein the antisense oligonucleotide comprises a non-natural backbone.
3. The antisense oligonucleotide of claim 2 , wherein the non-natural backbone comprises modified sugar moieties.
4. The antisense oligonucleotide of claim 3 , wherein the modified sugar moieties comprise 2′-O-methoxyethyl ribose.
5. The antisense oligonucleotide of claim 2 , wherein the non-natural backbone comprises modified phosphates.
6. The antisense oligonucleotide of claim 5 , wherein the modified phosphates comprise phosphorothioates.
7. The antisense oligonucleotide of claim 1 , wherein the antisense oligonucleotide comprises modified nitrogenous bases.
8. The antisense oligonucleotide of claim 7 , wherein the modified nitrogenous bases comprise 5-methylcytosine bases.
9. The antisense oligonucleotide of claim 1 further comprising a pharmaceutically acceptable carrier or excipient.
10. A method of preventing or reducing exon 8 skipping in the SLC26A4 gene during pre-mRNA splicing, comprising introducing a nucleic acid molecule into a cell, wherein the nucleic acid molecule is an antisense oligonucleotide comprising all or a portion of SEQ ID NO:1 (5′-tgtattagtactaagaggaacacca-3′), wherein the oligonucleotide hybridizes to an intron 8 target region of the SLC26A4 gene, and wherein the oligonucleotide prevents or reduces exon 8 skipping during pre-mRNA splicing of the SLC26A4 gene.
11. The method of claim 10 , wherein the antisense oligonucleotide is:
a. HUA0003-1027
(SEQ ID NO: 2)
(5′-tagtactaagaggaacac-3′);
b. HUA0003-1029
(SEQ ID NO: 3)
(5′-attagtactaagaggaacac-3′);
c. HUA0003-1030
(SEQ ID NO: 4)
(5′-tattagtactaagaggaacac-3′);
d. HUA0003-1031
(SEQ ID NO: 5)
(5′-gtattagtactaagaggaacac-3′);
e. HUA0003-1032
(SEQ ID NO: 6)
(5′-tgtattagtactaagaggaacac-3′);
f. HUA0003-0930
(SEQ ID NO: 7)
(5′-tattagtactaagaggaacacc-3′);
g. HUA0003-0929
(SEQ ID NO: 8)
(5′-attagtactaagaggaacacc-3′);
h. HUA0003-0928
(SEQ ID NO: 9)
(5′-ttagtactaagaggaacacc-3′);
or
i. HUA0003-0931
(SEQ ID NO: 10)
(5′-gtattagtactaagaggaacacc-3′).
12. The method of claim 10 , wherein the cell is an animal cell.
13. The method of claim 12 , wherein the cell is a human cell.
14. The method of claim 10 , wherein the nucleic acid molecule is introduced into a cell by way of an expression vector.
15. The method of claim 14 , wherein the expression vector is a pCI-neo expression vector.
16. A method of treating hearing loss in a subject in a subject having Pendred syndrome comprising administering a therapeutically effective amount of the antisense oligonucleotide of claim 1 .
17. The method of claim 16 , wherein the antisense oligonucleotide is administered via parenteral administration.