Treatment of Sirtuin (SIRT) related diseases by inhibition of natural antisense transcript to a Sirtuin (SIRT)
The present invention relates to antisense oligonucleotide that modulate the expression of and/or function of a Sirtuin (SIRT), in particular, by targeting natural antisense polynucleotides of a Sirtuin (SIRT). The invention also relates to the identification of these antisense oligonucleotides and their use in treating diseases and disorders associated with the expression of Sirtuins (SIRT)s.
1. A synthetic, modified, single-stranded oligonucleotide of 18 to 30 nucleotides in length comprising at least one modification wherein the at least one modification is selected from: at least one modified sugar moiety; at least one modified internucleotide linkage; at least one modified nucleotide, and combinations thereof; wherein said oligonucleotide is an antisense compound which is 100% complementary to and specifically hybridizes to a natural antisense polynucleotide of a Sirtuin (SIRT) 2, 3, 4, 5 or 7 gene and upregulates the function and/or expression of a Sirtuin (SIRT) in vivo or in vitro as compared to a normal control, wherein the natural antisense polynucleotide is selected from the group consisting of SEQ ID NOs: 17, 18, 19, 20 or 23, wherein:
(a) the natural antisense polynucleotide is SEQ ID NO: 17 and the synthetic, modified oligonucleotide comprises a nucleotide sequence selected from the group consisting of SEQ ID NO: 96;
(b) the natural antisense polynucleotide is SEQ ID NO: 18 and the synthetic, modified oligonucleotide comprises a nucleotide sequence selected from the group consisting of SEQ ID NOs: 100 and 102;
(c) the natural antisense polynucleotide is SEQ ID NO: 19 and the synthetic, modified oligonucleotide comprises a nucleotide sequence selected from the group consisting of SEQ ID NO: 105;
(d) the natural antisense polynucleotide is SEQ ID NO: 20 and the synthetic, modified oligonucleotide comprises a nucleotide sequence selected from the group consisting of SEQ ID NOs: 108 and 109; or
(e) the natural antisense polynucleotide is SEQ ID NO: 23 and the synthetic, modified oligonucleotide comprises a nucleotide sequence selected from the group consisting of SEQ ID NOs: 122-125.
2. The oligonucleotide of claim 1 , wherein the at least one modification comprises an internucleotide linkage selected from the group consisting of: phosphorothioate, alkylphosphonate, phosphorodithioate, alkylphosphonothioate, phosphoramidate, carbamate, carbonate, phosphate triester, acetamidate, carboxymethyl ester, and combinations thereof.
3. The oligonucleotide of claim 1 , wherein said oligonucleotide comprises at least one phosphorothioate internucleotide linkage.
4. The oligonucleotide of claim 1 , wherein said oligonucleotide comprises a backbone of phosphorothioate internucleotide linkages.
5. The oligonucleotide of claim 1 , wherein the oligonucleotide comprises at least one modified nucleotide, said modified nucleotide selected from: a peptide nucleic acid, a locked nucleic acid (LNA), and a combination thereof.
6. The oligonucleotide of claim 1 , wherein the oligonucleotide comprises a plurality of modifications, wherein said modifications comprise modified nucleotides selected from: phosphorothioate, alkylphosphonate, phosphorodithioate, alkylphosphonothioate, phosphoramidate, carbamate, carbonate, phosphate triester, acetamidate, carboxymethyl ester, and a combination thereof.
7. The oligonucleotide of claim 1 , wherein the oligonucleotide comprises a plurality of modifications, wherein said modifications comprise modified nucleotides selected from: peptide nucleic acids, locked nucleic acids (LNA), and a combination thereof.
8. The oligonucleotide of claim 1 , wherein the oligonucleotide comprises at least one modified sugar moiety selected from: a 2′-O-methoxyethyl modified sugar moiety, a 2′-methoxy modified sugar moiety, a 2′-O-alkyl modified sugar moiety, a bicyclic sugar moiety, and a combination thereof.
9. The oligonucleotide of claim 1 , wherein the oligonucleotide comprises a plurality of modifications, wherein said modifications comprise modified sugar moieties selected from: a 2′-O-methoxyethyl modified sugar moiety, a 2′-methoxy modified sugar moiety, a 2′-O-alkyl modified sugar moiety, a bicyclic sugar moiety, and a combination thereof.
10. A modified oligonucleotide of 19-21 nucleotides in length, wherein the modified oligonucleotide comprises a nucleotide sequence selected from the group consisting of SEQ ID NOs: 96, 100, 102, 104-109 and 122 to 125.
11. A pharmaceutical composition comprising one or more modified oligonucleotides according to claim 10 and a pharmaceutically acceptable excipient.
12. The pharmaceutical composition of claim 11 , wherein the one or more modified oligonucleotides comprises one or more modifications or substitutions selected from phosphorothioates, modified sugar moieties, methylphosphonate, peptide nucleic acid, locked nucleic acid (LNA) molecules, and combinations thereof.
13. The modified oligonucleotide of claim 10 , wherein the modified oligonucleotide comprises one or more modifications or substitutions selected from phosphorothioate, locked nucleic acid (LNA) molecules, and combinations thereof.
14. A modified oligonucleotide of 14-27 nucleotides in length, wherein the modified oligonucleotide comprises a nucleotide sequence selected from the group consisting of SEQ ID NOs: 126 or 127.
15. The modified oligonucleotide according to claim 14 , wherein the modified oligonucleotide comprises one or more modifications selected from the group consisting of a phosphorothioate, methylphosphonate, peptide nucleic acid, locked nucleic acid (LNA) molecules, and combinations thereof.
16. A pharmaceutical composition comprising the modified oligonucleotide according to claim 14 .
17. A pharmaceutical composition comprising one or more modified oligonucleotides according to claim 1 and a pharmaceutically acceptable excipient.