Modified oligonucleotides targeting SNPs

Patent metadata

Field	Value
Publication number	US-11827882-B2
Application number	US-201916537374-A
Country	US
Kind code	B2
Filing date	Aug 9, 2019
Priority date	Aug 10, 2018
Publication date	Nov 28, 2023
Grant date	Nov 28, 2023

Abstract

Novel oligonucleotides that enhance silencing of the expression of a gene containing a single nucleotide polymorphism (SNP) relative to the expression of the corresponding wild-type gene are provided. Methods of using novel oligonucleotides that enhance silencing of the expression of a gene containing a SNP relative to the expression of the corresponding wild-type gene are provided.

First claim

The invention claimed is:

1. A di-branched oligonucleotide compound comprising two RNAs, wherein the RNAs are connected to one another by one or more moieties selected from a linker, a spacer and a branching point, wherein each RNA has a 5′ end, a 3′ end and a seed region, wherein each RNA is complementary to a region of a gene comprising an allelic polymorphism, and wherein each RNA comprises:
a single nucleotide polymorphism (SNP) position nucleotide at a position within the seed region, the SNP position nucleotide being complementary to the allelic polymorphism; and
a mismatch (MM) position nucleotide located 2-11 nucleotides from the SNP position nucleotide that is a mismatch with a nucleotide in the gene.

2. A di-branched oligonucleotide compound comprising two or more nucleic acid sequences, wherein the nucleic acid sequences (N) are connected to one another by one or more moieties selected from a linker (L), a spacer (S) and optionally a branching point (B),
wherein each nucleic acid sequence is double-stranded and comprises a sense strand and an antisense strand, wherein the sense strand and the antisense strand each have a 5′ end and a 3′ end, wherein the sense strand and the antisense strand each comprises one or more chemically-modified nucleotides,
wherein each antisense strand has a seed region, wherein each antisense strand is complementary to a region of a gene comprising an allelic polymorphism, and wherein each antisense strand comprises:
a single nucleotide polymorphism (SNP) position nucleotide at a position within the seed region, the SNP position nucleotide being complementary to the allelic polymorphism; and
a mismatch (MM) position nucleotide located 2-11 nucleotides from the SNP position nucleotide that is a mismatch with a nucleotide in the gene.

3. The di-branched oligonucleotide compound claim 1 , wherein the RNA further comprises at least one vinyl phosphonate modification in an intersubunit linkage having the formula:

optionally wherein a vinyl phosphonate motif is inserted next to the SNP position nucleotide or next to the MM position nucleotide.

4. The di-branched oligonucleotide compound of claim 1 , wherein the di-branched oligonucleotide compound has an hsi-RNA structure.

5. The di-branched oligonucleotide compound of claim 1 , wherein the SNP position nucleotide is complementary to an allelic polymorphism of an htt SNP selected from the group consisting of rs363125, rs362273, rs362307, rs362336, rs362331, rs362272, rs362306, rs362268, rs362267, and rs363099.

6. The di-branched oligonucleotide of claim 1 , wherein each RNA is an ASO or a double-stranded RNA (dsRNA).

7. The di-branched oligonucleotide compound of claim 1 , wherein the region of a gene comprising the allelic polymorphism comprises a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-10.

8. The di-branched oligonucleotide compound of claim 1 , further comprising at least one 5′ stabilizing moiety selected from the group consisting of phosphate, vinyl phosphonate, C5-methyl (R or S or racemic), C5-methyl on vinyl, and reduced vinyl.

9. The di-branched oligonucleotide compound of claim 1 , further comprising at least one conjugate moiety selected from the group consisting of alkyl chain, vitamin, peptide, glycosphingolipid, polyunsaturated fatty acid, secosteroid, steroid hormone, and steroid lipid.

10. The di-branched oligonucleotide compound of claim 2 , wherein the RNA further comprises at least one vinyl phosphonate modification in an intersubunit linkage having the formula:

optionally wherein a vinyl phosphonate motif is inserted next to the SNP position nucleotide or next to the MM position nucleotide.

11. The di-branched oligonucleotide compound of claim 2 , wherein the sense strands and the antisense strands each comprise >80% chemically-modified nucleotides.

12. The di-branched oligonucleotide compound of claim 2 , wherein the nucleotides at positions 1 and 2 from the 5′ end of the sense and antisense strands are connected to adjacent nucleotides via phosphorothioate linkages.

13. The di-branched oligonucleotide compound of claim 2 , wherein each antisense strand comprises at least 15 contiguous nucleotides, and wherein each sense strand comprises at least 15 contiguous nucleotides and has complementarity to the antisense strand.

14. The di-branched oligonucleotide compound of claim 2 , wherein the compound further comprises a hydrophobic moiety attached to the terminal 5′position of the branched oligonucleotide compound.

15. The di-branched oligonucleotide compound of claim 2 , wherein each double-stranded nucleic acid sequence is independently connected to a linker, spacer or branching point at the 3′ end or at the 5′ end of the sense strand or the antisense strand.

16. The di-branched oligonucleotide compound of claim 2 , wherein the SNP position nucleotide is complementary to an allelic polymorphism of an htt SNP selected from the group consisting of rs363125, rs362273, rs362307, rs362336, rs362331, rs362272, rs362306, rs362268, rs362267, and rs363099.

17. The di-branched oligonucleotide compound of claim 1 , wherein the region of a gene comprising the allelic polymorphism comprises a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-10.

18. The di-branched oligonucleotide compound of claim 1 , further comprising at least one 5′ stabilizing moiety selected from the group consisting of phosphate, vinyl phosphonate, C5-methyl (R or S or racemic), C5-methyl on vinyl, and reduced vinyl.

19. A method of inhibiting expression of a gene comprising an allelic polymorphism in a cell, the method comprising contacting the cell with the di-branched oligonucleotide compound of claim 1 .

20. A method of inhibiting expression of a gene comprising an allelic polymorphism in a cell, the method comprising contacting the cell with the di-branched oligonucleotide compound of claim 2 .

Assignees

• Univ Massachusetts

Inventors

• Khvorova Anastasia
• Alterman Julia
• Conroy Faith
• Pfister Edith
• Aronin Neil
• Yamada Ken

Classifications

• A61K31/7115

  Nucleic acids or oligonucleotides having modified bases, i.e. other than adenine, guanine, cytosine, uracil or thymine · CPC title

• C12N15/113 Primary

  Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; {Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing (when used in plants C12N15/8218)} · CPC title

• C12N15/85

  for animal cells · CPC title

• C12N2310/14

  interfering nucleic acids [NA] · CPC title

• C12N2310/312

  Phosphonates · CPC title