Three component chimeric antisense oligonucleotides
This invention relates to antisense oligonucleotides that target mRNAs in cells as substrates for the cellular enzyme RNase H and thereby cause specific degradation of the targeted mRNA. The oligonucleotides have three components: an RNase H activating region, a complementary region and 3′ and 5′ ends. The invention optimizes each of the components to resist intracellular nucleases, to increase hybridization to target mRNA, to specifically inactivate target mRNA in cells, and to decrease cytotoxicity.
1. A chimeric antisense oligonucleotide comprising: a 5′ terminus; a 3′ terminus and from II to 59 5′→3′-linked nucleotides which contiguously hybridize to specific RNA and which are independently selected from the group consisting of 2′-modified phosphodiester nucleotides, and 2′-modified P-alkyloxyphosphotriester nucleotides; and wherein said 11 to 59 5′→3′-linked nucleotides are divided by an RNase H-activating region capable of contiguously hybridizing to the specific RNA and of between three and ten contiguous phosphorothioate-linked deoxyribonucleotides, and wherein the 3′ terminus of said oligonucleotide is drawn from the group consisting of: an inverted deoxyribonucleotide, a contiguous stretch of one to three phosphorothioate 2′-modified ribonucleotides, a biotin group, and a P-alkyloxyphosphodiester nucleotide, and wherein the 5′ terminus of said oligonucleotide is drawn from the group consisting of: an inverted deoxyribonucleotide, a contiguous stretch of one to three phosphorothioate 2′-modified ribonucleotides, a biotin group, and a P-alkyloxyphosphodiester nucleotide.
2. The oligonucleotide of claim 1 , provided the 3′ terminus is not blocked by a 3′→3′ phosphorothioate linked nucleotide.
3. The oligonucleotide of claim 1 , in which the 3′ terminus is blocked by a moiety comprising a 3′→3′ phosphorothioate linked nucleotide.
4. The oligonucleotide of claim 1 , in which the 3′ terminus is blocked by a moiety comprising a 3′→3′ phosphodiester linked nucleotide.
5. The oligonucleotide of claim 4 , in which the 3′ most 5′→3′ internucleotide linkage is a phosphorothioate linkage or a P-ethoxyphosphotriester linkage.
6. The oligonucleotide of claim 4 , in which the 5′ most 5′→3′ internucleotide linkage is a phosphorothioate linkage or a P-ethoxyphosphotriester linkage.
7. The oligonucleotide of claim 1 , in which the 3′ terminal nucleoside and the 5′ most nucleotide are 2′-modified nucleotides.
8. The oligonucleotide of claim 7 , in which the 5′ most 5′→3′ internucleotide linkage is a phosphorothioate linkage or a P-ethoxyphosphotriester linkage.
9. The oligonucleotide of claim 8 , in which the two 5′ most 5′→3′ internucleotide linkages are independently either a phosphorothioate linkage or a P-ethoxyphosphotriester linkage.
10. The oligonucleotide of claim 8 , in which all phosphorothioate linkages are contiguous with the 3′ most 5′→3′ internucleotide linkage.
11. The oligonucleotide of claim 10 , in which the 2′-modified nucleotide is a 2′-methoxy or 2′-fluoro nucleotide.
12. The oligonucleotide of claim 10 , which comprises at least thirteen 2′-methoxy phosphodiester nucleotides.
13. The oligonucleotide of claim 10 , having between 15 and 50 nucleotides.
14. The oligonucleotide of claim 13 , which comprises at least eight 2′-methoxy phosphodiester nucleotides.
15. The oligonucleotide of claim 13 , which comprises at least thirteen 2′-methoxy phosphodiester nucleotides.
16. The oligonucleotide of claim 1 , in which the 2′-modified nucleotides are selected from the group consisting of 2′-fluoro and 2′-methoxy nucleotides.
17. The oligonucleotide of claim 1 , in which there are no 2′-modified phosphorothioate nucleotides.
18. A method of specifically cleaving an RNA in a cell Containing RNase H which comprises administering an effective amount of an oligonucleotide complementary to the RNA comprising: a 5′ terminus; a 3′ terminus; and from 11 to 59 5′→3′-linked nucleotides which contiguously hybridize to the RNA and which are independently selected from the group consisting of 2′-modified phosphodiester nucleotides, 2′-modified P-alkyloxyphosphotriester nucleotides; and wherein said 11 to 59 5′→3′-linked nucleotides are divided by an RNase H-activating region which contiguously hybridizes to the RNA and comprises between three and ten contiguous phosphorothioate-linked deoxyribonucleotides, and wherein the 3′ terminus of said oligonucleotide is drawn from the group consisting of: an inverted deoxyribonucleotide, a contiguous stretch of one to three phosphorothioate deoxyribonucleotides, phosphorothioate 2′-modified ribonucleotides, a biotin group, and a P-alkyloxyphosphodiester-linked nucleotide, and wherein the 5′ terminus of said oligonucleotide is drawn from the group consisting of: an inverted deoxyribonucleotide, a contiguous stretch of one to three phosphorothioate deoxyribonucleotides, phosphorothioate 2′-modified ribonucleotides, a biotin group, and a P-alkyloxyphosphodiester-linked nucleotide.
19. A chimeric antisense oligonucleotide comprising:
a) an RNase H activation region which contiguously hybridizes to a specific RNA and which has between 5 and 10 contiguous deoxyphosphorothioate nucleotides;
b) between 4 to contiguous 5′→3′-linked 2′-methoxyribonucleotides which contiguously hybridize to the specific RNA; and
c) an exonuclease blocking group present at the 3′ end, the 5′ end, or both the 3′ and 5′ ends of the oligonucleotide drawn from the group consisting of: a non-5′→3′ phosphodiester-linked nucleotide, from one to three contiguous 5′→3′-linked modified nucleotides, and a non-nucleotide chemical blocking group.