IP Library Patent Application 14700311
Patent Application
App. No. 14/700,311

METHODS FOR MODULATING RNA USING 5' TARGETING OLIGONUCLEOTIDES

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
14/700,311
Abstract

Aspects of the invention relate to methods for increasing gene expression in a targeted manner. In some embodiments, methods and compositions are provided that are useful for posttranscriptionally altering protein and/or RNA levels in a targeted manner. Aspects of the invention disclosed herein provide methods and compositions that are useful for protecting RNAs from degradation (e.g., exonuclease mediated degradation).

Claims (26)

1 . A method of increasing gene expression in a cell, the method comprising:

delivering to a cell an oligonucleotide comprising the general formula 5′-X 1 -X 2 -3′, wherein X 1 comprises 5 to 20 nucleotides that have a region of complementarity that is complementary with at least 5 contiguous nucleotides of an RNA transcript encoded by the gene, wherein the nucleotide at the 3′-end of the region of complementary of X 1 is complementary with the nucleotide at the transcription start site of the RNA transcript; and X 2 comprises 1 to 20 nucleotides.

2 . The method of claim 1 , wherein the RNA transcript has a 7-methylguanosine cap at its 5′-end.

3 . The method of claim 1 , wherein the RNA transcript has a 7-methylguanosine cap, and wherein the nucleotide at the 3′-end of the region of complementary of X 1 is complementary with the nucleotide of the RNA transcript that is immediately internal to the 7-methylguanosine cap.

4 . The method of claim 1 , wherein at least the first nucleotide at the 5′-end of X 2 is a pyrimidine complementary with guanine.

5 . The method of claim 2 , wherein the second nucleotide at the 5′-end of X 2 is a pyrimidine complementary with guanine.

6 . The method of claim 1 , wherein X 2 comprises the formula 5′-Y 1 -Y 2 -Y 3 -3′, wherein X 2 forms a stem-loop structure having a loop region comprising the nucleotides of Y 2 and a stem region comprising at least two contiguous nucleotides of Y 1 hybridized with at least two contiguous nucleotides of Y 3 .

7 . The method of claim 6 , wherein Y 1 , Y 2 and Y 3 independently comprise 1 to 10 nucleotides.

8 . The method of claim 6 , wherein Y 3 comprises, at a position immediately following the 3′-end of the stem region, a pyrimidine complementary with guanine.

9 . The method of claim 4 , wherein the pyrimidine complementary with guanine is cytosine.

10 - 13 . (canceled)

14 . The method of claim 1 , wherein the RNA transcript is an mRNA, non-coding RNA, long non-coding RNA, miRNA, or snoRNA.

15 . (canceled)

16 . The method of claim 1 , wherein the RNA transcript is an mRNA and the delivery results in an increase in the level of a protein encoded by the mRNA.

17 - 28 . (canceled)

29 . The method of claim 1 , wherein the oligonucleotide is 10 to 50 nucleotide in length.

30 - 32 . (canceled)

33 . The method of claim 1 , wherein the oligonucleotide comprises at least one modified internucleoside linkage.

34 . The method of claim 1 , wherein the oligonucleotide comprises at least one modified nucleotide.

35 . The method of claim 1 , wherein at least one nucleotide of the oligonucleotide comprises a 2′ O-methyl.

36 . The method of claim 1 , wherein the oligonucleotide comprises at least one ribonucleotide, at least one deoxyribonucleotide, at least one 2′-fluoro-deoxyribonucleotides or at least one bridged nucleotide.

37 . The method of claim 36 , wherein the bridged nucleotide is a LNA nucleotide, a cEt nucleotide or a ENA modified nucleotide.

38 . The method of claim 1 , wherein each nucleotide of the oligonucleotide is a LNA nucleotide.

39 . The oligonucleotide of claim 1 , wherein the nucleotides of the oligonucleotide comprise alternating deoxyribonucleotides and 2′-fluoro-deoxyribonucleotides, 2′-O-methyl nucleotides, or bridged nucleotides.

40 . The method of claim 1 , wherein the oligonucleotide is a mixmer.

41 - 155 . (canceled)

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 29, 2015
From: OZSOLAK, FATIH
To: RANA THERAPEUTICS, INC.
Reel/Frame 035744/0395 →