IP Library Granted Patent US 10,337,013
Granted Patent B2
US 10,337,013 · App. 15/684,234 · Granted Jul 2, 2019

Treatment of RNASE H1 related diseases by inhibition of natural antisense transcript to RNASE H1

Inventors: Joseph Collard (Delray Beach, FL); Olga Khorkova Sherman (Tequesta, FL)
Assignee: CuRNA, Inc.
C12N15/1137A61K31/7088C12N9/22C12N2310/11C12N2310/113C12N2310/14C12N2310/315C12N2310/321C12N2310/322Y02A50/409
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Quick Facts
Patent No.
US 10,337,013
App. No.
15/684,234
Granted
Jul 2, 2019
Kind
B2
Abstract

The present invention relates to antisense oligonucleotides that modulate the expression of and/or function of RNase H1, in particular, by targeting natural antisense polynucleotides of RNase H1. The invention also relates to the identification of these antisense oligonucleotides and their use in treating diseases and disorders associated with the expression of RNASE H1.

Claims (9)

1. A method of identifying and selecting at least one active modified antisense oligonucleotide of 10 to 30 nucleotides in length which specifically hybridizes to a natural antisense polynucleotide of a RNAse H1 gene and modulates expression of said RNAse H1 gene comprising: sequencing at least one natural antisense polynucleotide of the target RNAse H1 gene as a putative target; identifying at least one modified antisense oligonucleotide which is complementary to the natural antisense polynucleotide target; measuring the thermal melting point of a hybrid of said at least one modified antisense oligonucleotide and the target natural antisense polynucleotide under stringent hybridization conditions; and measuring the modulatory activity of said at least one modified oligonucleotide and selecting at least one active antisense oligonucleotide.

2. The method according to claim 1 wherein the RNAse H1 natural antisense polynucleotide comprises nucleotides 1 to 437 of SEQ ID NO: 2 or nucleotides 1 to 278 of SEQ ID NO: 3 or nucleotides 1 to 436 of SEQ ID NO: 4 or nucleotides 1 to 1140 of SEQ ID NO: 5; wherein said modified antisense oligonucleotide is 100% complementary to and specifically hybridizes to a complementary region of said natural antisense polynucleotides thereby modulating a function of and/or the expression of the RNase H1 polynucleotide in patient cells or tissues in vivo or in vitro.

3. The method according to claim 1 wherein the at least one antisense oligonucleotide is a siRNA.

4. The method according to claim 1 wherein the at least one antisense oligonucleotide is a single stranded, modified antisense oligonucleotide.

5. The method according to claim 4 wherein the modifications are selected from the group consisting of at least one modified sugar moiety; at least one modified internucleotide linkage; at least one modified nucleotide, and combinations thereof.

6. The method according to claim 5 wherein the at least one modified sugar moiety is selected from the group consisting of 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.

7. The method according to claim 5 wherein the at least one modified nucleotide is selected from the group consisting of peptide nucleic acids, locked nucleic acids (LNA), analogues, derivatives, and a combination thereof.

8. The method according to claim 5 wherein the least one modified internucleotide linkage is selected from the group consisting of phosphorothioate, alkylphosphonate, phosphorodithioate, alkylphosphonothioate, phosphoramidate, carbamate, carbonate, phosphate triester, acetamidate, carboxymethyl ester, and a combination thereof.

9. The method according to claim 1 wherein the antisense oligonucleotides are selected from the group consisting of SEQ ID NOS: 6 to 13.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 5, 2017
From: COLLARD, JOSEPH; KHORKOVA SHERMAN, OLGA
To: CURNA, INC.
Reel/Frame 043793/0263 →
Continuity (4)
Division 14573326 · Dec 17, 2014
Division 13575206
Provisional Application 61297878 · Jan 25, 2010
Related Publication 20170355996A1 · Dec 14, 2017
Cited By (1)
US 12,319,913