IP Library Granted Patent US 12,286,626
Granted Patent B2
US 12,286,626 · App. 17/283,845 · Granted Apr 29, 2025

Myocardial enhancer RNA and methods of use

Inventors: Ching-Pin Chang (Indianapolis, IN); Wei Cheng (Indianapolis, IN)
Assignee: THE TRUSTEES OF INDIANA UNIVERSITY
C12N15/113C12Q1/6883C12N2310/14
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Quick Facts
Patent No.
US 12,286,626
App. No.
17/283,845
Granted
Apr 29, 2025
Kind
B2
Abstract

Disclosed are methods of detecting myocardial enhancer RNA levels in mammalian cardiomyocytes. In a further embodiment, a method of disrupting assembly of an enhancer DNA-Myh6 promoter-Myh7 promoter complex, is provided wherein the method comprises providing enhancer RNA to a cardiomyocyte.

Claims (17)

1. A method of treating a patient at risk for heart disease comprising:

administering a therapeutically effective amount of an RNA sequence to the patient, wherein the RNA sequence comprises a sequence having at least 95% sequence identity to SEQ ID NO: 2 or its corresponding DNA equivalent thereof.

2. The method of claim 1 , wherein the heart disease is hypertrophy.

3. The method of claim 1 , further comprising decreasing Brg1 activity.

4. The method of claim 3 , wherein the Brg1 activity is decreased by administering an interfering RNA to silence the translation of Brg1.

5. The method of claim 1 , further comprising analyzing Uhrt levels after the step of administering the RNA.

6. The method of claim 1 , wherein treating the patient comprises inhibiting assembly of a complex of an enhancer DNA (eDNA) with Myh6 promoter-Myh7 promoter in a cardiomyocyte cell by increasing binding of Uhrt to the eDNA, wherein the eDNA comprises a sequence having at least 95% sequence identity with SEQ ID NO: 3.

7. The method of claim 6 , wherein the administration increases the concentration of Uhrt RNA and decreases the concentration of eDNA relative to a cell into which the Uhrt RNA and the eDNA was not introduced.

8. The method of claim 1 , wherein administering the RNA sequence comprising a sequence having at least 95% sequence identity to SEQ ID NO: 2 or a corresponding DNA equivalent thereof prevents a stress-induced Myh6-to-Myh7 switch.

9. The method of claim 1 , wherein the heart disease is heart failure.

10. The method of claim 1 , wherein the RNA sequence comprises a sequence having at least 96% sequence identity to SEQ ID NO: 2 or its corresponding DNA equivalent thereof.

11. The method of claim 1 , wherein the RNA sequence comprises a sequence having at least 97% sequence identity to SEQ ID NO: 2 or its corresponding DNA equivalent thereof.

12. The method of claim 1 , wherein the RNA sequence comprises a sequence having at least 98% sequence identity to SEQ ID NO: 2 or its corresponding DNA equivalent thereof.

13. The method of claim 1 , wherein the RNA sequence comprises a sequence having at least 99% sequence identity to SEQ ID NO: 2 or its corresponding DNA equivalent thereof.

14. The method of claim 1 , wherein the RNA sequence comprises SEQ ID NO: 2 or its corresponding DNA equivalent thereof.

15. The method of claim 1 , wherein the RNA sequence comprises SEQ ID NO: 2.

16. The method of claim 1 , wherein the RNA sequence consists of SEQ ID NO: 2.

Assignments (2)
CONFIRMATORY LICENSE Recorded Dec 4, 2023
From: INDIANA UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 065762/0619 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2021
From: CHANG, CHING-PIN; CHENG, WEI
To: THE TRUSTEES OF INDIANA UNIVERSITY
Reel/Frame 055872/0473 →
Continuity (2)
Provisional Application 62747732 · Oct 19, 2018
Related Publication 20210380977A1 · Dec 9, 2021
References Cited (11)
US 20050214835A1 · Bristow et al. · 2005 [cited by applicant]
US 20160114004A1 · Chang · 2016 [cited by examiner]
WO WO2010006215A1 · 2010 [cited by examiner]
ABSS SEQ ID No. 2 query, retrieved Jan. 15, 2024 (Year: 2024). [cited by examiner]
GenomeMYH7 (MYH7 Genomic Data Viewer, https://www.ncbi.nlm.nih.gov/gdv/browser/gene/?id=4625, retrieved Jul. 10, 2024) (Year: 2024). [cited by examiner]
GenBank3 (GenBank3, Human chromosome 14 DNA sequence BAC C-2201G16 of library CalTech-D from chromosome 14 of [cited by examiner]
GenBankEnhancer ( [cited by examiner]
PCT International Search Report and Written Opinion completed by the ISA/US on Feb. 8, 2020 and issued in connection with PCT/US2019/056995. [cited by applicant]
GenBank AL132855.4, Human chromosome 14 DNA sequence BAG C-2201G16 of library CalTech-D from chromosome 14 of [cited by applicant]
GenBank AC157212, Mus musculus BAC clone RP23-171A13 from chromosome 14, complete sequence, Apr. 27, 2005 (Apr. 27, 2005). [Retrieved on Feb. 8, 2020]. Retrieved from the Internet <URL: https://www.ncbi.nlm.nih.gov/nucc… [cited by applicant]
Qin et al. “Localization of human cardiac beta-myosin heavy chain gene (MYH7) to chromosome 14q12 by in situ hybridization” Cytogenet Cell Genet, 1990, vol. 54, p. 74-76; abstract. [cited by applicant]