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Updated: Apr 8, 2026

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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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Long non-coding RNA profiling of hypertrophic cardiomyopathy in mice
Graham A Branscom1, Michael P Morley2, Jonathan J Herrera3
1Cardiology Division, Department of Medicine, University of Pennsylvania, Philadelphia, PA, USA. graham.branscom@icahn.mssm.edu.
Scientific Data
|April 6, 2026
Summary
Long non-coding RNAs (lncRNAs) are key regulators in cellular processes. This study identifies differentially expressed lncRNAs in a mouse model of hypertrophic cardiomyopathy (HCM), offering insights into disease mechanisms.
Area of Science:
- Genomics
- Molecular Biology
- Cardiovascular Research
Background:
- Long non-coding RNAs (lncRNAs) are crucial regulators of gene expression.
- Hypertrophic cardiomyopathy (HCM) is a prevalent inherited heart condition.
- The role of lncRNAs in HCM pathophysiology is currently unknown.
Purpose of the Study:
- To investigate the role of lncRNAs in the development of hypertrophic cardiomyopathy.
- To identify differentially expressed lncRNAs in a mouse model of HCM.
- To provide a resource for studying lncRNA function in human HCM.
Main Methods:
- RNA sequencing (RNA-Seq) was performed on left ventricle samples from transgenic HCM TNNT2 ∆160 mice and non-transgenic controls.
- Differential expression analysis was conducted to identify dysregulated lncRNAs.
- Mouse lncRNA genes with human orthologs were identified.
Main Results:
- A dataset of differentially expressed lncRNAs was generated from HCM mouse models.
- Specific lncRNAs were found to be dysregulated in the context of HCM.
- A list of mouse lncRNAs with human orthologs was compiled.
Conclusions:
- lncRNAs are likely involved in the pathophysiology of hypertrophic cardiomyopathy.
- This study provides a valuable dataset for further research into lncRNA function in HCM.
- The identified human orthologs facilitate translational studies for human HCM.

