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Updated: Mar 14, 2026

Single Cell Transcriptional Profiling of Adult Mouse Cardiomyocytes
Published on: December 28, 2011
Data of methylome and transcriptome derived from human dilated cardiomyopathy
Bong-Seok Jo1, In-Uk Koh2, Jae-Bum Bae2
1Division of Biomedical Convergence, College of Biomedical Science, and Institute of Bioscience & Biotechnology, Kangwon National University, Chuncheon 24341, South Korea.
Human dilated cardiomyopathy (DCM) involves changes in DNA methylation and gene expression. This study identified specific DNA methylation and gene expression differences in the left ventricle, the heart chamber affected by DCM.
Area of Science:
- Genomics
- Molecular Biology
- Cardiovascular Science
Background:
- DNA methylation and gene expression alterations are linked to human dilated cardiomyopathy (DCM).
- The left ventricle (LV) is pathologically affected in DCM, while the right ventricle (RV) serves as a normal control.
- Understanding these molecular changes is crucial for DCM research.
Purpose of the Study:
- To identify differentially methylated probes (DMPs) and differentially expressed genes (DEGs) between the LV and RV in human DCM.
- To investigate alterations in DNA methylation within the regulatory regions of genes critical for left ventricle development.
Main Methods:
- Comparative analysis of DNA methylation patterns (methylome analysis) between pathological LV and control RV tissues.
- Gene expression profiling to identify differentially expressed genes (DEGs).
- Bioinformatics analysis to pinpoint DMPs and DEGs associated with DCM.
Main Results:
- Significant differences in DNA methylation were observed between the LV and RV.
- Specific genes showed altered expression levels correlating with methylation changes in the LV.
- Alterations were particularly noted in regulatory regions of genes involved in left ventricle development.
Conclusions:
- Epigenetic modifications, specifically DNA methylation changes, play a role in the pathogenesis of human dilated cardiomyopathy.
- These findings highlight potential molecular targets for understanding and treating DCM.
- The study provides valuable data for further research into the genetic and epigenetic underpinnings of DCM.
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