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1000 Titel
  • Four Dimensions of the Cardiac Myocyte Epigenome: from Fetal to Adult Heart
1000 Autor/in
  1. Rommel, Carolin |
  2. Hein, Lutz |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-03-19
1000 Erschienen in
1000 Quellenangabe
  • 22(5):26
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s11886-020-01280-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082379/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Purpose of review!#!Development, physiological growth and the response of the heart to injury are accompanied by changes of the transcriptome and epigenome of cardiac myocytes. Recently, cell sorting and next generation sequencing techniques have been applied to determine cardiac myocyte-specific transcriptional and epigenetic mechanisms. This review provides a comprehensive overview of studies analysing the transcriptome and epigenome of cardiac myocytes in mouse and human hearts during development, physiological growth and disease.!##!Recent findings!#!Adult cardiac myocytes express > 12,600 genes, and their expression levels correlate positively with active histone marks and inversely with gene body DNA methylation. DNA methylation accompanied the perinatal switch in sarcomere or metabolic isoform gene expression in cardiac myocytes, but remained rather stable in heart disease. DNA methylation and histone marks identified > 100,000 cis-regulatory regions in the cardiac myocyte epigenome with a dynamic spectrum of transcription factor binding sites. The ETS-related transcription factor ETV1 was identified as an atrial-specific element involved in the pathogenesis of atrial fibrillation. Thus, dynamic development of the atrial vs. ventricular cardiac myocyte epigenome provides a basis to identify location and time-dependent mechanisms of epigenetic control to shape pathological gene expression during heart disease. Identifying the four dimensions of the cardiac myocyte epigenome, atrial vs. ventricular location, time during development and growth, and disease-specific signals, may ultimately lead to new treatment strategies for heart disease.
1000 Sacherschließung
lokal Ventricular cardiac myocytes
lokal Adult [MeSH]
lokal Transcription factor
lokal Humans [MeSH]
lokal Heart/growth
lokal Animals [MeSH]
lokal Atrial cardiac myocytes
lokal Fetal Heart/physiology [MeSH]
lokal Epigenesis, Genetic/physiology [MeSH]
lokal Mice [MeSH]
lokal Regenerative Medicine (SM Wu, Section Editor)
lokal Transcriptome
lokal Myocytes, Cardiac/metabolism [MeSH]
lokal Epigenetics
lokal DNA methylation
lokal Epigenesis, Genetic/genetics [MeSH]
lokal Gene Expression Regulation [MeSH]
lokal Heart Ventricles [MeSH]
lokal Epigenome [MeSH]
lokal Topical Collection on Regenerative Medicine
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/Um9tbWVsLCBDYXJvbGlu|https://frl.publisso.de/adhoc/uri/SGVpbiwgTHV0eg==
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1000 Erstellt am 2023-11-18T12:02:37.566+0100
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