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Transcriptional and Epigenetic Regulation of Cardiac Electrophysiology

Spatiotemporal gene expression during cardiac development is a highly regulated process. Activation of key signaling pathways involved in electrophysiological programming, such as Notch and Wnt signaling, occurs in early cardiovascular development and these pathways are reactivated during pathologic...

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Detalles Bibliográficos
Autores principales: Jimenez, Jesus, Rentschler, Stacey L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6785575/
https://www.ncbi.nlm.nih.gov/pubmed/31346662
http://dx.doi.org/10.1007/s00246-019-02160-w
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author Jimenez, Jesus
Rentschler, Stacey L.
author_facet Jimenez, Jesus
Rentschler, Stacey L.
author_sort Jimenez, Jesus
collection PubMed
description Spatiotemporal gene expression during cardiac development is a highly regulated process. Activation of key signaling pathways involved in electrophysiological programming, such as Notch and Wnt signaling, occurs in early cardiovascular development and these pathways are reactivated during pathologic remodeling. Direct targets of these signaling pathways have also been associated with inherited arrhythmias such as Brugada syndrome and arrhythmogenic cardiomyopathy. In addition, evidence is emerging from animal models that reactivation of Notch and Wnt signaling during cardiac pathology may predispose to acquired arrhythmias, underscoring the importance of elucidating the transcriptional and epigenetic effects on cardiac gene regulation. Here, we highlight specific examples where gene expression dictates electrophysiological properties in both normal and diseased hearts.
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spelling pubmed-67855752019-10-17 Transcriptional and Epigenetic Regulation of Cardiac Electrophysiology Jimenez, Jesus Rentschler, Stacey L. Pediatr Cardiol Riley Symposium Spatiotemporal gene expression during cardiac development is a highly regulated process. Activation of key signaling pathways involved in electrophysiological programming, such as Notch and Wnt signaling, occurs in early cardiovascular development and these pathways are reactivated during pathologic remodeling. Direct targets of these signaling pathways have also been associated with inherited arrhythmias such as Brugada syndrome and arrhythmogenic cardiomyopathy. In addition, evidence is emerging from animal models that reactivation of Notch and Wnt signaling during cardiac pathology may predispose to acquired arrhythmias, underscoring the importance of elucidating the transcriptional and epigenetic effects on cardiac gene regulation. Here, we highlight specific examples where gene expression dictates electrophysiological properties in both normal and diseased hearts. Springer US 2019-07-25 2019 /pmc/articles/PMC6785575/ /pubmed/31346662 http://dx.doi.org/10.1007/s00246-019-02160-w Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Riley Symposium
Jimenez, Jesus
Rentschler, Stacey L.
Transcriptional and Epigenetic Regulation of Cardiac Electrophysiology
title Transcriptional and Epigenetic Regulation of Cardiac Electrophysiology
title_full Transcriptional and Epigenetic Regulation of Cardiac Electrophysiology
title_fullStr Transcriptional and Epigenetic Regulation of Cardiac Electrophysiology
title_full_unstemmed Transcriptional and Epigenetic Regulation of Cardiac Electrophysiology
title_short Transcriptional and Epigenetic Regulation of Cardiac Electrophysiology
title_sort transcriptional and epigenetic regulation of cardiac electrophysiology
topic Riley Symposium
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6785575/
https://www.ncbi.nlm.nih.gov/pubmed/31346662
http://dx.doi.org/10.1007/s00246-019-02160-w
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