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The Roles of Histone Lysine Methyltransferases in Heart Development and Disease

Epigenetic marks regulate the transcriptomic landscape by facilitating the structural packing and unwinding of the genome, which is tightly folded inside the nucleus. Lysine-specific histone methylation is one such mark. It plays crucial roles during development, including in cell fate decisions, in...

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Autores principales: Zhu, Jun-yi, van de Leemput, Joyce, Han, Zhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380575/
https://www.ncbi.nlm.nih.gov/pubmed/37504561
http://dx.doi.org/10.3390/jcdd10070305
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author Zhu, Jun-yi
van de Leemput, Joyce
Han, Zhe
author_facet Zhu, Jun-yi
van de Leemput, Joyce
Han, Zhe
author_sort Zhu, Jun-yi
collection PubMed
description Epigenetic marks regulate the transcriptomic landscape by facilitating the structural packing and unwinding of the genome, which is tightly folded inside the nucleus. Lysine-specific histone methylation is one such mark. It plays crucial roles during development, including in cell fate decisions, in tissue patterning, and in regulating cellular metabolic processes. It has also been associated with varying human developmental disorders. Heart disease has been linked to deregulated histone lysine methylation, and lysine-specific methyltransferases (KMTs) are overrepresented, i.e., more numerous than expected by chance, among the genes with variants associated with congenital heart disease. This review outlines the available evidence to support a role for individual KMTs in heart development and/or disease, including genetic associations in patients and supporting cell culture and animal model studies. It concludes with new advances in the field and new opportunities for treatment.
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spelling pubmed-103805752023-07-29 The Roles of Histone Lysine Methyltransferases in Heart Development and Disease Zhu, Jun-yi van de Leemput, Joyce Han, Zhe J Cardiovasc Dev Dis Review Epigenetic marks regulate the transcriptomic landscape by facilitating the structural packing and unwinding of the genome, which is tightly folded inside the nucleus. Lysine-specific histone methylation is one such mark. It plays crucial roles during development, including in cell fate decisions, in tissue patterning, and in regulating cellular metabolic processes. It has also been associated with varying human developmental disorders. Heart disease has been linked to deregulated histone lysine methylation, and lysine-specific methyltransferases (KMTs) are overrepresented, i.e., more numerous than expected by chance, among the genes with variants associated with congenital heart disease. This review outlines the available evidence to support a role for individual KMTs in heart development and/or disease, including genetic associations in patients and supporting cell culture and animal model studies. It concludes with new advances in the field and new opportunities for treatment. MDPI 2023-07-18 /pmc/articles/PMC10380575/ /pubmed/37504561 http://dx.doi.org/10.3390/jcdd10070305 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Zhu, Jun-yi
van de Leemput, Joyce
Han, Zhe
The Roles of Histone Lysine Methyltransferases in Heart Development and Disease
title The Roles of Histone Lysine Methyltransferases in Heart Development and Disease
title_full The Roles of Histone Lysine Methyltransferases in Heart Development and Disease
title_fullStr The Roles of Histone Lysine Methyltransferases in Heart Development and Disease
title_full_unstemmed The Roles of Histone Lysine Methyltransferases in Heart Development and Disease
title_short The Roles of Histone Lysine Methyltransferases in Heart Development and Disease
title_sort roles of histone lysine methyltransferases in heart development and disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380575/
https://www.ncbi.nlm.nih.gov/pubmed/37504561
http://dx.doi.org/10.3390/jcdd10070305
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