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H3K36 Methylation in Neural Development and Associated Diseases
Post-translational methylation of H3 lysine 36 (H3K36) is an important epigenetic marker that majorly contributes to the functionality of the chromatin. This mark is interpreted by the cell in several crucial biological processes including gene transcription and DNA methylation. The homeostasis of H...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962298/ https://www.ncbi.nlm.nih.gov/pubmed/31998360 http://dx.doi.org/10.3389/fgene.2019.01291 |
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author | Zaghi, Mattia Broccoli, Vania Sessa, Alessandro |
author_facet | Zaghi, Mattia Broccoli, Vania Sessa, Alessandro |
author_sort | Zaghi, Mattia |
collection | PubMed |
description | Post-translational methylation of H3 lysine 36 (H3K36) is an important epigenetic marker that majorly contributes to the functionality of the chromatin. This mark is interpreted by the cell in several crucial biological processes including gene transcription and DNA methylation. The homeostasis of H3K36 methylation is finely regulated by different enzyme classes which, when impaired, lead to a plethora of diseases; ranging from multi-organ syndromes to cancer, to pure neurological diseases often associated with brain development. This mini-review summarizes current knowledge on these important epigenetic signals with emphasis on the molecular mechanisms that (i) regulate their abundance, (ii) are influenced by H3K36 methylation, and (iii) the associated diseases. |
format | Online Article Text |
id | pubmed-6962298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69622982020-01-29 H3K36 Methylation in Neural Development and Associated Diseases Zaghi, Mattia Broccoli, Vania Sessa, Alessandro Front Genet Genetics Post-translational methylation of H3 lysine 36 (H3K36) is an important epigenetic marker that majorly contributes to the functionality of the chromatin. This mark is interpreted by the cell in several crucial biological processes including gene transcription and DNA methylation. The homeostasis of H3K36 methylation is finely regulated by different enzyme classes which, when impaired, lead to a plethora of diseases; ranging from multi-organ syndromes to cancer, to pure neurological diseases often associated with brain development. This mini-review summarizes current knowledge on these important epigenetic signals with emphasis on the molecular mechanisms that (i) regulate their abundance, (ii) are influenced by H3K36 methylation, and (iii) the associated diseases. Frontiers Media S.A. 2020-01-09 /pmc/articles/PMC6962298/ /pubmed/31998360 http://dx.doi.org/10.3389/fgene.2019.01291 Text en Copyright © 2020 Zaghi, Broccoli and Sessa http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Zaghi, Mattia Broccoli, Vania Sessa, Alessandro H3K36 Methylation in Neural Development and Associated Diseases |
title | H3K36 Methylation in Neural Development and Associated Diseases |
title_full | H3K36 Methylation in Neural Development and Associated Diseases |
title_fullStr | H3K36 Methylation in Neural Development and Associated Diseases |
title_full_unstemmed | H3K36 Methylation in Neural Development and Associated Diseases |
title_short | H3K36 Methylation in Neural Development and Associated Diseases |
title_sort | h3k36 methylation in neural development and associated diseases |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962298/ https://www.ncbi.nlm.nih.gov/pubmed/31998360 http://dx.doi.org/10.3389/fgene.2019.01291 |
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