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Distribution of H3K27me3, H3K9me3, and H3K4me3 along autophagy-related genes highly expressed in starved zebrafish myotubes
The zebrafish (Danio rerio) remains the teleost fish of choice for biological investigations due to the vast array of molecular tools and resources available. To better understand the epigenetic regulation of autophagy, we utilized a primary myotube culture system generated from isolated myogenic pr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703616/ https://www.ncbi.nlm.nih.gov/pubmed/29025701 http://dx.doi.org/10.1242/bio.029090 |
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author | Biga, Peggy R. Latimer, Mary N. Froehlich, Jacob Michael Gabillard, Jean-Charles Seiliez, Iban |
author_facet | Biga, Peggy R. Latimer, Mary N. Froehlich, Jacob Michael Gabillard, Jean-Charles Seiliez, Iban |
author_sort | Biga, Peggy R. |
collection | PubMed |
description | The zebrafish (Danio rerio) remains the teleost fish of choice for biological investigations due to the vast array of molecular tools and resources available. To better understand the epigenetic regulation of autophagy, we utilized a primary myotube culture system generated from isolated myogenic precursor cells (MPCs) from zebrafish grown under starvation conditions using a media devoid of serum and amino acids. Here, we report starvation-induced regulation of several autophagy-related genes (atg) expression and profile the distribution of H3K27me3, H3K9me3, and H3K4me3 marks along lc3b, atg4b and p62/sqstm1 loci. These data support epigenetic regulation of autophagy in response to starvation that suggests a level of regulation that can be sustained for chronic conditions via chromatin modification. |
format | Online Article Text |
id | pubmed-5703616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57036162017-12-06 Distribution of H3K27me3, H3K9me3, and H3K4me3 along autophagy-related genes highly expressed in starved zebrafish myotubes Biga, Peggy R. Latimer, Mary N. Froehlich, Jacob Michael Gabillard, Jean-Charles Seiliez, Iban Biol Open Research Article The zebrafish (Danio rerio) remains the teleost fish of choice for biological investigations due to the vast array of molecular tools and resources available. To better understand the epigenetic regulation of autophagy, we utilized a primary myotube culture system generated from isolated myogenic precursor cells (MPCs) from zebrafish grown under starvation conditions using a media devoid of serum and amino acids. Here, we report starvation-induced regulation of several autophagy-related genes (atg) expression and profile the distribution of H3K27me3, H3K9me3, and H3K4me3 marks along lc3b, atg4b and p62/sqstm1 loci. These data support epigenetic regulation of autophagy in response to starvation that suggests a level of regulation that can be sustained for chronic conditions via chromatin modification. The Company of Biologists Ltd 2017-10-12 /pmc/articles/PMC5703616/ /pubmed/29025701 http://dx.doi.org/10.1242/bio.029090 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Biga, Peggy R. Latimer, Mary N. Froehlich, Jacob Michael Gabillard, Jean-Charles Seiliez, Iban Distribution of H3K27me3, H3K9me3, and H3K4me3 along autophagy-related genes highly expressed in starved zebrafish myotubes |
title | Distribution of H3K27me3, H3K9me3, and H3K4me3 along autophagy-related genes highly expressed in starved zebrafish myotubes |
title_full | Distribution of H3K27me3, H3K9me3, and H3K4me3 along autophagy-related genes highly expressed in starved zebrafish myotubes |
title_fullStr | Distribution of H3K27me3, H3K9me3, and H3K4me3 along autophagy-related genes highly expressed in starved zebrafish myotubes |
title_full_unstemmed | Distribution of H3K27me3, H3K9me3, and H3K4me3 along autophagy-related genes highly expressed in starved zebrafish myotubes |
title_short | Distribution of H3K27me3, H3K9me3, and H3K4me3 along autophagy-related genes highly expressed in starved zebrafish myotubes |
title_sort | distribution of h3k27me3, h3k9me3, and h3k4me3 along autophagy-related genes highly expressed in starved zebrafish myotubes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703616/ https://www.ncbi.nlm.nih.gov/pubmed/29025701 http://dx.doi.org/10.1242/bio.029090 |
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