Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Biga, Peggy R., Latimer, Mary N., Froehlich, Jacob Michael, Gabillard, Jean-Charles, Seiliez, Iban
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2017
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
_version_ 1783281717221523456
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
work_keys_str_mv AT bigapeggyr distributionofh3k27me3h3k9me3andh3k4me3alongautophagyrelatedgeneshighlyexpressedinstarvedzebrafishmyotubes
AT latimermaryn distributionofh3k27me3h3k9me3andh3k4me3alongautophagyrelatedgeneshighlyexpressedinstarvedzebrafishmyotubes
AT froehlichjacobmichael distributionofh3k27me3h3k9me3andh3k4me3alongautophagyrelatedgeneshighlyexpressedinstarvedzebrafishmyotubes
AT gabillardjeancharles distributionofh3k27me3h3k9me3andh3k4me3alongautophagyrelatedgeneshighlyexpressedinstarvedzebrafishmyotubes
AT seilieziban distributionofh3k27me3h3k9me3andh3k4me3alongautophagyrelatedgeneshighlyexpressedinstarvedzebrafishmyotubes