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Genome-Wide H3K4me3 Analysis in Angus Cattle with Divergent Tenderness
Tenderness is one of the most important properties of meat quality, which is influenced by genetic and environmental factors. As an intensively studied epigenetic marker, histone methylation, occurring on arginine and lysine residues, has pivotal regulatory functions on gene expression. To examine w...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4473007/ https://www.ncbi.nlm.nih.gov/pubmed/26086782 http://dx.doi.org/10.1371/journal.pone.0115358 |
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author | Zhao, Chunping Carrillo, José A. Tian, Fei Zan, Linsen Updike, Scott M. Zhao, Keji Zhan, Fei Song, Jiuzhou |
author_facet | Zhao, Chunping Carrillo, José A. Tian, Fei Zan, Linsen Updike, Scott M. Zhao, Keji Zhan, Fei Song, Jiuzhou |
author_sort | Zhao, Chunping |
collection | PubMed |
description | Tenderness is one of the most important properties of meat quality, which is influenced by genetic and environmental factors. As an intensively studied epigenetic marker, histone methylation, occurring on arginine and lysine residues, has pivotal regulatory functions on gene expression. To examine whether histone methylation involves in beef tenderness variation, we analyzed the transcriptome and H3K4me3 enrichment profiles of muscle strips obtained from the longissimus dorsi (LD) of Angus steers previously classify to the tender or tough group. We first plotted a global bovine H3K4me3 map on chromosomes and called peak-enriched regions and genes. We found that majorities of H3K4me3 on genes were occupying the first intron and intergenic regions and its maps displayed similar patterns in tender and tough groups, with high H3K4me3 enrichment surrounding the transcription start site (TSS). We also explored the relationship of H3K4me3 and gene expression. The results showed that H3K4me3 enrichment is highly positively correlated with gene expression across the whole genome. Cluster analysis results confirmed the relationship of H3K4me3 enrichment and gene expression. By using a pathway-based approach in genes with H3K4me3 enrichment in promoter regions from the tender cluster, we revealed that those genes involved in the development of different tissues–connective tissue, skeletal and muscular system and functional tissues–; while in tough group those genes engaged in cell death, lipid metabolism and small molecule biochemistry. The results from this study provide a deep insight into understanding of the mechanisms of epigenetic regulations in meat quality and beef tenderness. |
format | Online Article Text |
id | pubmed-4473007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44730072015-06-29 Genome-Wide H3K4me3 Analysis in Angus Cattle with Divergent Tenderness Zhao, Chunping Carrillo, José A. Tian, Fei Zan, Linsen Updike, Scott M. Zhao, Keji Zhan, Fei Song, Jiuzhou PLoS One Research Article Tenderness is one of the most important properties of meat quality, which is influenced by genetic and environmental factors. As an intensively studied epigenetic marker, histone methylation, occurring on arginine and lysine residues, has pivotal regulatory functions on gene expression. To examine whether histone methylation involves in beef tenderness variation, we analyzed the transcriptome and H3K4me3 enrichment profiles of muscle strips obtained from the longissimus dorsi (LD) of Angus steers previously classify to the tender or tough group. We first plotted a global bovine H3K4me3 map on chromosomes and called peak-enriched regions and genes. We found that majorities of H3K4me3 on genes were occupying the first intron and intergenic regions and its maps displayed similar patterns in tender and tough groups, with high H3K4me3 enrichment surrounding the transcription start site (TSS). We also explored the relationship of H3K4me3 and gene expression. The results showed that H3K4me3 enrichment is highly positively correlated with gene expression across the whole genome. Cluster analysis results confirmed the relationship of H3K4me3 enrichment and gene expression. By using a pathway-based approach in genes with H3K4me3 enrichment in promoter regions from the tender cluster, we revealed that those genes involved in the development of different tissues–connective tissue, skeletal and muscular system and functional tissues–; while in tough group those genes engaged in cell death, lipid metabolism and small molecule biochemistry. The results from this study provide a deep insight into understanding of the mechanisms of epigenetic regulations in meat quality and beef tenderness. Public Library of Science 2015-06-18 /pmc/articles/PMC4473007/ /pubmed/26086782 http://dx.doi.org/10.1371/journal.pone.0115358 Text en © 2015 Zhao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zhao, Chunping Carrillo, José A. Tian, Fei Zan, Linsen Updike, Scott M. Zhao, Keji Zhan, Fei Song, Jiuzhou Genome-Wide H3K4me3 Analysis in Angus Cattle with Divergent Tenderness |
title | Genome-Wide H3K4me3 Analysis in Angus Cattle with Divergent Tenderness |
title_full | Genome-Wide H3K4me3 Analysis in Angus Cattle with Divergent Tenderness |
title_fullStr | Genome-Wide H3K4me3 Analysis in Angus Cattle with Divergent Tenderness |
title_full_unstemmed | Genome-Wide H3K4me3 Analysis in Angus Cattle with Divergent Tenderness |
title_short | Genome-Wide H3K4me3 Analysis in Angus Cattle with Divergent Tenderness |
title_sort | genome-wide h3k4me3 analysis in angus cattle with divergent tenderness |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4473007/ https://www.ncbi.nlm.nih.gov/pubmed/26086782 http://dx.doi.org/10.1371/journal.pone.0115358 |
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