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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...

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Autores principales: Zhao, Chunping, Carrillo, José A., Tian, Fei, Zan, Linsen, Updike, Scott M., Zhao, Keji, Zhan, Fei, Song, Jiuzhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
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.
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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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