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The Profiling of DNA Methylation and Its Regulation on Divergent Tenderness in Angus Beef Cattle

Beef is an essential food source in the world. Beef quality, especially tenderness, has a significant impact on consumer satisfaction and industry profit. Many types of research to date have focused on the exploration of physiological and developmental mechanisms of beef tenderness. Still, the role...

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Autores principales: Zhao, Chunping, Ji, Guanyu, Carrillo, José A., Li, Yaokun, Tian, Fei, Baldwin, Ransom L., Zan, Linsen, Song, Jiuzhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7479246/
https://www.ncbi.nlm.nih.gov/pubmed/33005170
http://dx.doi.org/10.3389/fgene.2020.00939
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author Zhao, Chunping
Ji, Guanyu
Carrillo, José A.
Li, Yaokun
Tian, Fei
Baldwin, Ransom L.
Zan, Linsen
Song, Jiuzhou
author_facet Zhao, Chunping
Ji, Guanyu
Carrillo, José A.
Li, Yaokun
Tian, Fei
Baldwin, Ransom L.
Zan, Linsen
Song, Jiuzhou
author_sort Zhao, Chunping
collection PubMed
description Beef is an essential food source in the world. Beef quality, especially tenderness, has a significant impact on consumer satisfaction and industry profit. Many types of research to date have focused on the exploration of physiological and developmental mechanisms of beef tenderness. Still, the role and impact of DNA methylation status on beef tenderness have yet to be elucidated. In this study, we exhaustively analyzed the DNA methylation status in divergent tenderness observed in Angus beef. We characterized the methylation profiles related to beef tenderness and explored methylation distributions on the whole genome. As a result, differentially methylated regions (DMRs) associated with tenderness and toughness of beef were identified. Importantly, we annotated these DMRs on the bovine genome and explored bio-pathways of underlying genes and methylation biomarkers in beef quality. Specifically, we observed that the ATP binding cassette subfamily and myosin-related genes were highly methylated gene sets, and generation of neurons, regulation of GTPase activity, ion transport and anion transport, etc., were the significant pathways related with beef tenderness. Moreover, we explored the relationship between DNA methylation and gene expression in DMRs. Some methylated genes were identified as candidate biomarkers for beef tenderness. These results provide not only novel epigenetic information associated with beef quality but offer more significant insights into meat science, which will further help us explore the mechanism of muscle biology.
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spelling pubmed-74792462020-09-30 The Profiling of DNA Methylation and Its Regulation on Divergent Tenderness in Angus Beef Cattle Zhao, Chunping Ji, Guanyu Carrillo, José A. Li, Yaokun Tian, Fei Baldwin, Ransom L. Zan, Linsen Song, Jiuzhou Front Genet Genetics Beef is an essential food source in the world. Beef quality, especially tenderness, has a significant impact on consumer satisfaction and industry profit. Many types of research to date have focused on the exploration of physiological and developmental mechanisms of beef tenderness. Still, the role and impact of DNA methylation status on beef tenderness have yet to be elucidated. In this study, we exhaustively analyzed the DNA methylation status in divergent tenderness observed in Angus beef. We characterized the methylation profiles related to beef tenderness and explored methylation distributions on the whole genome. As a result, differentially methylated regions (DMRs) associated with tenderness and toughness of beef were identified. Importantly, we annotated these DMRs on the bovine genome and explored bio-pathways of underlying genes and methylation biomarkers in beef quality. Specifically, we observed that the ATP binding cassette subfamily and myosin-related genes were highly methylated gene sets, and generation of neurons, regulation of GTPase activity, ion transport and anion transport, etc., were the significant pathways related with beef tenderness. Moreover, we explored the relationship between DNA methylation and gene expression in DMRs. Some methylated genes were identified as candidate biomarkers for beef tenderness. These results provide not only novel epigenetic information associated with beef quality but offer more significant insights into meat science, which will further help us explore the mechanism of muscle biology. Frontiers Media S.A. 2020-08-26 /pmc/articles/PMC7479246/ /pubmed/33005170 http://dx.doi.org/10.3389/fgene.2020.00939 Text en Copyright © 2020 Zhao, Ji, Carrillo, Li, Tian, Baldwin, Zan and Song. 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
Zhao, Chunping
Ji, Guanyu
Carrillo, José A.
Li, Yaokun
Tian, Fei
Baldwin, Ransom L.
Zan, Linsen
Song, Jiuzhou
The Profiling of DNA Methylation and Its Regulation on Divergent Tenderness in Angus Beef Cattle
title The Profiling of DNA Methylation and Its Regulation on Divergent Tenderness in Angus Beef Cattle
title_full The Profiling of DNA Methylation and Its Regulation on Divergent Tenderness in Angus Beef Cattle
title_fullStr The Profiling of DNA Methylation and Its Regulation on Divergent Tenderness in Angus Beef Cattle
title_full_unstemmed The Profiling of DNA Methylation and Its Regulation on Divergent Tenderness in Angus Beef Cattle
title_short The Profiling of DNA Methylation and Its Regulation on Divergent Tenderness in Angus Beef Cattle
title_sort profiling of dna methylation and its regulation on divergent tenderness in angus beef cattle
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7479246/
https://www.ncbi.nlm.nih.gov/pubmed/33005170
http://dx.doi.org/10.3389/fgene.2020.00939
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