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Heat stress and immune response phenotype affect DNA methylation in blood mononuclear cells from Holstein dairy cows
Heat stress negatively affects health and production in cows. Examining the cellular response to heat stress could reveal underlying protective molecular mechanisms associated with superior resilience and ultimately enable selection for more resilient cattle. This type of investigation is increasing...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166884/ https://www.ncbi.nlm.nih.gov/pubmed/34059695 http://dx.doi.org/10.1038/s41598-021-89951-5 |
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author | Livernois, A. M. Mallard, B. A. Cartwright, S. L. Cánovas, A. |
author_facet | Livernois, A. M. Mallard, B. A. Cartwright, S. L. Cánovas, A. |
author_sort | Livernois, A. M. |
collection | PubMed |
description | Heat stress negatively affects health and production in cows. Examining the cellular response to heat stress could reveal underlying protective molecular mechanisms associated with superior resilience and ultimately enable selection for more resilient cattle. This type of investigation is increasingly important as future predictions for the patterns of heat waves point to increases in frequency, severity, and duration. Cows identified as high immune responders based on High Immune Response technology (HIR) have lower disease occurrence compared to their average and low immune responder herd-mates. In this study, our goal was to identify epigenetic differences between high and low immune responder cows in response to heat stress. We examined genome-wide DNA methylation of blood mononuclear cells (BMCs) isolated from high and low cows, before and after in vitro heat stress. We identified differential methylation of promoter regions associated with a variety of biological processes including immune function, stress response, apoptosis, and cell signalling. The specific differentially methylated promoter regions differed between samples from high and low cows, and results revealed pathways associated with cellular protection during heat stress. |
format | Online Article Text |
id | pubmed-8166884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81668842021-06-01 Heat stress and immune response phenotype affect DNA methylation in blood mononuclear cells from Holstein dairy cows Livernois, A. M. Mallard, B. A. Cartwright, S. L. Cánovas, A. Sci Rep Article Heat stress negatively affects health and production in cows. Examining the cellular response to heat stress could reveal underlying protective molecular mechanisms associated with superior resilience and ultimately enable selection for more resilient cattle. This type of investigation is increasingly important as future predictions for the patterns of heat waves point to increases in frequency, severity, and duration. Cows identified as high immune responders based on High Immune Response technology (HIR) have lower disease occurrence compared to their average and low immune responder herd-mates. In this study, our goal was to identify epigenetic differences between high and low immune responder cows in response to heat stress. We examined genome-wide DNA methylation of blood mononuclear cells (BMCs) isolated from high and low cows, before and after in vitro heat stress. We identified differential methylation of promoter regions associated with a variety of biological processes including immune function, stress response, apoptosis, and cell signalling. The specific differentially methylated promoter regions differed between samples from high and low cows, and results revealed pathways associated with cellular protection during heat stress. Nature Publishing Group UK 2021-05-31 /pmc/articles/PMC8166884/ /pubmed/34059695 http://dx.doi.org/10.1038/s41598-021-89951-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Livernois, A. M. Mallard, B. A. Cartwright, S. L. Cánovas, A. Heat stress and immune response phenotype affect DNA methylation in blood mononuclear cells from Holstein dairy cows |
title | Heat stress and immune response phenotype affect DNA methylation in blood mononuclear cells from Holstein dairy cows |
title_full | Heat stress and immune response phenotype affect DNA methylation in blood mononuclear cells from Holstein dairy cows |
title_fullStr | Heat stress and immune response phenotype affect DNA methylation in blood mononuclear cells from Holstein dairy cows |
title_full_unstemmed | Heat stress and immune response phenotype affect DNA methylation in blood mononuclear cells from Holstein dairy cows |
title_short | Heat stress and immune response phenotype affect DNA methylation in blood mononuclear cells from Holstein dairy cows |
title_sort | heat stress and immune response phenotype affect dna methylation in blood mononuclear cells from holstein dairy cows |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166884/ https://www.ncbi.nlm.nih.gov/pubmed/34059695 http://dx.doi.org/10.1038/s41598-021-89951-5 |
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