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Adaptive responses of histone modifications to resistance exercise in human skeletal muscle

Exercise training causes epigenetic changes in skeletal muscle, although it is unclear how resistance exercise (RE) affects histone modifications. The present study was carried out to investigate the effects of acute RE and RE training on gene expression profiles and histone modifications in human s...

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Autores principales: Lim, Changhyun, Shimizu, Junya, Kawano, Fuminori, Kim, Hyo Jeong, Kim, Chang Keun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145008/
https://www.ncbi.nlm.nih.gov/pubmed/32271843
http://dx.doi.org/10.1371/journal.pone.0231321
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author Lim, Changhyun
Shimizu, Junya
Kawano, Fuminori
Kim, Hyo Jeong
Kim, Chang Keun
author_facet Lim, Changhyun
Shimizu, Junya
Kawano, Fuminori
Kim, Hyo Jeong
Kim, Chang Keun
author_sort Lim, Changhyun
collection PubMed
description Exercise training causes epigenetic changes in skeletal muscle, although it is unclear how resistance exercise (RE) affects histone modifications. The present study was carried out to investigate the effects of acute RE and RE training on gene expression profiles and histone modifications in human skeletal muscle. Healthy male adults were assigned to acute RE (n = 9, age = 20.5±4.3yr, BMI = 28.0±6.8kg/m(2)) or RE training (n = 21, age = 23.7±2.5yr, BMI = 24.2±2.7kg/m(2)) groups. Biopsy samples were obtained from the vastus lateralis muscle before and three hours after a single bout of acute RE, or 3-days after 10 weeks of RE training. RNA sequencing analysis revealed that 153 genes with GO terms including muscle development, stress response, metabolism, cell death, and transcription factor were significantly up-regulated (+291% vs. pre-acute RE) upon acute RE. Expressions of these genes were also greater (+9.6% vs. pre-RE training, p<0.05) in RE trained subjects. Significant up-regulation of acetylated histone 3 (H3) (+235%) and H3 mono-methylated at lysine 4 (+290%) and tri-methylated at lysine 27 (+849%), whereas down-regulation of H3.3 variant (−39%) distributions relative to total H3 were observed at transcriptionally activated loci after acute RE compared to pre-acute RE levels. Interestingly, the distribution of acetylated H3 was found to be up-regulated as compared to the level of total H3 after RE training (+40%, p<0.05). These results indicate that a single bout of RE drastically alters both gene expressions and histone modifications in human skeletal muscle. It is also suggested that enhanced histone acetylation is closely related to up-regulation of gene expressions after RE training.
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spelling pubmed-71450082020-04-14 Adaptive responses of histone modifications to resistance exercise in human skeletal muscle Lim, Changhyun Shimizu, Junya Kawano, Fuminori Kim, Hyo Jeong Kim, Chang Keun PLoS One Research Article Exercise training causes epigenetic changes in skeletal muscle, although it is unclear how resistance exercise (RE) affects histone modifications. The present study was carried out to investigate the effects of acute RE and RE training on gene expression profiles and histone modifications in human skeletal muscle. Healthy male adults were assigned to acute RE (n = 9, age = 20.5±4.3yr, BMI = 28.0±6.8kg/m(2)) or RE training (n = 21, age = 23.7±2.5yr, BMI = 24.2±2.7kg/m(2)) groups. Biopsy samples were obtained from the vastus lateralis muscle before and three hours after a single bout of acute RE, or 3-days after 10 weeks of RE training. RNA sequencing analysis revealed that 153 genes with GO terms including muscle development, stress response, metabolism, cell death, and transcription factor were significantly up-regulated (+291% vs. pre-acute RE) upon acute RE. Expressions of these genes were also greater (+9.6% vs. pre-RE training, p<0.05) in RE trained subjects. Significant up-regulation of acetylated histone 3 (H3) (+235%) and H3 mono-methylated at lysine 4 (+290%) and tri-methylated at lysine 27 (+849%), whereas down-regulation of H3.3 variant (−39%) distributions relative to total H3 were observed at transcriptionally activated loci after acute RE compared to pre-acute RE levels. Interestingly, the distribution of acetylated H3 was found to be up-regulated as compared to the level of total H3 after RE training (+40%, p<0.05). These results indicate that a single bout of RE drastically alters both gene expressions and histone modifications in human skeletal muscle. It is also suggested that enhanced histone acetylation is closely related to up-regulation of gene expressions after RE training. Public Library of Science 2020-04-09 /pmc/articles/PMC7145008/ /pubmed/32271843 http://dx.doi.org/10.1371/journal.pone.0231321 Text en © 2020 Lim 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lim, Changhyun
Shimizu, Junya
Kawano, Fuminori
Kim, Hyo Jeong
Kim, Chang Keun
Adaptive responses of histone modifications to resistance exercise in human skeletal muscle
title Adaptive responses of histone modifications to resistance exercise in human skeletal muscle
title_full Adaptive responses of histone modifications to resistance exercise in human skeletal muscle
title_fullStr Adaptive responses of histone modifications to resistance exercise in human skeletal muscle
title_full_unstemmed Adaptive responses of histone modifications to resistance exercise in human skeletal muscle
title_short Adaptive responses of histone modifications to resistance exercise in human skeletal muscle
title_sort adaptive responses of histone modifications to resistance exercise in human skeletal muscle
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145008/
https://www.ncbi.nlm.nih.gov/pubmed/32271843
http://dx.doi.org/10.1371/journal.pone.0231321
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