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Genome-wide epigenetic dynamics during postnatal skeletal muscle growth in Hu sheep

Hypertrophy and fiber transformation are two prominent features of postnatal skeletal muscle development. However, the role of epigenetic modifications is less understood. ATAC-seq, whole genome bisulfite sequencing, and RNA-seq were applied to investigate the epigenetic dynamics of muscle in Hu she...

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Autores principales: Cao, Yutao, Ai, Yue, Zhang, Xiaosheng, Zhang, Jinlong, Long, Xianlei, Zhu, Yaning, Wang, Linli, Gu, Qingyi, Han, Hongbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593826/
https://www.ncbi.nlm.nih.gov/pubmed/37872364
http://dx.doi.org/10.1038/s42003-023-05439-0
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author Cao, Yutao
Ai, Yue
Zhang, Xiaosheng
Zhang, Jinlong
Long, Xianlei
Zhu, Yaning
Wang, Linli
Gu, Qingyi
Han, Hongbing
author_facet Cao, Yutao
Ai, Yue
Zhang, Xiaosheng
Zhang, Jinlong
Long, Xianlei
Zhu, Yaning
Wang, Linli
Gu, Qingyi
Han, Hongbing
author_sort Cao, Yutao
collection PubMed
description Hypertrophy and fiber transformation are two prominent features of postnatal skeletal muscle development. However, the role of epigenetic modifications is less understood. ATAC-seq, whole genome bisulfite sequencing, and RNA-seq were applied to investigate the epigenetic dynamics of muscle in Hu sheep at 3 days, 3 months, 6 months, and 12 months after birth. All 6865 differentially expressed genes were assigned into three distinct tendencies, highlighting the balanced protein synthesis, accumulated immune activities, and restrained cell division in postnatal development. We identified 3742 differentially accessible regions and 11799 differentially methylated regions that were associated with muscle-development-related pathways in certain stages, like D3-M6. Transcription factor network analysis, based on genomic loci with high chromatin accessibility and low methylation, showed that ARID5B, MYOG, and ENO1 were associated with muscle hypertrophy, while NR1D1, FADS1, ZFP36L2, and SLC25A1 were associated with muscle fiber transformation. Taken together, these results suggest that DNA methylation and chromatin accessibility contributed toward regulating the growth and fiber transformation of postnatal skeletal muscle in Hu sheep.
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spelling pubmed-105938262023-10-25 Genome-wide epigenetic dynamics during postnatal skeletal muscle growth in Hu sheep Cao, Yutao Ai, Yue Zhang, Xiaosheng Zhang, Jinlong Long, Xianlei Zhu, Yaning Wang, Linli Gu, Qingyi Han, Hongbing Commun Biol Article Hypertrophy and fiber transformation are two prominent features of postnatal skeletal muscle development. However, the role of epigenetic modifications is less understood. ATAC-seq, whole genome bisulfite sequencing, and RNA-seq were applied to investigate the epigenetic dynamics of muscle in Hu sheep at 3 days, 3 months, 6 months, and 12 months after birth. All 6865 differentially expressed genes were assigned into three distinct tendencies, highlighting the balanced protein synthesis, accumulated immune activities, and restrained cell division in postnatal development. We identified 3742 differentially accessible regions and 11799 differentially methylated regions that were associated with muscle-development-related pathways in certain stages, like D3-M6. Transcription factor network analysis, based on genomic loci with high chromatin accessibility and low methylation, showed that ARID5B, MYOG, and ENO1 were associated with muscle hypertrophy, while NR1D1, FADS1, ZFP36L2, and SLC25A1 were associated with muscle fiber transformation. Taken together, these results suggest that DNA methylation and chromatin accessibility contributed toward regulating the growth and fiber transformation of postnatal skeletal muscle in Hu sheep. Nature Publishing Group UK 2023-10-23 /pmc/articles/PMC10593826/ /pubmed/37872364 http://dx.doi.org/10.1038/s42003-023-05439-0 Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Cao, Yutao
Ai, Yue
Zhang, Xiaosheng
Zhang, Jinlong
Long, Xianlei
Zhu, Yaning
Wang, Linli
Gu, Qingyi
Han, Hongbing
Genome-wide epigenetic dynamics during postnatal skeletal muscle growth in Hu sheep
title Genome-wide epigenetic dynamics during postnatal skeletal muscle growth in Hu sheep
title_full Genome-wide epigenetic dynamics during postnatal skeletal muscle growth in Hu sheep
title_fullStr Genome-wide epigenetic dynamics during postnatal skeletal muscle growth in Hu sheep
title_full_unstemmed Genome-wide epigenetic dynamics during postnatal skeletal muscle growth in Hu sheep
title_short Genome-wide epigenetic dynamics during postnatal skeletal muscle growth in Hu sheep
title_sort genome-wide epigenetic dynamics during postnatal skeletal muscle growth in hu sheep
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593826/
https://www.ncbi.nlm.nih.gov/pubmed/37872364
http://dx.doi.org/10.1038/s42003-023-05439-0
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