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Characterization of H3K9me3 and DNA methylation co-marked CpG-rich regions during mouse development

BACKGROUND: H3K9me3 and DNA methylation co-marked CpG-rich regions (CHMs) are functionally important in mouse pre-implantation embryos, but their characteristics in other biological processes are still largely unknown. RESULTS: In this study, we performed a comprehensive analysis to characterize CHM...

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Autores principales: Yang, Hui, Wang, Yiman, Zhang, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623782/
https://www.ncbi.nlm.nih.gov/pubmed/37924034
http://dx.doi.org/10.1186/s12864-023-09758-8
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author Yang, Hui
Wang, Yiman
Zhang, Yong
author_facet Yang, Hui
Wang, Yiman
Zhang, Yong
author_sort Yang, Hui
collection PubMed
description BACKGROUND: H3K9me3 and DNA methylation co-marked CpG-rich regions (CHMs) are functionally important in mouse pre-implantation embryos, but their characteristics in other biological processes are still largely unknown. RESULTS: In this study, we performed a comprehensive analysis to characterize CHMs during 6 mouse developmental processes, identifying over 2,600 CHMs exhibiting stable co-mark of H3K9me3 and DNA methylation patterns at CpG-rich regions. We revealed the distinctive features of CHMs, including elevated H3K9me3 signals and a significant presence in euchromatin and the potential role in silencing younger long terminal repeats (LTRs), especially in some ERVK subfamilies. The results highlight the distinct nature of universal CHMs compared to CpG-rich nonCHMs in terms of location, LTR enrichment, and DNA sequence features, enhancing our understanding of CpG-rich regions' regulatory roles. CONCLUSIONS: This study characterizes the features of CHMs in multiple developmental processes and broadens our understanding of the regulatory roles of CpG-rich regions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09758-8.
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spelling pubmed-106237822023-11-04 Characterization of H3K9me3 and DNA methylation co-marked CpG-rich regions during mouse development Yang, Hui Wang, Yiman Zhang, Yong BMC Genomics Research BACKGROUND: H3K9me3 and DNA methylation co-marked CpG-rich regions (CHMs) are functionally important in mouse pre-implantation embryos, but their characteristics in other biological processes are still largely unknown. RESULTS: In this study, we performed a comprehensive analysis to characterize CHMs during 6 mouse developmental processes, identifying over 2,600 CHMs exhibiting stable co-mark of H3K9me3 and DNA methylation patterns at CpG-rich regions. We revealed the distinctive features of CHMs, including elevated H3K9me3 signals and a significant presence in euchromatin and the potential role in silencing younger long terminal repeats (LTRs), especially in some ERVK subfamilies. The results highlight the distinct nature of universal CHMs compared to CpG-rich nonCHMs in terms of location, LTR enrichment, and DNA sequence features, enhancing our understanding of CpG-rich regions' regulatory roles. CONCLUSIONS: This study characterizes the features of CHMs in multiple developmental processes and broadens our understanding of the regulatory roles of CpG-rich regions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09758-8. BioMed Central 2023-11-03 /pmc/articles/PMC10623782/ /pubmed/37924034 http://dx.doi.org/10.1186/s12864-023-09758-8 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 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yang, Hui
Wang, Yiman
Zhang, Yong
Characterization of H3K9me3 and DNA methylation co-marked CpG-rich regions during mouse development
title Characterization of H3K9me3 and DNA methylation co-marked CpG-rich regions during mouse development
title_full Characterization of H3K9me3 and DNA methylation co-marked CpG-rich regions during mouse development
title_fullStr Characterization of H3K9me3 and DNA methylation co-marked CpG-rich regions during mouse development
title_full_unstemmed Characterization of H3K9me3 and DNA methylation co-marked CpG-rich regions during mouse development
title_short Characterization of H3K9me3 and DNA methylation co-marked CpG-rich regions during mouse development
title_sort characterization of h3k9me3 and dna methylation co-marked cpg-rich regions during mouse development
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623782/
https://www.ncbi.nlm.nih.gov/pubmed/37924034
http://dx.doi.org/10.1186/s12864-023-09758-8
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