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Gene body methylation safeguards ribosomal DNA transcription by preventing PHF6-mediated enrichment of repressive histone mark H4K20me3
DNA methylation shows complex correlations with gene expression, and the role of promoter hypermethylation in repressing gene transcription has been well addressed. Emerging evidence indicates that gene body methylation promotes transcription; however, the underlying mechanisms remain to be further...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511956/ https://www.ncbi.nlm.nih.gov/pubmed/34520760 http://dx.doi.org/10.1016/j.jbc.2021.101195 |
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author | Huang, Xiaoke Zhang, Xuebin Zong, Le Gao, Qianqian Zhang, Chao Wei, Ran Guan, Yiting Huang, Li Zhang, Lijun Lyu, Guoliang Tao, Wei |
author_facet | Huang, Xiaoke Zhang, Xuebin Zong, Le Gao, Qianqian Zhang, Chao Wei, Ran Guan, Yiting Huang, Li Zhang, Lijun Lyu, Guoliang Tao, Wei |
author_sort | Huang, Xiaoke |
collection | PubMed |
description | DNA methylation shows complex correlations with gene expression, and the role of promoter hypermethylation in repressing gene transcription has been well addressed. Emerging evidence indicates that gene body methylation promotes transcription; however, the underlying mechanisms remain to be further investigated. Here, using methylated DNA immunoprecipitation sequencing (MeDIP-seq), bisulfite genomic sequencing, and immunofluorescent labeling, we show that gene body methylation is indeed positively correlated with rRNA gene (rDNA) transcription. Mechanistically, gene body methylation is largely maintained by DNA methyltransferase 1 (DNMT1), deficiency or downregulation of which during myoblast differentiation or nutrient deprivation results in decreased gene body methylation levels, leading to increased gene body occupancy of plant homeodomain (PHD) finger protein 6 (PHF6). PHF6 binds to hypomethylated rDNA gene bodies where it recruits histone methyltransferase SUV4-20H2 to establish the repressive histone modification, H4K20me3, ultimately inhibiting rDNA transcription. These findings demonstrate that DNMT1-mediated gene body methylation safeguards rDNA transcription by preventing enrichment of repressive histone modifications, suggesting that gene body methylation serves to maintain gene expression in response to developmental and/or environmental stresses. |
format | Online Article Text |
id | pubmed-8511956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-85119562021-10-21 Gene body methylation safeguards ribosomal DNA transcription by preventing PHF6-mediated enrichment of repressive histone mark H4K20me3 Huang, Xiaoke Zhang, Xuebin Zong, Le Gao, Qianqian Zhang, Chao Wei, Ran Guan, Yiting Huang, Li Zhang, Lijun Lyu, Guoliang Tao, Wei J Biol Chem Research Article DNA methylation shows complex correlations with gene expression, and the role of promoter hypermethylation in repressing gene transcription has been well addressed. Emerging evidence indicates that gene body methylation promotes transcription; however, the underlying mechanisms remain to be further investigated. Here, using methylated DNA immunoprecipitation sequencing (MeDIP-seq), bisulfite genomic sequencing, and immunofluorescent labeling, we show that gene body methylation is indeed positively correlated with rRNA gene (rDNA) transcription. Mechanistically, gene body methylation is largely maintained by DNA methyltransferase 1 (DNMT1), deficiency or downregulation of which during myoblast differentiation or nutrient deprivation results in decreased gene body methylation levels, leading to increased gene body occupancy of plant homeodomain (PHD) finger protein 6 (PHF6). PHF6 binds to hypomethylated rDNA gene bodies where it recruits histone methyltransferase SUV4-20H2 to establish the repressive histone modification, H4K20me3, ultimately inhibiting rDNA transcription. These findings demonstrate that DNMT1-mediated gene body methylation safeguards rDNA transcription by preventing enrichment of repressive histone modifications, suggesting that gene body methylation serves to maintain gene expression in response to developmental and/or environmental stresses. American Society for Biochemistry and Molecular Biology 2021-09-11 /pmc/articles/PMC8511956/ /pubmed/34520760 http://dx.doi.org/10.1016/j.jbc.2021.101195 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Huang, Xiaoke Zhang, Xuebin Zong, Le Gao, Qianqian Zhang, Chao Wei, Ran Guan, Yiting Huang, Li Zhang, Lijun Lyu, Guoliang Tao, Wei Gene body methylation safeguards ribosomal DNA transcription by preventing PHF6-mediated enrichment of repressive histone mark H4K20me3 |
title | Gene body methylation safeguards ribosomal DNA transcription by preventing PHF6-mediated enrichment of repressive histone mark H4K20me3 |
title_full | Gene body methylation safeguards ribosomal DNA transcription by preventing PHF6-mediated enrichment of repressive histone mark H4K20me3 |
title_fullStr | Gene body methylation safeguards ribosomal DNA transcription by preventing PHF6-mediated enrichment of repressive histone mark H4K20me3 |
title_full_unstemmed | Gene body methylation safeguards ribosomal DNA transcription by preventing PHF6-mediated enrichment of repressive histone mark H4K20me3 |
title_short | Gene body methylation safeguards ribosomal DNA transcription by preventing PHF6-mediated enrichment of repressive histone mark H4K20me3 |
title_sort | gene body methylation safeguards ribosomal dna transcription by preventing phf6-mediated enrichment of repressive histone mark h4k20me3 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511956/ https://www.ncbi.nlm.nih.gov/pubmed/34520760 http://dx.doi.org/10.1016/j.jbc.2021.101195 |
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