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Heterogeneous pattern of DNA methylation in developmentally important genes correlates with its chromatin conformation
BACKGROUND: DNA methylation is a major epigenetic modification, playing a crucial role in the development and differentiation of higher organisms. DNA methylation is also known to regulate transcription by gene repression. Various developmental genes such as c-mos, HoxB5, Sox11, and Sry show tissue-...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5234095/ https://www.ncbi.nlm.nih.gov/pubmed/28081716 http://dx.doi.org/10.1186/s12867-016-0078-4 |
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author | Sinha, Puja Singh, Kiran Sachan, Manisha |
author_facet | Sinha, Puja Singh, Kiran Sachan, Manisha |
author_sort | Sinha, Puja |
collection | PubMed |
description | BACKGROUND: DNA methylation is a major epigenetic modification, playing a crucial role in the development and differentiation of higher organisms. DNA methylation is also known to regulate transcription by gene repression. Various developmental genes such as c-mos, HoxB5, Sox11, and Sry show tissue-specific gene expression that was shown to be regulated by promoter DNA methylation. The aim of the present study is to investigate the establishment of chromatin marks (active or repressive) in relation to heterogeneous methylation in the promoter regions of these developmentally important genes. RESULTS: Chromatin-immunoprecipitation (ChIP) assays were performed to immuno-precipitate chromatin by antibodies against both active (H3K4me3) and repressive (H3K9me3) chromatin regions. The analysis of ChIP results showed that both the percentage input and fold enrichment of activated chromatin was higher in tissues expressing the respective genes as compared to the tissues not expressing the same set of genes. This was true for all the genes selected for the study (c-mos, HoxB5, Sox11, and Sry). These findings illustrate that inconsistent DNA methylation patterns (sporadic, mosaic and heterogeneous) may also influence gene regulation, thereby resulting in the modulation of chromatin conformation. CONCLUSIONS: These findings illustrate that various patterns of DNA methylation (asynchronous, mosaic and heterogeneous) correlates with chromatin modification, resulting in the gene regulation. |
format | Online Article Text |
id | pubmed-5234095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52340952017-01-17 Heterogeneous pattern of DNA methylation in developmentally important genes correlates with its chromatin conformation Sinha, Puja Singh, Kiran Sachan, Manisha BMC Mol Biol Research Article BACKGROUND: DNA methylation is a major epigenetic modification, playing a crucial role in the development and differentiation of higher organisms. DNA methylation is also known to regulate transcription by gene repression. Various developmental genes such as c-mos, HoxB5, Sox11, and Sry show tissue-specific gene expression that was shown to be regulated by promoter DNA methylation. The aim of the present study is to investigate the establishment of chromatin marks (active or repressive) in relation to heterogeneous methylation in the promoter regions of these developmentally important genes. RESULTS: Chromatin-immunoprecipitation (ChIP) assays were performed to immuno-precipitate chromatin by antibodies against both active (H3K4me3) and repressive (H3K9me3) chromatin regions. The analysis of ChIP results showed that both the percentage input and fold enrichment of activated chromatin was higher in tissues expressing the respective genes as compared to the tissues not expressing the same set of genes. This was true for all the genes selected for the study (c-mos, HoxB5, Sox11, and Sry). These findings illustrate that inconsistent DNA methylation patterns (sporadic, mosaic and heterogeneous) may also influence gene regulation, thereby resulting in the modulation of chromatin conformation. CONCLUSIONS: These findings illustrate that various patterns of DNA methylation (asynchronous, mosaic and heterogeneous) correlates with chromatin modification, resulting in the gene regulation. BioMed Central 2017-01-11 /pmc/articles/PMC5234095/ /pubmed/28081716 http://dx.doi.org/10.1186/s12867-016-0078-4 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Sinha, Puja Singh, Kiran Sachan, Manisha Heterogeneous pattern of DNA methylation in developmentally important genes correlates with its chromatin conformation |
title | Heterogeneous pattern of DNA methylation in developmentally important genes correlates with its chromatin conformation |
title_full | Heterogeneous pattern of DNA methylation in developmentally important genes correlates with its chromatin conformation |
title_fullStr | Heterogeneous pattern of DNA methylation in developmentally important genes correlates with its chromatin conformation |
title_full_unstemmed | Heterogeneous pattern of DNA methylation in developmentally important genes correlates with its chromatin conformation |
title_short | Heterogeneous pattern of DNA methylation in developmentally important genes correlates with its chromatin conformation |
title_sort | heterogeneous pattern of dna methylation in developmentally important genes correlates with its chromatin conformation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5234095/ https://www.ncbi.nlm.nih.gov/pubmed/28081716 http://dx.doi.org/10.1186/s12867-016-0078-4 |
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