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Comparing DNA methylation profiles in saliva and intestinal mucosa
BACKGROUND: Altered epigenetic profiles are a feature of intestinal diseases, including ulcerative colitis and Crohn’s disease. DNA methylation studies in these diseases have utilised intestinal mucosal tissue or blood which can be difficult to collect, particularly for large-scale research studies....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394071/ https://www.ncbi.nlm.nih.gov/pubmed/30819108 http://dx.doi.org/10.1186/s12864-019-5553-0 |
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author | Hearn, Nerissa L. Coleman, Aaron S. Ho, Vincent Chiu, Christine L. Lind, Joanne M. |
author_facet | Hearn, Nerissa L. Coleman, Aaron S. Ho, Vincent Chiu, Christine L. Lind, Joanne M. |
author_sort | Hearn, Nerissa L. |
collection | PubMed |
description | BACKGROUND: Altered epigenetic profiles are a feature of intestinal diseases, including ulcerative colitis and Crohn’s disease. DNA methylation studies in these diseases have utilised intestinal mucosal tissue or blood which can be difficult to collect, particularly for large-scale research studies. Saliva is an attractive alternative for epigenetic studies as it is easy to collect and provides high quality methylation profiles. The aim of the study was to determine the utility of saliva as an alternative for DNA methylation studies of intestinal disorders. RESULTS: DNA methylation in saliva and intestinal mucosa samples were compared in individuals (n = 10) undergoing endoscopies using the Illumina Infinium Methylation 450 K Beadchip array. We found that DNA methylation was correlated between tissue types within an individual (Pearson correlation co-efficient r = 0.92 to 0.95, p < 0.001). Of the 48,541 probes (approximately 11% of CpG sites) that were differentially methylated between saliva and intestinal mucosa (adjusted p < 0.001, |Δβ| ≥ 20%), these mapped to genes involved in tissue-specific pathways, including the apelin signalling and oxytocin pathways which are important in gastrointestinal cytoprotection and motility. CONCLUSIONS: This study suggests that saliva has the potential to be used as an alternate DNA source to invasive intestinal mucosa for DNA methylation research into intestinal conditions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5553-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6394071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63940712019-03-11 Comparing DNA methylation profiles in saliva and intestinal mucosa Hearn, Nerissa L. Coleman, Aaron S. Ho, Vincent Chiu, Christine L. Lind, Joanne M. BMC Genomics Research Article BACKGROUND: Altered epigenetic profiles are a feature of intestinal diseases, including ulcerative colitis and Crohn’s disease. DNA methylation studies in these diseases have utilised intestinal mucosal tissue or blood which can be difficult to collect, particularly for large-scale research studies. Saliva is an attractive alternative for epigenetic studies as it is easy to collect and provides high quality methylation profiles. The aim of the study was to determine the utility of saliva as an alternative for DNA methylation studies of intestinal disorders. RESULTS: DNA methylation in saliva and intestinal mucosa samples were compared in individuals (n = 10) undergoing endoscopies using the Illumina Infinium Methylation 450 K Beadchip array. We found that DNA methylation was correlated between tissue types within an individual (Pearson correlation co-efficient r = 0.92 to 0.95, p < 0.001). Of the 48,541 probes (approximately 11% of CpG sites) that were differentially methylated between saliva and intestinal mucosa (adjusted p < 0.001, |Δβ| ≥ 20%), these mapped to genes involved in tissue-specific pathways, including the apelin signalling and oxytocin pathways which are important in gastrointestinal cytoprotection and motility. CONCLUSIONS: This study suggests that saliva has the potential to be used as an alternate DNA source to invasive intestinal mucosa for DNA methylation research into intestinal conditions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5553-0) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-28 /pmc/articles/PMC6394071/ /pubmed/30819108 http://dx.doi.org/10.1186/s12864-019-5553-0 Text en © The Author(s). 2019 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 Hearn, Nerissa L. Coleman, Aaron S. Ho, Vincent Chiu, Christine L. Lind, Joanne M. Comparing DNA methylation profiles in saliva and intestinal mucosa |
title | Comparing DNA methylation profiles in saliva and intestinal mucosa |
title_full | Comparing DNA methylation profiles in saliva and intestinal mucosa |
title_fullStr | Comparing DNA methylation profiles in saliva and intestinal mucosa |
title_full_unstemmed | Comparing DNA methylation profiles in saliva and intestinal mucosa |
title_short | Comparing DNA methylation profiles in saliva and intestinal mucosa |
title_sort | comparing dna methylation profiles in saliva and intestinal mucosa |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394071/ https://www.ncbi.nlm.nih.gov/pubmed/30819108 http://dx.doi.org/10.1186/s12864-019-5553-0 |
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