A cost-effective approach to DNA methylation detection by Methyl Sensitive DArT sequencing.

Several studies suggest the relation of DNA methylation to diseases in humans and important phenotypes in plants drawing attention to this epigenetic mark as an important source of variability. In the last decades, several methodologies were developed to assess the methylation state of a genome. How...

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Main Authors: Wendell Jacinto Pereira, Marília de Castro Rodrigues Pappas, Dario Grattapaglia, Georgios Joannis Pappas
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0233800
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spelling doaj-03cd71454631446693f8df8d5ba5a32b2021-03-03T21:50:24ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01156e023380010.1371/journal.pone.0233800A cost-effective approach to DNA methylation detection by Methyl Sensitive DArT sequencing.Wendell Jacinto PereiraMarília de Castro Rodrigues PappasDario GrattapagliaGeorgios Joannis PappasSeveral studies suggest the relation of DNA methylation to diseases in humans and important phenotypes in plants drawing attention to this epigenetic mark as an important source of variability. In the last decades, several methodologies were developed to assess the methylation state of a genome. However, there is still a lack of affordable and precise methods for genome wide analysis in large sample size studies. Methyl sensitive double digestion MS-DArT sequencing method emerges as a promising alternative for methylation profiling. We developed a computational pipeline for the identification of DNA methylation using MS-DArT-seq data and carried out a pilot study using the Eucalyptus grandis tree sequenced for the species reference genome. Using a statistic framework as in differential expression analysis, 72,515 genomic sites were investigated and 5,846 methylated sites identified, several tissue specific, distributed along the species 11 chromosomes. We highlight a bias towards identification of DNA methylation in genic regions and the identification of 2,783 genes and 842 transposons containing methylated sites. Comparison with WGBS, DNA sequencing after treatment with bisulfite, data demonstrated a precision rate higher than 95% for our approach. The availability of a reference genome is useful for determining the genomic context of methylated sites but not imperative, making this approach suitable for any species. Our approach provides a cost effective, broad and reliable examination of DNA methylation profile on MspI/HpaII restriction sites, is fully reproducible and the source code is available on GitHub (https://github.com/wendelljpereira/ms-dart-seq).https://doi.org/10.1371/journal.pone.0233800
collection DOAJ
language English
format Article
sources DOAJ
author Wendell Jacinto Pereira
Marília de Castro Rodrigues Pappas
Dario Grattapaglia
Georgios Joannis Pappas
spellingShingle Wendell Jacinto Pereira
Marília de Castro Rodrigues Pappas
Dario Grattapaglia
Georgios Joannis Pappas
A cost-effective approach to DNA methylation detection by Methyl Sensitive DArT sequencing.
PLoS ONE
author_facet Wendell Jacinto Pereira
Marília de Castro Rodrigues Pappas
Dario Grattapaglia
Georgios Joannis Pappas
author_sort Wendell Jacinto Pereira
title A cost-effective approach to DNA methylation detection by Methyl Sensitive DArT sequencing.
title_short A cost-effective approach to DNA methylation detection by Methyl Sensitive DArT sequencing.
title_full A cost-effective approach to DNA methylation detection by Methyl Sensitive DArT sequencing.
title_fullStr A cost-effective approach to DNA methylation detection by Methyl Sensitive DArT sequencing.
title_full_unstemmed A cost-effective approach to DNA methylation detection by Methyl Sensitive DArT sequencing.
title_sort cost-effective approach to dna methylation detection by methyl sensitive dart sequencing.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2020-01-01
description Several studies suggest the relation of DNA methylation to diseases in humans and important phenotypes in plants drawing attention to this epigenetic mark as an important source of variability. In the last decades, several methodologies were developed to assess the methylation state of a genome. However, there is still a lack of affordable and precise methods for genome wide analysis in large sample size studies. Methyl sensitive double digestion MS-DArT sequencing method emerges as a promising alternative for methylation profiling. We developed a computational pipeline for the identification of DNA methylation using MS-DArT-seq data and carried out a pilot study using the Eucalyptus grandis tree sequenced for the species reference genome. Using a statistic framework as in differential expression analysis, 72,515 genomic sites were investigated and 5,846 methylated sites identified, several tissue specific, distributed along the species 11 chromosomes. We highlight a bias towards identification of DNA methylation in genic regions and the identification of 2,783 genes and 842 transposons containing methylated sites. Comparison with WGBS, DNA sequencing after treatment with bisulfite, data demonstrated a precision rate higher than 95% for our approach. The availability of a reference genome is useful for determining the genomic context of methylated sites but not imperative, making this approach suitable for any species. Our approach provides a cost effective, broad and reliable examination of DNA methylation profile on MspI/HpaII restriction sites, is fully reproducible and the source code is available on GitHub (https://github.com/wendelljpereira/ms-dart-seq).
url https://doi.org/10.1371/journal.pone.0233800
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