Cargando…
Modeling DNA methylation dynamics with approaches from phylogenetics
Motivation: Methylation of CpG dinucleotides is a prevalent epigenetic modification that is required for proper development in vertebrates. Genome-wide DNA methylation assays have become increasingly common, and this has enabled characterization of DNA methylation in distinct stages across different...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147898/ https://www.ncbi.nlm.nih.gov/pubmed/25161227 http://dx.doi.org/10.1093/bioinformatics/btu445 |
_version_ | 1782332532804550656 |
---|---|
author | Capra, John A. Kostka, Dennis |
author_facet | Capra, John A. Kostka, Dennis |
author_sort | Capra, John A. |
collection | PubMed |
description | Motivation: Methylation of CpG dinucleotides is a prevalent epigenetic modification that is required for proper development in vertebrates. Genome-wide DNA methylation assays have become increasingly common, and this has enabled characterization of DNA methylation in distinct stages across differentiating cellular lineages. Changes in CpG methylation are essential to cellular differentiation; however, current methods for modeling methylation dynamics do not account for the dependency structure between precursor and dependent cell types. Results: We developed a continuous-time Markov chain approach, based on the observation that changes in methylation state over tissue differentiation can be modeled similarly to DNA nucleotide changes over evolutionary time. This model explicitly takes precursor to descendant relationships into account and enables inference of CpG methylation dynamics. To illustrate our method, we analyzed a high-resolution methylation map of the differentiation of mouse stem cells into several blood cell types. Our model can successfully infer unobserved CpG methylation states from observations at the same sites in related cell types (90% correct), and this approach more accurately reconstructs missing data than imputation based on neighboring CpGs (84% correct). Additionally, the single CpG resolution of our methylation dynamics estimates enabled us to show that DNA sequence context of CpG sites is informative about methylation dynamics across tissue differentiation. Finally, we identified genomic regions with clusters of highly dynamic CpGs and present a likely functional example. Our work establishes a framework for inference and modeling that is well suited to DNA methylation data, and our success suggests that other methods for analyzing DNA nucleotide substitutions will also translate to the modeling of epigenetic phenomena. Availability and implementation: Source code is available at www.kostkalab.net/software. Contact: tony.capra@vanderbilt.edu or kostka@pitt.edu |
format | Online Article Text |
id | pubmed-4147898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41478982014-09-02 Modeling DNA methylation dynamics with approaches from phylogenetics Capra, John A. Kostka, Dennis Bioinformatics Eccb 2014 Proceedings Papers Committee Motivation: Methylation of CpG dinucleotides is a prevalent epigenetic modification that is required for proper development in vertebrates. Genome-wide DNA methylation assays have become increasingly common, and this has enabled characterization of DNA methylation in distinct stages across differentiating cellular lineages. Changes in CpG methylation are essential to cellular differentiation; however, current methods for modeling methylation dynamics do not account for the dependency structure between precursor and dependent cell types. Results: We developed a continuous-time Markov chain approach, based on the observation that changes in methylation state over tissue differentiation can be modeled similarly to DNA nucleotide changes over evolutionary time. This model explicitly takes precursor to descendant relationships into account and enables inference of CpG methylation dynamics. To illustrate our method, we analyzed a high-resolution methylation map of the differentiation of mouse stem cells into several blood cell types. Our model can successfully infer unobserved CpG methylation states from observations at the same sites in related cell types (90% correct), and this approach more accurately reconstructs missing data than imputation based on neighboring CpGs (84% correct). Additionally, the single CpG resolution of our methylation dynamics estimates enabled us to show that DNA sequence context of CpG sites is informative about methylation dynamics across tissue differentiation. Finally, we identified genomic regions with clusters of highly dynamic CpGs and present a likely functional example. Our work establishes a framework for inference and modeling that is well suited to DNA methylation data, and our success suggests that other methods for analyzing DNA nucleotide substitutions will also translate to the modeling of epigenetic phenomena. Availability and implementation: Source code is available at www.kostkalab.net/software. Contact: tony.capra@vanderbilt.edu or kostka@pitt.edu Oxford University Press 2014-09-01 2014-08-22 /pmc/articles/PMC4147898/ /pubmed/25161227 http://dx.doi.org/10.1093/bioinformatics/btu445 Text en © The Author 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Eccb 2014 Proceedings Papers Committee Capra, John A. Kostka, Dennis Modeling DNA methylation dynamics with approaches from phylogenetics |
title | Modeling DNA methylation dynamics with approaches from phylogenetics |
title_full | Modeling DNA methylation dynamics with approaches from phylogenetics |
title_fullStr | Modeling DNA methylation dynamics with approaches from phylogenetics |
title_full_unstemmed | Modeling DNA methylation dynamics with approaches from phylogenetics |
title_short | Modeling DNA methylation dynamics with approaches from phylogenetics |
title_sort | modeling dna methylation dynamics with approaches from phylogenetics |
topic | Eccb 2014 Proceedings Papers Committee |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147898/ https://www.ncbi.nlm.nih.gov/pubmed/25161227 http://dx.doi.org/10.1093/bioinformatics/btu445 |
work_keys_str_mv | AT caprajohna modelingdnamethylationdynamicswithapproachesfromphylogenetics AT kostkadennis modelingdnamethylationdynamicswithapproachesfromphylogenetics |