Profile analysis and prediction of tissue-specific CpG island methylation classes

<p>Abstract</p> <p>Background</p> <p>The computational prediction of DNA methylation has become an important topic in the recent years due to its role in the epigenetic control of normal and cancer-related processes. While previous prediction approaches focused merely o...

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Main Authors: Zwir Igor, Harari Oscar, Previti Christopher, del Val Coral
Format: Article
Language:English
Published: BMC 2009-04-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/10/116
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spelling doaj-edeeec112cb24b478a05a68377fff6842020-11-24T21:56:32ZengBMCBMC Bioinformatics1471-21052009-04-0110111610.1186/1471-2105-10-116Profile analysis and prediction of tissue-specific CpG island methylation classesZwir IgorHarari OscarPreviti Christopherdel Val Coral<p>Abstract</p> <p>Background</p> <p>The computational prediction of DNA methylation has become an important topic in the recent years due to its role in the epigenetic control of normal and cancer-related processes. While previous prediction approaches focused merely on differences between methylated and unmethylated DNA sequences, recent experimental results have shown the presence of much more complex patterns of methylation across tissues and time in the human genome. These patterns are only partially described by a binary model of DNA methylation. In this work we propose a novel approach, based on profile analysis of tissue-specific methylation that uncovers significant differences in the sequences of CpG islands (CGIs) that predispose them to a tissue- specific methylation pattern.</p> <p>Results</p> <p>We defined CGI methylation profiles that separate not only between constitutively methylated and unmethylated CGIs, but also identify CGIs showing a differential degree of methylation across tissues and cell-types or a lack of methylation exclusively in sperm. These profiles are clearly distinguished by a number of CGI attributes including their evolutionary conservation, their significance, as well as the evolutionary evidence of prior methylation. Additionally, we assess profile functionality with respect to the different compartments of protein coding genes and their possible use in the prediction of DNA methylation.</p> <p>Conclusion</p> <p>Our approach provides new insights into the biological features that determine if a CGI has a functional role in the epigenetic control of gene expression and the features associated with CGI methylation susceptibility. Moreover, we show that the ability to predict CGI methylation is based primarily on the quality of the biological information used and the relationships uncovered between different sources of knowledge. The strategy presented here is able to predict, besides the constitutively methylated and unmethylated classes, two more tissue specific methylation classes conserving the accuracy provided by leading binary methylation classification methods.</p> http://www.biomedcentral.com/1471-2105/10/116
collection DOAJ
language English
format Article
sources DOAJ
author Zwir Igor
Harari Oscar
Previti Christopher
del Val Coral
spellingShingle Zwir Igor
Harari Oscar
Previti Christopher
del Val Coral
Profile analysis and prediction of tissue-specific CpG island methylation classes
BMC Bioinformatics
author_facet Zwir Igor
Harari Oscar
Previti Christopher
del Val Coral
author_sort Zwir Igor
title Profile analysis and prediction of tissue-specific CpG island methylation classes
title_short Profile analysis and prediction of tissue-specific CpG island methylation classes
title_full Profile analysis and prediction of tissue-specific CpG island methylation classes
title_fullStr Profile analysis and prediction of tissue-specific CpG island methylation classes
title_full_unstemmed Profile analysis and prediction of tissue-specific CpG island methylation classes
title_sort profile analysis and prediction of tissue-specific cpg island methylation classes
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2009-04-01
description <p>Abstract</p> <p>Background</p> <p>The computational prediction of DNA methylation has become an important topic in the recent years due to its role in the epigenetic control of normal and cancer-related processes. While previous prediction approaches focused merely on differences between methylated and unmethylated DNA sequences, recent experimental results have shown the presence of much more complex patterns of methylation across tissues and time in the human genome. These patterns are only partially described by a binary model of DNA methylation. In this work we propose a novel approach, based on profile analysis of tissue-specific methylation that uncovers significant differences in the sequences of CpG islands (CGIs) that predispose them to a tissue- specific methylation pattern.</p> <p>Results</p> <p>We defined CGI methylation profiles that separate not only between constitutively methylated and unmethylated CGIs, but also identify CGIs showing a differential degree of methylation across tissues and cell-types or a lack of methylation exclusively in sperm. These profiles are clearly distinguished by a number of CGI attributes including their evolutionary conservation, their significance, as well as the evolutionary evidence of prior methylation. Additionally, we assess profile functionality with respect to the different compartments of protein coding genes and their possible use in the prediction of DNA methylation.</p> <p>Conclusion</p> <p>Our approach provides new insights into the biological features that determine if a CGI has a functional role in the epigenetic control of gene expression and the features associated with CGI methylation susceptibility. Moreover, we show that the ability to predict CGI methylation is based primarily on the quality of the biological information used and the relationships uncovered between different sources of knowledge. The strategy presented here is able to predict, besides the constitutively methylated and unmethylated classes, two more tissue specific methylation classes conserving the accuracy provided by leading binary methylation classification methods.</p>
url http://www.biomedcentral.com/1471-2105/10/116
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AT previtichristopher profileanalysisandpredictionoftissuespecificcpgislandmethylationclasses
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