Literature DB >> 18656446

Histone methylation marks play important roles in predicting the methylation status of CpG islands.

Shicai Fan1, Michael Q Zhang, Xuegong Zhang.   

Abstract

The methylation status of CpG islands is highly correlated with gene expression. Current methods for computational prediction of DNA methylation only utilize DNA sequence features. In this study, besides 35 DNA sequence features, we added four histone methylation marks to predict the methylation status of CpG islands, and improved the accuracy to 89.94%. Also we applied our model to predict the methylation pattern of all the CpG islands in the human genome, and the results are consistent with the previous reports. Our results imply the important roles of histone methylation marks in affecting the methylation status of CpG islands. H3K4me enriched in the methylation-resistant CpG islands could disrupt the contacts between nucleosomes, unravel chromatin and make DNA sequences accessible. And the established open environment may be a prerequisite for or a consequence of the function implementation of zinc finger proteins that could protect CpG islands from DNA methylation.

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Year:  2008        PMID: 18656446      PMCID: PMC2974564          DOI: 10.1016/j.bbrc.2008.07.077

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  32 in total

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5.  CpG islands in vertebrate genomes.

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  21 in total

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5.  Introduction--Epiphanies in epigenetics.

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Review 6.  Molecular coupling of DNA methylation and histone methylation.

Authors:  Hideharu Hashimoto; Paula M Vertino; Xiaodong Cheng
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7.  Interactions between core histone marks and DNA methyltransferases predict DNA methylation patterns observed in human cells and tissues.

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Journal:  Epigenetics       Date:  2019-09-17       Impact factor: 4.528

8.  CpG_MI: a novel approach for identifying functional CpG islands in mammalian genomes.

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10.  CpGIMethPred: computational model for predicting methylation status of CpG islands in human genome.

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