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A genome-wide screen in human embryonic stem cells reveals novel sites of allele-specific histone modification associated with known disease loci.

TitleA genome-wide screen in human embryonic stem cells reveals novel sites of allele-specific histone modification associated with known disease loci.
Publication TypeJournal Article
Year of Publication2012
AuthorsPrendergast, JGD, Tong, P, Hay, DC, Farrington, SM, Semple, CAM
JournalEpigenetics Chromatin
Volume5
Issue1
Pagination6
Date Published2012
ISSN1756-8935
Abstract

BACKGROUND: Chromatin structure at a given site can differ between chromosome copies in a cell, and such imbalances in chromatin structure have been shown to be important in understanding the molecular mechanisms controlling several disease loci. Human genetic variation, DNA methylation, and disease have been intensely studied, uncovering many sites of allele-specific DNA methylation (ASM). However, little is known about the genome-wide occurrence of sites of allele-specific histone modification (ASHM) and their relationship to human disease. The aim of this study was to investigate the extent and characteristics of sites of ASHM in human embryonic stem cells (hESCs).

RESULTS: Using a statistically rigorous protocol, we investigated the genomic distribution of ASHM in hESCs, and their relationship to sites of allele-specific expression (ASE) and DNA methylation. We found that, although they were rare, sites of ASHM were substantially enriched at loci displaying ASE. Many were also found at known imprinted regions, hence sites of ASHM are likely to be better markers of imprinted regions than sites of ASM. We also found that sites of ASHM and ASE in hESCs colocalize at risk loci for developmental syndromes mediated by deletions, providing insights into the etiology of these disorders.

CONCLUSION: These results demonstrate the potential importance of ASHM patterns in the interpretation of disease loci, and the protocol described provides a basis for similar studies of ASHM in other cell types to further our understanding of human disease susceptibility.

DOI10.1186/1756-8935-5-6
Alternate JournalEpigenetics Chromatin
PubMed ID22607690
PubMed Central IDPMC3438052

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