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Cited by 750

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains

Open access
Rakyan, Vardhman K., Down, Thomas A., Maslau, Siarhei, Andrew, Toby, Yang, Tsun-Po, Beyan, Huriya, Whittaker, Pamela, McCann, Owen T., Finer, Sarah, Valdes, Ana M., Leslie, R. David, Deloukas, Panogiotis, Spector, Timothy D.·2010·Genome Research

Abstract

There is a growing realization that some aging-associated phenotypes/diseases have an epigenetic basis. Here, we report the first genome-scale study of epigenomic dynamics during normal human aging. We identify aging-associated differentially methylated regions (aDMRs) in whole blood in a discovery cohort, and then replicate these aDMRs in sorted CD4+ T-cells and CD14+ monocytes in an independent cohort, suggesting that aDMRs occur in precursor haematopoietic cells. Further replication of the aDMRs in buccal cells, representing a tissue that originates from a different germ layer compared with blood, demonstrates that the aDMR signature is a multitissue phenomenon. Moreover, we demonstrate that aging-associated DNA hypermethylation occurs predominantly at bivalent chromatin domain promoters. This same category of promoters, associated with key developmental genes, is frequently hypermethylated in cancers and in vitro cell culture, pointing to a novel mechanistic link between aberrant hypermethylation in cancer, aging, and cell culture.

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Crossref · 10.1101/gr.103101.109

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Metadata

Authors
Rakyan, V. K., Down, T. A., Maslau, S., Andrew, T., Yang, T.-P., Beyan, H., Whittaker, P., McCann, O. T., Finer, S., Valdes, A. M., Leslie, R. D., Deloukas, P., & Spector, T. D.
Venue
Genome Research
Published
2010-03-10
Volume
20
Issue
4
Pages
434-439
ISSN
1088-9051 (ISSN-L)
OpenAlex
W2039669402
Cited by
750
References
9
Type
posted content
Language
en
Open access
bronze

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