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PMID: 18552846 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural Research Support, Non-U.S. Gov't

Combinatorial patterns of histone acetylations and methylations in the human genome.

Nature genetics ·Vol. 40 ·No. 7 ·2008-07-00 ·Pages 897-903

Wang Z, Zang C, Rosenfeld JA, Schones DE, Barski A, Cuddapah S, Cui K, Roh TY, Peng W, Zhang MQ, Zhao K

Abstract

Histones are characterized by numerous posttranslational modifications that influence gene transcription. However, because of the lack of global distribution data in higher eukaryotic systems, the extent to which gene-specific combinatorial patterns of histone modifications exist remains to be determined. Here, we report the patterns derived from the analysis of 39 histone modifications in human CD4(+) T cells. Our data indicate that a large number of patterns are associated with promoters and enhancers. In particular, we identify a common modification module consisting of 17 modifications detected at 3,286 promoters. These modifications tend to colocalize in the genome and correlate with each other at an individual nucleosome level. Genes associated with this module tend to have higher expression, and addition of more modifications to this module is associated with further increased expression. Our data suggest that these histone modifications may act cooperatively to prepare chromatin for transcriptional activation.

MeSH Terms
Acetylation Cells, Cultured Chromosome Mapping Cluster Analysis Enhancer Elements, Genetic Genome, Human/physiology Histone Acetyltransferases/metabolism Histone Methyltransferases Histone-Lysine N-Methyltransferase/metabolism Histones/metabolism Humans Methylation Promoter Regions, Genetic Protein Binding Protein Methyltransferases
Chemicals
Histones Histone Methyltransferases Protein Methyltransferases Histone-Lysine N-Methyltransferase Histone Acetyltransferases
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Wang Zhibin
Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute, US National Institutes of Health, Bethesda, Maryland 20892, USA.
Zang Chongzhi
Rosenfeld Jeffrey A
Schones Dustin E
Barski Artem
Cuddapah Suresh
Cui Kairong
Roh Tae-Young
Peng Weiqun
Zhang Michael Q
Zhao Keji
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Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1546-1718
Published
2008-07-00
Epub
2008-00-15
Pages
897-903
Language
English
Region
United States
NLM ID
9216904
PMCID
PMC2769248
Subset
IM
Grants
NHGRI NIH HHS · R01 HG001696 · United States
NHGRI NIH HHS · R01 HG001696-05 · United States
Intramural NIH HHS · Z01 HL005801-05 · United States
NHGRI NIH HHS · HG001696 · United States
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