Home LiteratureArticle Details
PMID: 17277777 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome.

Nature genetics ·Vol. 39 ·No. 3 ·2007-03-00 ·Pages 311-8

Heintzman ND, Stuart RK, Hon G, Fu Y, Ching CW, Hawkins RD, Barrera LO, Van Calcar S, Qu C, Ching KA, Wang W, Weng Z, Green RD, Crawford GE, Ren B

Abstract

Eukaryotic gene transcription is accompanied by acetylation and methylation of nucleosomes near promoters, but the locations and roles of histone modifications elsewhere in the genome remain unclear. We determined the chromatin modification states in high resolution along 30 Mb of the human genome and found that active promoters are marked by trimethylation of Lys4 of histone H3 (H3K4), whereas enhancers are marked by monomethylation, but not trimethylation, of H3K4. We developed computational algorithms using these distinct chromatin signatures to identify new regulatory elements, predicting over 200 promoters and 400 enhancers within the 30-Mb region. This approach accurately predicted the location and function of independently identified regulatory elements with high sensitivity and specificity and uncovered a novel functional enhancer for the carnitine transporter SLC22A5 (OCTN2). Our results give insight into the connections between chromatin modifications and transcriptional regulatory activity and provide a new tool for the functional annotation of the human genome.

MeSH Terms
Algorithms Chromatin/metabolism Enhancer Elements, Genetic Genome, Human Genomics Histones/metabolism Humans Models, Genetic Organic Cation Transport Proteins/genetics,metabolism Promoter Regions, Genetic Solute Carrier Family 22 Member 5
Chemicals
Chromatin Histones Organic Cation Transport Proteins SLC22A5 protein, human Solute Carrier Family 22 Member 5
Authors & Affiliations
15 authors, click to expand affiliations / ORCID
Heintzman Nathaniel D
Ludwig Institute for Cancer Research, University of California San Diego (UCSD) School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653 USA.
Stuart Rhona K
Hon Gary
Fu Yutao
Ching Christina W
Hawkins R David
Barrera Leah O
Van Calcar Sara
Qu Chunxu
Ching Keith A
Wang Wei
Weng Zhiping
Green Roland D
Crawford Gregory E
Ren Bing
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
Published
2007-03-00
Epub
2007-00-04
Pages
311-8
Language
English
Region
United States
NLM ID
9216904
Subset
IM
Databases
GEO
Corrections
CommentIn
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