Article abstract


Nature Genetics 39, 311 - 318 (2007)
Published online: 4 February 2007 | doi:10.1038/ng1966

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

Nathaniel D Heintzman1,2, Rhona K Stuart1, Gary Hon1,3, Yutao Fu4, Christina W Ching1, R David Hawkins1, Leah O Barrera1,3, Sara Van Calcar1, Chunxu Qu1, Keith A Ching1, Wei Wang5, Zhiping Weng4,6, Roland D Green7, Gregory E Crawford8 & Bing Ren1,9


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.

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  1. Ludwig Institute for Cancer Research, University of California San Diego (UCSD) School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653 USA.
  2. Biomedical Sciences Graduate Program, University of California San Diego (UCSD) School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653 USA.
  3. Program in Bioinformatics and University of California San Diego (UCSD) School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653 USA.
  4. Bioinformatics Program, Boston University, 24 Cummington Street, 1002, Boston, Massachusetts 02215 USA.
  5. Department of Chemistry and Biochemistry, UCSD, 9500 Gilman Drive, La Jolla, California 92093 USA.
  6. Biomedical Engineering Department, Boston University, 44 Cummington Street, Boston, MA 02215.
  7. NimbleGen Systems, Inc., 1 Science Court, Madison, Wisconsin 53711 USA.
  8. Institute for Genome Sciences & Policy and Department of Pediatrics, Duke University, 101 Science Drive, Durham, North Carolina 27708, USA.
  9. Department of Cellular and Molecular Medicine, University of California San Diego (UCSD) School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653 USA.

Correspondence to: Bing Ren1,9 e-mail: biren@ucsd.edu

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