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

被引:2617
作者
Heintzman, Nathaniel D.
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
机构
[1] Univ Calif San Diego, Sch Med, Ludwig Inst Canc Res, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Sch Med, Biomed Sci Grad Program, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Sch Med, Program Bioinformat, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Sch Med, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[5] Boston Univ, Bioinformat Program, Boston, MA 02215 USA
[6] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[7] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[8] NimbleGen Syst Inc, Madison, WI 53711 USA
[9] Duke Univ, Inst Genome Sci & Policy, Durham, NC 27708 USA
[10] Duke Univ, Dept Pediat, Durham, NC 27708 USA
关键词
D O I
10.1038/ng1966
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
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.
引用
收藏
页码:311 / 318
页数:8
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