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人类基因组中转录启动子和增强子独特且具有预测性的染色质特征

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

作者信息

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

机构信息

Ludwig Institute for Cancer Research, University of California San Diego (UCSD) School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653 USA.

出版信息

Nat Genet. 2007 Mar;39(3):311-8. doi: 10.1038/ng1966. Epub 2007 Feb 4.

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.

摘要

真核基因转录伴随着启动子附近核小体的乙酰化和甲基化,但基因组中其他位置的组蛋白修饰的定位和作用仍不清楚。我们沿着人类基因组的30兆碱基对以高分辨率确定了染色质修饰状态,发现活性启动子以组蛋白H3的赖氨酸4(H3K4)三甲基化为标志,而增强子以H3K4单甲基化而非三甲基化为标志。我们利用这些不同的染色质特征开发了计算算法来识别新的调控元件,预测了30兆碱基对区域内超过200个启动子和400个增强子。这种方法以高灵敏度和特异性准确预测了独立鉴定的调控元件的位置和功能,并发现了肉碱转运蛋白SLC22A5(OCTN2)的一个新的功能性增强子。我们的结果深入了解了染色质修饰与转录调控活性之间的联系,并为人类基因组的功能注释提供了一种新工具。

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