首页> 外文期刊>Nature >Histone modifications at human enhancers reflect global cell-type-specific gene expression
【24h】

Histone modifications at human enhancers reflect global cell-type-specific gene expression

机译:人类增强子的组蛋白修饰反映了总体细胞类型特异性基因表达

获取原文
获取原文并翻译 | 示例
       

摘要

The human body is composed of diverse cell types with distinct functions. Although it is known that lineage specification depends on cell-specific gene expression, which in turn is driven by promoters, enhancers, insulators and other cis-regulatory DNA sequences for each gene, the relative roles of these regulatory elements in this process are not clear. We have previously developed a chromatin-immunoprecipitation-based microarray method (ChIP-chip) to locate promoters, enhancers and insulators in the human genome. Here we use the same approach to identify these elements in multiple cell types and investigate their roles in cell-type-specific gene expression. We observed that the chromatin state at promoters and CTCF-binding at insulators is largely invariant across diverse cell types. In contrast, enhancers are marked with highly cell-type-specific histone modification patterns, strongly correlate to cell-type-specific gene expression programs on a global scale, and are functionally active in a cell-type-specific manner. Our results define over 55,000 potential transcriptional enhancers in the human genome, significantly expanding the current catalogue of human enhancers and highlighting the role of these elements in cell-type-specific gene expression.
机译:人体由具有不同功能的多种细胞类型组成。尽管已知谱系规格取决于细胞特异性基因表达,而细胞特异性基因表达又由每个基因的启动子,增强子,绝缘子和其他顺式调控DNA序列驱动,但这些调控元件在此过程中的相对作用尚不清楚。我们以前已经开发了一种基于染色质免疫沉淀的微阵列方法(ChIP芯片),以定位人类基因组中的启动子,增强子和绝缘子。在这里,我们使用相同的方法来识别多种细胞类型中的这些元素,并研究它们在细胞类型特异性基因表达中的作用。我们观察到,启动子处的染色质状态和绝缘子处的CTCF结合在不同类型的细胞中基本不变。相反,增强子以高度细胞类型特异性的组蛋白修饰模式标记,在全球范围内与细胞类型特异性的基因表达程序高度相关,并且以细胞类型特异性的方式起作用。我们的结果定义了人类基因组中超过55,000种潜在的转录增强子,从而大大扩展了人类增强子的当前目录,并突出了这些元素在细胞类型特异性基因表达中的作用。

著录项

  • 来源
    《Nature》 |2009年第7243期|108-112|共5页
  • 作者单位

    Ludwig Institute for Cancer Research, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA Biomedical Sciences Graduate Program, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA;

    Ludwig Institute for Cancer Research, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA Bioinformatics Program, and UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA;

    Ludwig Institute for Cancer Research, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA;

    MIT Computer Science and Artificial Intelligence Laboratory, 32 Vassar Street, Cambridge, Massachusetts 02139, USA;

    MIT Computer Science and Artificial Intelligence Laboratory, 32 Vassar Street, Cambridge, Massachusetts 02139, USA Broad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, Massachusetts 02142, USA;

    Ludwig Institute for Cancer Research, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA;

    Ludwig Institute for Cancer Research, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA;

    Ludwig Institute for Cancer Research, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA;

    Ludwig Institute for Cancer Research, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA;

    Ludwig Institute for Cancer Research, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA;

    Ludwig Institute for Cancer Research, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA;

    Morgridge Institute for Research, Madison, Wisconsin 53707-7365, USA;

    Roche NimbleGen, Inc., 500 South Rosa Road, Madison, Wisconsin 53719, USA;

    Roche NimbleGen, Inc., 500 South Rosa Road, Madison, Wisconsin 53719, USA;

    Roche NimbleGen, Inc., 500 South Rosa Road, Madison, Wisconsin 53719, USA;

    National Institutes of Allergy and Infectious Disease, 5640 Fishers Lane, Rockville, Maryland 20852, USA;

    Morgridge Institute for Research, Madison, Wisconsin 53707-7365, USA;

    Morgridge Institute for Research, Madison, Wisconsin 53707-7365, USA University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin 53706, USA;

    Institute for Genome Sciences and Policy, and Department of Pediatrics, Duke University, 101 Science Drive, Durham, North Carolina 27708, USA;

    MIT Computer Science and Artificial Intelligence Laboratory, 32 Vassar Street, Cambridge, Massachusetts 02139, USA Broad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, Massachusetts 02142, USA;

    Ludwig Institute for Cancer Research, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA Department of Cellular and Molecular Medicine, UCSD School of Medicine, 9500 Gilman Drive, La Jolla, California 92093-0653, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 02:55:32

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号