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Interactome Maps of Mouse Gene Regulatory Domains Reveal Basic Principles of Transcriptional Regulation

机译:小鼠基因调控域的相互作用图揭示了转录调控的基本原理。

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A key finding of the ENCODE project is that the enhancer landscape of mammalian cells undergoes marked alterations during ontogeny. However, the nature and extent of these changes are unclear. As part of the NIH Mouse Regulome Project, we here combined DNasel hypersensitivity, ChIP-seq, and ChIA-PET technologies to map the promoter-enhancer interactomes of pluripotent ES cells and differentiated Β lymphocytes. We confirm that enhancer usage varies widely across tissues. Unexpectedly, we find that this feature extends to broadly transcribed genes, including Myc and Pim1 cell-cycle regulators, which associate with an entirely different set of enhancers in ES and Β cells. By means of high-resolution CpG methylomes, genome editing, and digital footprinting, we show that these enhancers recruit lineage-determining factors. Furthermore, we demonstrate that the turning on and off of enhancers during development correlates with promoter activity. We propose that organisms rely on a dynamic enhancer landscape to control basic cellular functions in a tissue-specific manner.
机译:ENCODE项目的关键发现是哺乳动物细胞的增强子在个体发育过程中发生了明显的变化。但是,这些变化的性质和程度尚不清楚。作为NIH小鼠调控组项目的一部分,我们在这里结合了DNasel超敏反应,ChIP-seq和ChIA-PET技术来绘制多能ES细胞和分化的淋巴细胞的启动子-增强子相互作用组。我们确认增强剂的使用在不同组织之间差异很大。出乎意料的是,我们发现此功能扩展到广泛转录的基因,包括Myc和Pim1细胞周期调节剂,它们与ES和Β细胞中一组完全不同的增强子相关。通过高分辨率的CpG甲基化组,基因组编辑和数字足迹,我们表明这些增强子招募沿袭决定因素。此外,我们证明了在发育过程中增强子的开启和关闭与启动子活性相关。我们建议生物体依靠动态增强剂景观以组织特定的方式控制基本的细胞功能。

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