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Lineage-specific dynamic and pre-established enhancer-promoter contacts cooperate in terminal differentiation

机译:谱系特异性动态和预先建立的增强剂 - 启动子触点在终端分化中配合

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摘要

Chromosome conformation is an important feature of metazoan gene regulation(1,2); however, enhancer-promoter contact remodeling during cellular differentiation remains poorly understood(3). To address this, genome-wide promoter capture Hi-C (CHi-C) (1,4) was performed during epidermal differentiation(5). Two classes of enhancer-promoter contacts associated with differentiation-induced genes were identified. The first class ('gained') increased in contact strength during differentiation in concert with enhancer acquisition of the H3K27ac activation mark. The second class ('stable') were pre-established in undifferentiated cells, with enhancers constitutively marked by H3K27ac. The stable class was associated with the canonical conformation regulator cohesin, whereas the gained class was not, implying distinct mechanisms of contact formation and regulation. Analysis of stable enhancers identified a new, essential role for a constitutively expressed, lineage-restricted ETS-family transcription factor, EHF, in epidermal differentiation. Furthermore, neither class of contacts was observed in pluripotent cells, suggesting that lineage-specific chromatin structure is established in tissue progenitor cells and is further remodeled in terminal differentiation.
机译:染色体构象是甲氧烷基因调控的重要特征(1,2);然而,在细胞分化期间的增强剂 - 启动子接触重塑仍然是较差的(3)。为了解决这一点,在表皮分化(5)期间进行基因组 - 宽的启动子捕获HI-C(CHI-C)(1,4)。鉴定了与分化诱导基因相关的两类增强剂 - 启动子接触。第一类('获得')在分化期间的接触强度随着H3K27AC活化标记的增强剂的次数分化。在未分化的细胞中预先建立了第二类('稳定'),增强剂由H3K27Ac构成型标记。稳定的阶级与规范构象调节器咖啡蛋白有关,而所需的类别不是暗示不同的接触形成和调节机制。稳定增强剂分析确定了组成型表达,谱系限制的ETS家族转录因子,EHF,表皮分化的新的重要作用。此外,在多能细胞中没有观察到触点,表明在组织祖细胞中建立了谱系特异性染色质结构,并且在末端分化中进一步改造。

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