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鉴定 CEBPE 必需的新型增强子在粒细胞分化中的作用。

Identification of a novel enhancer of CEBPE essential for granulocytic differentiation.

机构信息

Cancer Science Institute of Singapore and.

Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

出版信息

Blood. 2019 Jun 6;133(23):2507-2517. doi: 10.1182/blood.2018886077. Epub 2019 Apr 5.

Abstract

CCAAT/enhancer binding protein ε (CEBPE) is an essential transcription factor for granulocytic differentiation. Mutations of occur in individuals with neutrophil-specific granule deficiency (SGD), which is characterized by defects in neutrophil maturation. -knockout mice also exhibit defects in terminal differentiation of granulocytes, a phenotype reminiscent of SGD. Analysis of DNase I hypersensitive sites sequencing data revealed an open chromatin region 6 kb downstream of the transcriptional start site of in murine myeloid cells. We identified an interaction between this +6-kb region and the core promoter of using circular chromosome conformation capture sequencing (4C-seq). To understand the role of this putative enhancer in transcriptional regulation of , we targeted it using catalytically inactive Cas9 fused to Krüppel-associated box (KRAB) domain and observed a significant downregulation of transcript and protein levels of CEBPE in cells expressing guide RNA targeting the +6-kb region. To further investigate the role of this novel enhancer further in myelopoiesis, we generated mice with deletion of this region using CRISPR/Cas9 technology. Germline deletion of the +6-kb enhancer resulted in reduced levels of CEBPE and its target genes and caused a severe block in granulocytic differentiation. We also identified binding of CEBPA and CEBPE to the +6-kb enhancer, which suggests their role in regulating the expression of In summary, we have identified a novel enhancer crucial for regulating expression of and required for normal granulocytic differentiation.

摘要

CCAAT/增强子结合蛋白ε(CEBPE)是粒细胞分化所必需的转录因子。在中性粒细胞特异性颗粒缺乏症(SGD)患者中发生 突变,其特征是中性粒细胞成熟缺陷。-敲除小鼠也表现出粒细胞终末分化缺陷,表现为 SGD 表型。DNase I 超敏位点测序数据分析显示,在鼠髓样细胞中,转录起始位点下游 处存在一个开放染色质区域。我们使用环形染色体构象捕获测序(4C-seq)鉴定了该+6-kb 区域与 核心启动子之间的相互作用。为了了解该假定增强子在 转录调控中的作用,我们使用与 Krüppel 相关盒(KRAB)结构域融合的失活 Cas9 靶向该区域,并观察到靶向+6-kb 区域的指导 RNA 表达的细胞中 CEBPE 的转录本和蛋白水平显著下调。为了进一步研究该新型增强子在髓样细胞生成中的作用,我们使用 CRISPR/Cas9 技术在小鼠中缺失该区域。该+6-kb 增强子的种系缺失导致 CEBPE 及其靶基因水平降低,并导致粒细胞分化严重受阻。我们还鉴定了 CEBPA 和 CEBPE 与+6-kb 增强子的结合,这表明它们在调节 表达中的作用。总之,我们已经确定了一个新的增强子对于调节 表达至关重要,并且对于正常的粒细胞分化是必需的。

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