Cancer Science Institute of Singapore and.
Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Blood. 2019 Jun 6;133(23):2507-2517. doi: 10.1182/blood.2018886077. Epub 2019 Apr 5.
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.
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。