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An insulator element 3' to the CFTR gene binds CTCF and reveals an active chromatin hub in primary cells

机译:CFTR基因的绝缘子元件3'与CTCF结合并在原代细胞中显示出活跃的染色质中心

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Regulation of expression of the CFTR gene is poorly understood. Elements within the basal promoter of the gene do not fully explain CFTR expression patterns, suggesting that cis-regulatory elements are located elsewhere, either within the locus or in adjacent chromatin. We previously mapped DNase I hypersensitive sites (DHS) in 400 kb spanning the CFTR locus including a cluster of sites close to the 3'-end of the gene. Here we focus on a DHS at +6.8 kb from the CFTR translation end-point to evaluate its potential role in regulating expression of the gene. This DHS, which encompasses a consensus CTCF-binding site, was evident in primary human epididymis cells that express abundant CFTR mRNA. We show by DNase I footprinting and electophoretic mobility shift assays that the cis-regulatory element within this DHS binds CTCF in vitro. We further demonstrate that the element functions as an enhancer blocker in a well-established in vivo assay, and by using chromatin immunoprecipitation that it recruits CTCF in vivo. Moreover, we reveal that in primary epididymis cells, the +6.8 kb DHS interacts closely with the CFTR promoter, suggesting that the CFTR locus exists in a looped conformation, characteristic of an active chromatin hub.
机译:CFTR基因表达的调控了解甚少。基因基础启动子中的元件不能完全解释CFTR的表达方式,表明顺式调控元件位于基因座内或邻近染色质的其他位置。我们先前在跨越CFTR基因座的400 kb中绘制了DNase I超敏位点(DHS),其中包括靠近该基因3'端的一系列位点。在这里,我们将重点放在距离CFTR翻译终点+6.8 kb的DHS上,以评估其在调节基因表达中的潜在作用。该DHS包含一个共有的CTCF结合位点,在表达大量CFTR mRNA的原代人附睾细胞中很明显。我们通过DNase I足迹和电子迁移率迁移分析表明,该DHS中的顺式调节元件在体外与CTCF结合。我们进一步证明,该元素在成熟的体内测定中起着增强剂阻断剂的作用,并通过使用染色质免疫沉淀在体内募集CTCF。此外,我们发现在原发附睾细胞中,+ 6.8 kb DHS与CFTR启动子紧密相互作用,这表明CFTR基因座以环状构象存在,这是活性染色质集线器的特征。

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