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ABCC6 的表达受 CCAAT/增强子结合蛋白调节,该蛋白激活位于基因第一内含子中的灵长类特异性序列。

ABCC6 expression is regulated by CCAAT/enhancer-binding protein activating a primate-specific sequence located in the first intron of the gene.

机构信息

Laboratory of Transcriptional Regulation, Institute of Medical Biology, Polish Academy of Sciences, Lodz, Poland.

出版信息

J Invest Dermatol. 2012 Dec;132(12):2709-17. doi: 10.1038/jid.2012.218. Epub 2012 Jul 5.

Abstract

Pseudoxanthoma elasticum (PXE), a rare recessive genetic disease causing skin, eye, and cardiovascular lesions, is characterized by the calcification of elastic fibers. The disorder is due to loss-of-function mutations of the ABCC6 gene, but the pathophysiology of the disease is still not understood. Here we investigated the transcriptional regulation of the gene, using DNase I hypersensitivity assay followed by luciferase reporter gene assay. We identified three DNase I hypersensitive sites (HSs) specific to cell lines expressing ABCC6. These HSs are located in the proximal promoter and in the first intron of the gene. We further characterized the role of the HSs by luciferase assay and demonstrated the transcriptional activity of the intronic HS. We identified the CCAAT/enhancer-binding protein β (C/EBPβ) as a factor binding the second intronic HS by chromatin immunoprecipitation and corroborated this finding by luciferase assays. We also showed that C/EBPβ interacts with the proximal promoter of the gene. We propose that C/EBPβ forms a complex with other regulatory proteins including the previously identified regulatory factor hepatocyte nuclear factor 4α (HNF4α). This complex would account for the tissue-specific expression of the gene and might serve as a metabolic sensor. Our results point toward a better understanding of the physiological role of ABCC6.

摘要

弹性假黄瘤(PXE)是一种罕见的隐性遗传疾病,可导致皮肤、眼睛和心血管损伤,其特征是弹性纤维钙化。该疾病是由于 ABCC6 基因的功能丧失突变引起的,但疾病的病理生理学仍不清楚。在这里,我们使用 DNase I 超敏反应检测 followed by luciferase 报告基因检测来研究该基因的转录调控。我们鉴定了三个特定于表达 ABCC6 的细胞系的 DNase I 超敏位点(HS)。这些 HS 位于基因的近端启动子和第一内含子中。我们通过荧光素酶测定进一步表征了 HS 的作用,并证明了内含子 HS 的转录活性。我们通过染色质免疫沉淀鉴定了 CCAAT/增强子结合蛋白 β(C/EBPβ)作为结合第二个内含子 HS 的因子,并通过荧光素酶测定证实了这一发现。我们还表明,C/EBPβ与基因的近端启动子相互作用。我们提出,C/EBPβ与包括先前鉴定的调节因子肝细胞核因子 4α(HNF4α)在内的其他调节蛋白形成复合物。该复合物将解释基因的组织特异性表达,并可能作为代谢传感器。我们的研究结果为更好地理解 ABCC6 的生理作用提供了线索。

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