首页> 美国卫生研究院文献>Orphanet Journal of Rare Diseases >Expression of the SERPING1 gene is not regulated by promoter hypermethylation in peripheral blood mononuclear cells from patients with hereditary angioedema due to C1-inhibitor deficiency
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Expression of the SERPING1 gene is not regulated by promoter hypermethylation in peripheral blood mononuclear cells from patients with hereditary angioedema due to C1-inhibitor deficiency

机译:C1抑制剂缺乏导致遗传性血管性水肿患者外周血单个核细胞中SERPING1基因的表达不受启动子高甲基化的调节

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摘要

SERPING1 mutations causing Hereditary Angioedema type I (HAE-I) due to C1-Inhibitor (C1-INH) deficiency display a dominant-negative effect usually resulting in protein levels far below the expected 50%. To further investigate mechanisms for its reduced expression, we analyzed the promoter DNA methylation status of SERPING1 and its influence on C1-INH expression. Global epigenetic reactivation correlated with C1-INH mRNA synthesis and protein secretion in Huh7 hepatoma cells. However, PBMCs extracted from controls, HAE-I and HAE-II patients presented identical methylation status of the SERPING1 promoter when analyzed by bisulphite sequencing; the proximal CpG island (exon 2) is constitutively unmethylated, while the most distant one (5.7Kb upstream the transcriptional start site) is fully methylated. These results correlate with the methylation profile observed in Huh7 cells and indicate that there is not a direct epigenetic regulation of C1-INH expression in PBMCs specific for each HAE type. Other indirect modes of epigenetic regulation cannot be excluded.
机译:由于C1抑制剂(C1-INH)缺乏而导致I型遗传性血管性水肿(SERE1)的SERPING1突变显示出显性负作用,通常导致蛋白质水平远低于预期的50%。为了进一步研究其减少表达的机制,我们分析了SERPING1的启动子DNA甲基化状态及其对C1-INH表达的影响。全局表观遗传激活与Huh7肝癌细胞中C1-INH mRNA的合成和蛋白分泌有关。然而,当通过亚硫酸氢盐测序进行分析时,从对照,HAE-I和HAE-II患者中提取的PBMC呈现出SERPING1启动子相同的甲基化状态。近端CpG岛(外显子2)组成性未甲基化,而最远的CpG岛(转录起始位点上游5.7Kb)完全甲基化。这些结果与在Huh7细胞中观察到的甲基化谱图相关,表明在每种HAE类型特异性的PBMC中,C1-INH表达没有直接的表观遗传调控。表观遗传调控的其他间接模式不能排除。

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