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首页> 外文期刊>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:由于C1抑制剂缺乏,来自遗传性血型血症患者的外周血单核细胞中的促进剂高甲基化不调节六种基因的表达

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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)缺乏导致遗传性血管型型I(HAE-I)的序列1突变显示出显性阴性效应,通常导致蛋白质水平远低于预期的50%。为了进一步研究其降低的表达机制,我们分析了六型甲基甲基化状态的促进剂DNA甲基化状态及其对C1-INH表达的影响。全局表观遗传反应与HuH7肝细胞瘤细胞中的C1-InH mRNA合成和蛋白质分泌相关。然而,在通过双硫酸氢膦序列测序分析时,从对照,HAE-I和HAE-II患者中提取的PBMCS呈现出六种启动子的相同甲基化状态;近端CPG岛(外显子2)组成型未甲基化,而最远的近距离(转录起始位点上游5.7Kb)是完全甲基化的。这些结果与HuH7细胞中观察到的甲基化曲线相关,并表明在每种海型的PBMC中没有在PBMC中的C1-INH表达的直接表观调节。不能排除其他间接调节的间接模式。

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