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CPEB1 a histone-modified hypomethylated gene is regulated by miR-101 and involved in cell senescence in glioma

机译:CPEB1是一种经组蛋白修饰的低甲基化基因受miR-101调控并参与神经胶质瘤的细胞衰老

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摘要

Epigenetic mechanisms have important roles in carcinogenesis. We certified that the mRNA translation-related gene cytoplasmic polyadenylation element-binding protein 1 (CPEB1) is hypomethylated and overexpressed in glioma cells and tissues. The knockdown of CPEB1 reduced cell senescence by regulating the expression or distribution of p53 in glioma cells. CPEB1 is also regulated directly by the tumor suppressor miR-101, a potential marker of glioma. It is known that the histone methyltransferase enhancer of zeste homolog 2 (EZH2) and embryonic ectoderm development (EED) are direct targets of miR-101. We demonstrated that miR-101 downregulated the expression of CPEB1 through reversing the methylation status of the CPEB1 promoter by regulating the presence on the promoter of the methylation-related histones H3K4me2, H3K27me3, H3K9me3 and H4K20me3. The epigenetic regulation of H3K27me3 on CPEB1 promoter is mediated by EZH2 and EED. EZH2 has a role in the regulation of H3K4me2. Furthermore, the downregulation of CPEB1 induced senescence in a p53-dependent manner.
机译:表观遗传机制在致癌作用中具有重要作用。我们证明,mRNA翻译相关基因胞质多腺苷酸化元素结合蛋白1(CPEB1)被低甲基化,并在神经胶质瘤细胞和组织中过表达。通过调节神经胶质瘤细胞中p53的表达或分布,敲低CPEB1可以减少细胞衰老。 CPEB1还直接受肿瘤抑制物miR-101(神经胶质瘤的潜在标志物)直接调控。众所周知,zeste同源物2(EZH2)的组蛋白甲基转移酶增强子和胚胎外胚层发育(EED)是miR-101的直接靶标。我们证明,miR-101通过调节甲基化相关组蛋白H3K4me2,H3K27me3,H3K9me3和H4K20me3在启动子上的存在来逆转CPEB1启动子的甲基化状态,从而下调CPEB1的表达。 H3K27me3对CPEB1启动子的表观遗传调控是由EZH2和EED介导的。 EZH2在H3K4me2的调控中起作用。此外,CPEB1的下调以p53依赖的方式诱导衰老。

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