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Carnosine influences transcription via epigenetic regulation as demonstrated by enhanced histone acetylation of the pyruvate dehydrogenase kinase 4 promoter in glioblastoma cells

机译:通过增强胶合盐脱氢酶激酶4启动子在胶质母细胞瘤细胞中的增强组蛋白乙酰化,影响转录通过表观遗传调控的转录

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摘要

Carnosine (-alanyl-l-histidine) affects a plethora of signaling pathways and genes in different biological systems. Although known as a radical scavenger, not all of these effects can simply be ascribed to its chemical nature. As previous experiments pointed towards the possibility that carnosine affects epigenetic regulation via histone acetylation, we investigated this hypothesis using the glioblastoma cell lines U87 and T98G in which carnosine's anti-neoplastic effect is accompanied by increased expression of pyruvate dehydrogenase kinase 4. Viability and expression of PDK4 was analyzed after incubation in carnosine and different histone deacetylase inhibitors (HDACi) using cell-based assays and qRT-PCR. In addition, chromatin immunoprecipitation (ChIP) experiments were performed and the global influence of carnosine on histone H3 acetylation was analyzed by Western blot. Carnosine as well as the HDACi used increased expression of PDK4. In addition, all compounds reduced cell viability, although differences were observed with regard to magnitude and required concentrations. ChIP analysis revealed increased acetylation of histone H3 in the PDK4 promoter of U87 and T98G cells (similar to 1.3- and similar to 1.7-fold, respectively) 6h after the addition of carnosine (50mM) followed by increased expression of PDK4 mRNA. Western blots did not detect a general increase of H3 acetylation at a genome-wide scale under the influence of carnosine. Our experiments for the first time demonstrate that carnosine influences epigenetic regulation via increased histone acetylation.
机译:肉核苷酸( - alanyl-L-组氨酸)影响不同生物系统中的一定的信号传导途径和基因。虽然被称为激进的清除剂,但并非所有这些效果都可以简单地归因于其化学性质。作为先前的实验,指出肉核苷酸通过组蛋白乙酰化影响表观遗传调节,我们使用胶质母细胞瘤细胞系U87和T98G研究了该假设,其中肉毒肽的抗肿瘤效果伴随着丙酮酸脱氢酶激酶4的表达增加了4.活力和表达使用基于细胞的测定和QRT-PCR在肉毒肽和不同组蛋白脱乙酰酶抑制剂(HDACI)中孵育后分析PDK4。此外,通过蛋白质印迹分析染色质免疫沉淀(Chip)实验,并通过Western印迹分析了肉毒肽对组蛋白H3乙酰化的全局影响。肉核苷酸以及HDACI使用的PDK4表达增加。此外,所有化合物都降低了细胞活力,但在幅度和所需浓度方面观察到差异。芯片分析显示,在加入肉毒肽(50mm)后,​​在U87和T98G细胞的PDK4启动子中,在U87和T98G细胞的PDK4启动子中的组蛋白H3的乙酰化增加(分别为1.3倍)6小时,然后增加PDK4 mRNA的表达。蛋白质印迹未在肉核苷的影响下以基因组规模探测H3乙酰化的一般增加。我们首次进行实验表明肉核苷酸通过增加的组蛋白乙酰化影响表观遗传调节。

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