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Egr-1 regulates the transcription of NGX6 gene through a Sp1/Egr-1 overlapping site in the promoter

机译:Egr-1通过启动子中的Sp1 / Egr-1重叠位点调节NGX6基因的转录

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As a novel candidate metastasis suppressor gene, Nasopharyngeal carcinoma-associated gene 6 (NGX6) is involved in cellular growth, cell cycle progression and tumor angiogenesis. Previous studies have shown that NGX6 gene is down-regulated in colorectal cancer (CRC). However, little is known about its transcriptional regulation. We defined the minimal promoter of NGX6 gene in a 186-bp region (from-86 to +100) through mutation construct methods and luciferase assays. Results from Electrophoretic mobility shift assays (EMSA) and Chromatin immunoprecipitation (ChIP) revealed that Early growth response gene 1 (Egr-1) binds to the Sp1/Egr-1 overlapping site of NGX6 minimal promoter. Overexpression of Egr-1 increased the promoter activity and mRNA level of NGX6 gene; while knock-down of endogenous Egr-1 decreased mRNA expression of NGX6 gene. These results demonstrate that Egr-1 regulates NGX6 gene transcription through an overlapping Sp1/Egr-1 binding site as a positive regulator of NGX6 gene.
机译:作为一种新型的候选转移抑制基因,鼻咽癌相关基因6(NGX6)参与细胞生长,细胞周期进程和肿瘤血管生成。先前的研究表明,NGX6基因在大肠癌(CRC)中被下调。但是,对其转录调控知之甚少。通过突变构建方法和荧光素酶测定,我们在186-bp区域(从-86到+100)中定义了NGX6基因的最小启动子。电泳迁移率变动分析(EMSA)和染色质免疫沉淀(ChIP)的结果表明,早期生长反应基因1(Egr-1)与NGX6最小启动子的Sp1 / Egr-1重叠位点结合。 Egr-1的过表达增加了NGX6基因的启动子活性和mRNA水平。内源性Egr-1的敲低降低了NGX6基因的mRNA表达。这些结果表明,Egr-1通过重叠的Sp1 / Egr-1结合位点作为NGX6基因的正向调节剂来调节NGX6基因的转录。

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