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AKT1 的启动子和 3'-UTR 中的 G-四链体正向调控其活性。

AKT1 is positively regulated by G-quadruplexes in its promoter and 3'-UTR.

机构信息

Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Ministry of Education, College of Life Science, Northeast Forestry University, Harbin, 150040, China.

College of Arts and Sciences, Winthrop University, Rock Hill, SC, 29733, United States.

出版信息

Biochem Biophys Res Commun. 2021 Jul 5;561:93-100. doi: 10.1016/j.bbrc.2021.05.029. Epub 2021 May 18.

Abstract

AKT1 plays a key role in cell growth and survival, and its activation in cancers is mediated by different mechanisms. In this study, we investigated the potential of G-quadruplex (G4) formation by multiple consecutive G-tracts in the AKT1 promoter and its 3'-UTR. In circular dichroism analyses, synthetic oligonucleotides based on these G-tract regions showed molar ellipticity peaks at specific wavelengths of G4 structures. We verified G4 forming potential of these oligonucleotides using dimethyl sulfate footprinting, gel-shift and immunostaining assays. In reporter assays, mutations of the G-tracts in either the promoter or the 3'-UTR of AKT1 reduced expression mediated by these G-rich regions, suggesting positive regulation of AKT1 gene expression by these G4 structures. Furthermore, SP1 bound to its consensus sites regardless of the presence of G4 motifs in the AKT1 promoter, and both the G4 motifs and SP1 binding sites were needed to reach the strongest promoter strength.

摘要

AKT1 在细胞生长和存活中发挥关键作用,其在癌症中的激活是由不同的机制介导的。在这项研究中,我们研究了 AKT1 启动子及其 3'UTR 中多个连续 G tract 形成 G-四链体 (G4) 的潜力。在圆二色性分析中,基于这些 G-tract 区域的合成寡核苷酸在 G4 结构的特定波长处显示出摩尔椭圆度峰。我们使用硫酸二甲酯足迹、凝胶迁移和免疫染色测定验证了这些寡核苷酸形成 G4 的潜力。在报告基因实验中,AKT1 启动子或 3'UTR 中 G-tract 的突变降低了这些富含 G 的区域介导的表达,这表明这些 G4 结构对 AKT1 基因表达的正向调节。此外,SP1 结合其共有位点,无论 AKT1 启动子中是否存在 G4 基序,并且 G4 基序和 SP1 结合位点都需要达到最强的启动子强度。

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