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Existence of G-quadruplex structures in promoter region of oncogenes confirmed by G-quadruplex DNA cross-linking strategy

机译:G四联体DNA交联策略证实致癌基因启动子区域中G四联体结构的存在

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摘要

Existence of G-quadruplex DNA in vivo always attract widespread interest in the field of biology and biological chemistry. We reported our findings for the existence of G-quadruplex structures in promoter region of oncogenes confirmed by G-quadruplex DNA cross-linking strategy. Probes for selective G-quadruplex cross-linking was designed and synthesized that show high selectivity for G-quadruplex cross-linking. Further biological studies demonstrated its good inhibition activity against murine melanoma cells. To further investigate if G-quadruplex DNA was formed in vivo and as the target, a derivative was synthesized and pull-down process toward chromosome DNAs combined with circular dichroism and high throughput deep sequencing were performed. Several simulated intracellular conditions, including X. laevis oocytes, Ficoll 70 and PEG, was used to investigate the compound's pure cross-linking ability upon preformed G-quadruplex. Thus, as a potent G-quadruplex cross-linking agent, our strategy provided both valuable evidence of G-quadruplex structures in vivo and intense potential in anti-cancer therapy.
机译:体内G-四链体DNA的存在一直引起生物学和生物化学领域的广泛兴趣。我们报告了我们的发现,通过G-四链体DNA交联策略证实了癌基因启动子区域中G-四链体结构的存在。设计并合成了选择性G-四链体交联探针,这些探针对G-四链体交联具有高选择性。进一步的生物学研究表明其对鼠类黑色素瘤细胞具有良好的抑制活性。为了进一步研究是否在体内形成G-四链体DNA并以其为靶标,合成了一种衍生物,并结合了圆二色性和高通量深度测序进行了向染色体DNA的下拉过程。几种模拟的细胞内条件,包括X. laevis卵母细胞,Ficoll 70和PEG,用于研究该化合物在预先形成的G-四链体上的纯交联能力。因此,作为有效的G-四链体交联剂,我们的策略既提供了体内G-四链体结构的有价值证据,又提供了抗癌治疗的强大潜力。

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