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探索 c-Myb 基因中的 G-四链体功能及其拓扑替康的转录调控作用。

Exploration of G-quadruplex function in c-Myb gene and its transcriptional regulation by topotecan.

机构信息

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Department of Chemical Biology, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, China.

Institute of Vascular Medicine, Department of Cardiology, Peking University Third Hospital, Key Laboratory of Molecular Cardiovascular Sciences of Ministry of Education, Key Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides, Ministry of Health, Beijing, 100191, China.

出版信息

Int J Biol Macromol. 2018 Feb;107(Pt B):1474-1479. doi: 10.1016/j.ijbiomac.2017.10.010. Epub 2017 Oct 5.

Abstract

Our bioinformatics research shows that there are four G-rich sequences (S1-S4) in the upstream region of the transcription start site of c-Myb gene, and we have proved that these sequences have the ability to form G-quadruplex structures. This work mainly focuses on G-quadruplex function, recognition and transcription regulation in c-Myb gene, revealing a novel regulatory element in c-Myb proximal promoter region, and its transcription regulation by G-quadruplex binder. The research has identified that the enhancer effect in c-Myb transcription was primarily affected by the G-quadruplex formed by S1 sequence, and the up-regulation effect may due to the removal of repressive progress of MZF-1 by stabilizing G-quadruplex. Attentions were being paid to the development of G-quadruplex binders for selective recognition, and topotecan was found to have high binding affinity in vitro and could effectively affect the c-Myb transcription activities in cells. The regulation of G-quadruplex with binders in transcriptional, translational levels by Q-RT-PCR and western blot was in expectation of providing a strategy for gene expression modulation. In conclusion, our study revealed a G-quadruplex structure in c-Myb proximal promoter region, which was of great importance in the regulation of c-Myb function.

摘要

我们的生物信息学研究表明,c-Myb 基因转录起始位点上游区域存在四个富含 G 的序列(S1-S4),我们已经证明这些序列具有形成 G-四链体结构的能力。这项工作主要集中在 c-Myb 基因中的 G-四链体功能、识别和转录调控,揭示了 c-Myb 近端启动子区域的一个新的调控元件及其通过 G-四链体结合物的转录调控。研究表明,c-Myb 转录中的增强子效应主要受 S1 序列形成的 G-四链体影响,而上调效应可能是由于通过稳定 G-四链体,去除了 MZF-1 的抑制作用。人们关注 G-四链体结合物的选择性识别的发展,发现拓扑替康在体外具有高结合亲和力,并能有效影响细胞中的 c-Myb 转录活性。通过 Q-RT-PCR 和 Western blot 在转录和翻译水平上对 G-四链体的调节,有望为基因表达调控提供一种策略。总之,我们的研究揭示了 c-Myb 近端启动子区域的 G-四链体结构,这对 c-Myb 功能的调节具有重要意义。

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