G-quadruplexes are promoter elements controlling nucleosome exclusion and RNA polymerase II pausing

C. Esnault, Encar García-Oliver, Amal Zine El Aabidine, Marie-Cécile Robert, Talha Magat, Kevin Gawron, E. Basyuk, Magdalena A. Karpinska, Alexia Pigeot, Anne Cucchiarini, Yu Luo, Daniele Verga, R. Mourad, O. Radulescu, J. Mergny, E. Bertrand, J. Andrau
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引用次数: 1

Abstract

Despite their central role in transcription, it has been difficult to define universal sequences associated to eukaryotic promoters. Within chromatin context, recruitment of the transcriptional machinery requires opening of the promoter but how DNA elements could contribute to this process has remained elusive. Here, we show that G-quadruplex (G4) secondary structures are highly enriched mammalian core promoter elements. G4s are located at the deepest point of nucleosome exclusion at promoters and correlate with maximum promoter activity. We found that experimental G4s exclude nucleosomes both in vivo and in vitro and display a strong positioning potential. At model promoters, impairing G4s affected both transcriptional activity and chromatin opening. G4 destabilization also resulted in an inactive promoter state and affected transition to effective RNA production in live imaging experiments. Finally, G4 stabilization resulted in global reduction of proximal promoter pausing. Altogether, our data introduce G4s as bona fide promoter elements allowing nucleosome exclusion and facilitating pause release by the RNA Polymerase II.
g -四联体是控制核小体排斥和RNA聚合酶II暂停的启动子元件
尽管它们在转录中起着中心作用,但很难定义与真核生物启动子相关的普遍序列。在染色质背景下,转录机制的招募需要打开启动子,但DNA元件如何参与这一过程仍然是难以捉摸的。在这里,我们发现g -四重体(G4)二级结构是高度富集的哺乳动物核心启动子元件。G4s位于启动子核小体排斥的最深处,与最大启动子活性相关。我们发现实验G4s在体内和体外都排除核小体,并显示出很强的定位潜力。在模型启动子上,受损的G4s影响转录活性和染色质打开。在实时成像实验中,G4不稳定也导致启动子状态失活,影响向有效RNA生产的转变。最后,G4稳定导致近端启动子暂停的整体减少。总之,我们的数据介绍了G4s作为真正的启动子元件,允许核小体排斥和促进RNA聚合酶II的暂停释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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