发起人
核小体
染色质
抄写(语言学)
RNA聚合酶Ⅱ
生物
RNA聚合酶
遗传学
核糖核酸
DNA
背景(考古学)
细胞生物学
基因
基因表达
哲学
古生物学
语言学
作者
Cyril Esnault,Encar García-Oliver,Amal Zine El Aabidine,Marie-Cécile Robert,Talha Magat,Kevin Gawron,Eugénia Basyuk,Magda Karpinska,Alexia Pigeot,Anne Cucchiarini,Yu Luo,Daniele Verga,Raphaël Mourad,Ovidiu Radulescu,Jean‐Louis Mergny,Édouard Bertrand,Jean‐Christophe Andrau
标识
DOI:10.1101/2023.02.24.529838
摘要
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.
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