TY - JOUR
T1 - G-quadruplexes are promoter elements controlling nucleosome exclusion and RNA polymerase II pausing
AU - Esnault, Cyril
AU - Zine El Aabidine, Amal
AU - Robert, Marie Cécile
AU - Cucchiarini, Anne
AU - Magat, Talha
AU - Pigeot, Alexia
AU - Bouchouika, Soumya
AU - Garcia-Oliver, Encar
AU - Gawron, Kevin
AU - Basyuk, Eugénia
AU - Karpinska, Magdalena A.
AU - Kozulic-Pirher, Alja
AU - Luo, Yu
AU - Verga, Daniela
AU - Mourad, Raphael
AU - Radulescu, Ovidiu
AU - Mergny, Jean Louis
AU - Bertrand, Edouard
AU - Andrau, Jean Christophe
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature America, Inc. 2025.
PY - 2025/8/1
Y1 - 2025/8/1
N2 - Despite their central role in transcription, it has been difficult to define universal sequences associated with eukaryotic promoters. Within the chromatin context, recruitment of transcriptional machinery requires promoter opening, but how DNA elements contribute to this process is unclear. Here we show that G-quadruplex (G4) secondary DNA structures are highly enriched at mammalian promoters. 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 in vivo and in vitro while favouring strong positioning. At model promoters, impairing G4s affected both transcriptional activity and chromatin opening. G4 destabilization also resulted in an inactive promoter state and affected the transition to effective RNA production. 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 RNA polymerase II.
AB - Despite their central role in transcription, it has been difficult to define universal sequences associated with eukaryotic promoters. Within the chromatin context, recruitment of transcriptional machinery requires promoter opening, but how DNA elements contribute to this process is unclear. Here we show that G-quadruplex (G4) secondary DNA structures are highly enriched at mammalian promoters. 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 in vivo and in vitro while favouring strong positioning. At model promoters, impairing G4s affected both transcriptional activity and chromatin opening. G4 destabilization also resulted in an inactive promoter state and affected the transition to effective RNA production. 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 RNA polymerase II.
UR - https://www.scopus.com/pages/publications/105011208440
U2 - 10.1038/s41588-025-02263-6
DO - 10.1038/s41588-025-02263-6
M3 - Article
AN - SCOPUS:105011208440
SN - 1061-4036
VL - 57
SP - 1981
EP - 1993
JO - Nature Genetics
JF - Nature Genetics
IS - 8
ER -