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Biomolecular Condensation of the Human Papillomavirus E2 Master Regulator with p53: Implications in Viral Replication

Susana Borkosky, Silvia; Fassolari, Marisol; Campos-León, Karen; Hugo Rossi, Andrés; Salgueiro, Mariano; Antonela Pascuale, Carla; Peralta Martínez, Ramón; Gaston, Kevin; de Prat Gay, Gonzalo

Authors

Silvia Susana Borkosky

Marisol Fassolari

Karen Campos-León

Andrés Hugo Rossi

Mariano Salgueiro

Carla Antonela Pascuale

Ramón Peralta Martínez

Gonzalo de Prat Gay



Abstract

p53 exerts its tumour suppressor activity by modulating hundreds of genes and it can also repress viral replication. Such is the case of human papillomavirus (HPV) through targeting the E2 master regulator, but the biochemical mechanism is not known. We show that the C-terminal DNA binding domain of HPV16 E2 protein (E2C) triggers heterotypic condensation with p53 at a precise 2/1 E2C/p53 stoichiometry at the onset for demixing, yielding large regular spherical droplets that increase in size with E2C concentration. Interestingly, transfection experiments show that E2 co-localizes with p53 in the nucleus with a grainy pattern, and recruits p53 to chromatin-associated foci, a function independent of the DNA binding capacity of p53 as judged by a DNA binding impaired mutant. Depending on the length, DNA can either completely dissolve or reshape heterotypic droplets into irregular condensates containing p53, E2C, and DNA, and reminiscent of that observed linked to chromatin. We propose that p53 is a scaffold for condensation in line with its structural and functional features, in particular as a promiscuous hub that binds multiple cellular proteins. E2 appears as both client and modulator, likely based on its homodimeric DNA binding nature. Our results, in line with the known role of condensation in eukaryotic gene enhancement and silencing, point at biomolecular condensation of E2 with p53 as a means to modulate HPV gene function, strictly dependent on host cell replication and transcription machinery.

Journal Article Type Article
Acceptance Date Nov 7, 2022
Online Publication Date Nov 17, 2022
Publication Date Nov 17, 2022
Deposit Date Jan 24, 2023
Publicly Available Date Nov 18, 2023
Journal Journal of Molecular Biology
Electronic ISSN 1089-8638
Peer Reviewed Peer Reviewed
Article Number 167889
DOI https://doi.org/10.1016/j.jmb.2022.167889
Keywords p53, Viral protein, Human papillomavirus, LLPS, E2 DNA binding domain
Public URL https://nottingham-repository.worktribe.com/output/14587983
Publisher URL https://www.sciencedirect.com/science/article/abs/pii/S0022283622005095?via%3Dihub

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