Regulation of respiratory syncytial virus nucleoprotein oligomerization by phosphorylation

The negative-sense RNA genome of respiratory syncytial virus (RSV) is encapsidated by the viral nucleoprotein N, forming a left-handed helical nucleocapsid which serves as template for the viral polymerase. Specific oligomerization of N along the viral genome necessitates a switch of conformation of N, from the neosynthesized monomeric and RNA-free N protein, named N<sup>0</sup>, to N-RNA oligomers. Although the binding of the N-terminal part of RSV phosphoprotein P plays the role of chaperone to impair RNA binding to N, N<sup>0</sup>-P interaction alone is not sufficient to prevent N oligomerization. Here, we explored the potential role of post translational modifications that could participate in the stability of N<sup>0</sup>. Among the post translational modifications specifically identified on recombinant monomeric N, we validated the presence of a phosphorylation site on residue Y88 of N which modulates N oligomerization. Our results suggest that RSV N oligomerization depends on the regulation by post translational modifications.

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Publication Details

Journal
Journal of Biological Chemistry
Published
2025-02-03
DOI
https://doi.org/10.1016/j.jbc.2025.108256
Citations
6
Primary Topic
Respiratory viral infections research
Type
article
Field-Weighted Citation Impact
8.13

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article

Regulation of respiratory syncytial virus nucleoprotein oligomerization by phosphorylation

Charles-Adrien Richard, Marie Galloux, Cédric Leyrat, Vincent Basse et al.
6 citations
Journal of Biological Chemistry
Respiratory viral infections research
8.13
article

Regulation of respiratory syncytial virus nucleoprotein oligomerization by phosphorylation

Charles-Adrien Richard, Marie Galloux, Cédric Leyrat, Vincent Basse, Céline Henry, Yao Wang, Carine Rodrigues-Machado
article en
6 citations

Abstract

The negative-sense RNA genome of respiratory syncytial virus (RSV) is encapsidated by the viral nucleoprotein N, forming a left-handed helical nucleocapsid which serves as template for the viral polymerase. Specific oligomerization of N along the viral genome necessitates a switch of conformation of N, from the neosynthesized monomeric and RNA-free N protein, named N<sup>0</sup>, to N-RNA oligomers. Although the binding of the N-terminal part of RSV phosphoprotein P plays the role of chaperone to impair RNA binding to N, N<sup>0</sup>-P interaction alone is not sufficient to prevent N oligomerization. Here, we explored the potential role of post translational modifications that could participate in the stability of N<sup>0</sup>. Among the post translational modifications specifically identified on recombinant monomeric N, we validated the presence of a phosphorylation site on residue Y88 of N which modulates N oligomerization. Our results suggest that RSV N oligomerization depends on the regulation by post translational modifications.

Journal of Biological ChemistryVol. 301(3)
Centre National de la Recherche Scientifique (FR), Inserm (FR), Université de Montpellier (FR), AgroParisTech (FR), Université Paris-Saclay (FR), Microbiologie de l’alimentation au service de la santé (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), Virologie et Immunologie Moléculaires (FR), Institut de Génomique Fonctionnelle (FR)
Agence Nationale de la Recherche
Openalex Percentile: Top 3%
Respiratory viral infections research
8.13
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