JNK kinase regulates phosphorylation of HCoV-229E nucleocapsid protein

Identifying common host factors essential for the replication cycles of human coronaviruses (HCoV) could help uncover potential therapeutic targets. Mitogen-activated protein kinases (MAPKs) regulate critical cellular signaling pathways. Among them, c-Jun N-terminal kinases (JNK) are activated in response to diverse environmental stresses, including viral infections. However, the relevance of the JNK pathway for host responses and replication of HCoV infections has remained elusive. Using live-cell microscopy, quantitative immunofluorescence and immunoblotting, we found that JNK is specifically activated in cells infected with HCoV-229E and plays a crucial role in mediating the phosphorylation of the viral nucleocapsid (N) protein, an essential step required during the viral replication cycle. Consequently, pharmacological inhibition of JNK kinase activity impeded HCoV-229E as well as SARS-CoV-2 infection. Given the conservation of phosphorylation sites within the nucleocapsid protein across coronaviruses, inhibitors targeting these N protein kinases, such as JNK, may hold therapeutic promise as broad-spectrum CoV antivirals.

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Publication Details

Journal
npj Viruses
Published
2025-09-18
DOI
https://doi.org/10.1038/s44298-025-00152-7
Citations
4
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
5.58

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article

JNK kinase regulates phosphorylation of HCoV-229E nucleocapsid protein

Yannick Brüggemann, Maximilian K. Nocke, Toni Luise Meister, Daniel Tödt et al.
4 citations
npj Viruses
SARS-CoV-2 and COVID-19 Research
5.58
article

JNK kinase regulates phosphorylation of HCoV-229E nucleocapsid protein

Yannick Brüggemann, Maximilian K. Nocke, Toni Luise Meister, Daniel Tödt, Natalie Heinen, Eike Steinmann, Michael Poppe, Michael Kracht, Stephanie Pfaender, Elizabeth R. Richter, Saskia Westhoven, Mohammed Samer Shaban, Leyla Sirkinti
article en
4 citations

Abstract

Identifying common host factors essential for the replication cycles of human coronaviruses (HCoV) could help uncover potential therapeutic targets. Mitogen-activated protein kinases (MAPKs) regulate critical cellular signaling pathways. Among them, c-Jun N-terminal kinases (JNK) are activated in response to diverse environmental stresses, including viral infections. However, the relevance of the JNK pathway for host responses and replication of HCoV infections has remained elusive. Using live-cell microscopy, quantitative immunofluorescence and immunoblotting, we found that JNK is specifically activated in cells infected with HCoV-229E and plays a crucial role in mediating the phosphorylation of the viral nucleocapsid (N) protein, an essential step required during the viral replication cycle. Consequently, pharmacological inhibition of JNK kinase activity impeded HCoV-229E as well as SARS-CoV-2 infection. Given the conservation of phosphorylation sites within the nucleocapsid protein across coronaviruses, inhibitors targeting these N protein kinases, such as JNK, may hold therapeutic promise as broad-spectrum CoV antivirals.

npj VirusesVol. 3(1)
Universität Hamburg (DE), Justus-Liebig-Universität Gießen (DE), University Medical Center Hamburg-Eppendorf (DE), German Center for Infection Research (DE), Ruhr University Bochum (DE), University of Lübeck (DE), Bernhard Nocht Institute for Tropical Medicine (DE)
Deutsches Zentrum für Infektionsforschung, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung
Openalex Percentile: Top 4%
SARS-CoV-2 and COVID-19 Research
5.58
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