bioRxivMolecular BiologyPreprint
The strength of a NES motif in the nucleocapsid protein of human coronaviruses is related to genus, but not to pathogenic capacity
Maria SendinoiD, Miren Josu Omaetxebarria IbarraiD, José Antonio RodrígueziD
Abstract
Seven members of the Coronaviridae family infect humans, but only three (SARS-CoV, SARS-CoV-2 and MERS-CoV) cause severe disease with a high case fatality rate. Using in silico analyses (machine learning techniques and comparative genomics), several features associated to coronavirus pathogenicity have been recently proposed, including a potential increase in the strength of a predicted novel nuclear export signal (NES) motif in the nucleocapsid protein. Here, we have used a well-established nuclear export assay to experimentally establish whether the recently proposed nucleocapsid NESs are capable of mediating nuclear export, and to evaluate if their activity correlates with coronavirus pathogenicity. The six NES motifs tested were functional in our assay, but displayed wide differences in export activity. Importantly, these differences in NES strength were not related to strain pathogenicity. Rather, we found that the NESs of the strains belonging to the genus Alphacoronavirus were markedly stronger than the NESs of the strains belonging to the genus Betacoronavirus. We conclude that, while some of the genomic features recently identified in silico could be crucial contributors to coronavirus pathogenicity, this does not appear to be the case of nucleocapsid NES activity, as it is more closely related to coronavirus genus than to pathogenic capacity.
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Genomic determinants of pathogenicity in SARS-CoV-2 and other human coronaviruses
N. Auslander, A. B. Gussow, … E. V. Koonin·bioRxiv·Apr 5, 2020
- Coronavirus nucleocapsid proteins differentially antagonize RIG-I-like receptor signaling to shape pathogenicity
Yajuan Rui, Yanpu Wang, … Xiao-Fang Yu·bioRxiv·Oct 10, 2026
- Characterising alphacoronavirus phenotypic traits through diversity-driven selection of spike
Giulia Gallo, Antonello Di Nardo, … Dalan Bailey·bioRxiv·Nov 22, 2024
- The coronavirus nsp14 exoribonuclease interface with the cofactor nsp10 is essential for efficient virus replication and enzymatic activity.
Samantha L. Grimes, Brook E. Heaton, … Jordan Anderson-Daniels·Journal of VirologyPeer-reviewed·Jan 10, 2025
- Loss of nsp14-exonuclease activity impairs the replication, proofreading, fitness and pathogenesis of SARS-CoV-2
Jordan Anderson-Daniels, Meghan V. Diefenbacher, … Timothy Patrick Sheahan·mBioPeer-reviewed·May 6, 2026
- Mutations in SARS-CoV-2 Nsp1 are critical determinants of viral pathogenicity in mice
Nathaniel D. Jackson, Fuchun Zhou, … Luis Martínez‐Sobrido·bioRxiv·Aug 19, 2026