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Structural Basis for Influenza Virus NS1 Protein Block of mRNA Nuclear Export

Influenza viruses antagonize key immune defense mechanisms via the virulence factor NS1 protein. A major NS1 strategy is to block nuclear export of host mRNAs including those encoding immune factors(1–3); however, the direct cellular target of NS1 and the mechanism of host mRNA export inhibition are...

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Detalles Bibliográficos
Autores principales: Zhang, Ke, Xie, Yihu, Muñoz-Moreno, Raquel, Wang, Juan, Zhang, Liang, Esparza, Matthew, García-Sastre, Adolfo, Fontoura, Beatriz M.A., Ren, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754785/
https://www.ncbi.nlm.nih.gov/pubmed/31263181
http://dx.doi.org/10.1038/s41564-019-0482-x
Descripción
Sumario:Influenza viruses antagonize key immune defense mechanisms via the virulence factor NS1 protein. A major NS1 strategy is to block nuclear export of host mRNAs including those encoding immune factors(1–3); however, the direct cellular target of NS1 and the mechanism of host mRNA export inhibition are not known. Here, we identify the target of NS1 as the mRNA export receptor NXF1•NXT1, which is the principal receptor to mediate docking and translocation of mRNAs through the nuclear pore complex by interacting with nucleoporins(4,5). We determined the crystal structure of NS1 in complex with NXF1•NXT1 at 3.8 Å resolution. The structure reveals that NS1 prevents binding of NXF1•NXT1 to nucleoporins, thereby inhibiting mRNA export through the nuclear pore complex into the cytoplasm for translation. We demonstrate that a mutant influenza virus deficient in binding NXF1•NXT1 does not block host mRNA export and is attenuated. This attenuation is marked by the release of mRNAs encoding immune factors from the nucleus. Together, our study uncovers the molecular basis of a major nuclear function of influenza NS1 protein that causes potent blockage of host gene expression and contributes to inhibition of host immunity.