Protein Synthesis Shut-Off Induced by Influenza Virus Infection Is Independent of PKR Activity

Author:

Zürcher Thomas1,Marión Rosa María1,Ortín Juan1

Affiliation:

1. Centro Nacional de Biotecnologı́a (CSIC), Campus de Cantoblanco, 28049 Madrid, Spain

Abstract

ABSTRACT The role of PKR activity in influenza virus-induced cell shut-off was studied by infection of PKR + or PKR cell cultures and metabolic labeling in vivo. No differences in the synthesis of viral proteins or the decay of cellular protein synthesis were observed. To investigate the relevance of the inhibition of cellular pre-mRNA polyadenylation and nucleocytoplasmic transport in virus-induced shut-off, we carried out similar experiments with mutant viruses lacking C-terminal sequences of NS1 protein. No differences in the shut-off induced by mutant versus wild-type viruses were observed, indicating that these nuclear events are not relevant for shut-off. The analysis of cytoplasmic mRNA stability indicated that the accumulation of viral mRNA during the infection correlated with the progressive decay of cellular mRNA, in both the wild type and an NS1 deletion mutant.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference28 articles.

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2. Degradation of cellular mRNA during influenza virus infection: its possible role in protein synthesis shutoff;Beloso A.;J. Gen. Virol.,1992

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4. Influenza A virus NS1 protein targets poly(A)-binding protein II of the cellular 3'-end processing machinery

5. The double-stranded RNA-dependent protein kinase PKR: structure and function;Clemens M. J.;J. Interferon Cytokine Res.,1997

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