The N-terminal half of the influenza virus NS1 protein is sufficient for nuclear retention of mRNA and enhancement of viral mRNA translation
- PMID: 9336457
- PMCID: PMC147036
- DOI: 10.1093/nar/25.21.4271
The N-terminal half of the influenza virus NS1 protein is sufficient for nuclear retention of mRNA and enhancement of viral mRNA translation
Abstract
A collection of C-terminal deletion mutants of the influenza A virus NS1 gene has been used to define the regions of the NS1 protein involved in its functionality. Immunofluorescence analyses showed that the NS1 protein sequences downstream from position 81 are not required for nuclear transport. The capacity of these mutants to bind RNA was studied by in vitro binding tests using a model vRNA probe. These experiments showed that the N-terminal 81 amino acids of NS1 protein are sufficient for RNA binding activity. The collection of mutants also served to map the NS1 sequences required for nuclear retention of mRNA and for stimulation of viral mRNA translation, using the NP gene as reporter. The results obtained indicated that the N-terminal 113 amino acids of NS1 protein are sufficient for nuclear retention of mRNA and stimulation of viral mRNA translation. The possibility that this region of the protein may be sufficient for virus viability is discussed in relation to the sequences of NS1 genes of field isolates and to the phenotype of known viral mutants affected in the NS1 gene.
Similar articles
-
Mutation analysis of a recombinant NS replicon shows that influenza virus NS1 protein blocks the splicing and nucleo-cytoplasmic transport of its own viral mRNA.Nucleic Acids Res. 2007;35(14):4573-82. doi: 10.1093/nar/gkm230. Epub 2007 May 8. Nucleic Acids Res. 2007. PMID: 17488845 Free PMC article.
-
Characterization of influenza virus NS1 protein by using a novel helper-virus-free reverse genetic system.J Virol. 2000 Jun;74(12):5556-61. doi: 10.1128/jvi.74.12.5556-5561.2000. J Virol. 2000. PMID: 10823862 Free PMC article.
-
The NS1 Protein from Influenza Virus Stimulates Translation Initiation by Enhancing Ribosome Recruitment to mRNAs.J Mol Biol. 2017 Oct 27;429(21):3334-3352. doi: 10.1016/j.jmb.2017.04.007. Epub 2017 Apr 20. J Mol Biol. 2017. PMID: 28433538
-
Nuclear functions of the influenza A and B viruses NS1 proteins: do they play a role in viral mRNA export?Vaccine. 2009 Oct 23;27(45):6312-6. doi: 10.1016/j.vaccine.2009.01.015. Vaccine. 2009. PMID: 19840666 Review.
-
Selective nuclear export of viral mRNAs in influenza-virus-infected cells.Trends Microbiol. 2000 Aug;8(8):376-83. doi: 10.1016/s0966-842x(00)01794-7. Trends Microbiol. 2000. PMID: 10920397 Review.
Cited by
-
Genetic analysis of influenza virus NS1 gene: a temperature-sensitive mutant shows defective formation of virus particles.J Virol. 2005 Dec;79(24):15246-57. doi: 10.1128/JVI.79.24.15246-15257.2005. J Virol. 2005. PMID: 16306596 Free PMC article.
-
Mutation analysis of a recombinant NS replicon shows that influenza virus NS1 protein blocks the splicing and nucleo-cytoplasmic transport of its own viral mRNA.Nucleic Acids Res. 2007;35(14):4573-82. doi: 10.1093/nar/gkm230. Epub 2007 May 8. Nucleic Acids Res. 2007. PMID: 17488845 Free PMC article.
-
The influenza A virus NS1 protein interacts with the nucleoprotein of viral ribonucleoprotein complexes.J Virol. 2011 May;85(10):5228-31. doi: 10.1128/JVI.02562-10. Epub 2011 Mar 16. J Virol. 2011. PMID: 21411538 Free PMC article.
-
Conserved and host-specific features of influenza virion architecture.Nat Commun. 2014 Sep 16;5:4816. doi: 10.1038/ncomms5816. Nat Commun. 2014. PMID: 25226414 Free PMC article.
-
New substitutions on NS1 protein from influenza A (H1N1) virus: Bioinformatics analyses of Indian strains isolated from 2009 to 2020.Health Sci Rep. 2022 Apr 25;5(3):e626. doi: 10.1002/hsr2.626. eCollection 2022 May. Health Sci Rep. 2022. PMID: 35509388 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous