| Literature DB >> 28219018 |
Chutikarn Chaimayo1, Tsuyoshi Hayashi2, Andrew Underwood2, Erin Hodges2, Toru Takimoto3.
Abstract
Influenza A viruses contain eight single-stranded, negative-sense RNA segments as viral genomes in the form of viral ribonucleoproteins (vRNPs). During genome replication in the nucleus, positive-sense complementary RNPs (cRNPs) are produced as replicative intermediates, which are not incorporated into progeny virions. To analyze the mechanism of selective vRNP incorporation into progeny virions, we quantified vRNPs and cRNPs in the nuclear and cytosolic fractions of infected cells, using a strand-specific qRT-PCR. Unexpectedly, we found that cRNPs were also exported to the cytoplasm. This export was chromosome region maintenance 1 (CRM1)-independent unlike that of vRNPs. Although both vRNPs and cRNPs were present in the cytosol, viral matrix (M1) protein, a key regulator for viral assembly, preferentially bound vRNPs over cRNPs. These results indicate that influenza A viruses selectively uptake cytosolic vRNPs through a specific interaction with M1 during viral assembly.Entities:
Keywords: Assembly; CRM1; CRNP; Influenza; M1; Nuclear export; Trafficking; VRNP
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Year: 2017 PMID: 28219018 PMCID: PMC5366082 DOI: 10.1016/j.virol.2017.02.008
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616