Author:
Liu Lu,Madhugiri Ramakanth,Saul Vera Vivian,Bacher Susanne,Kracht Michael,Pleschka Stephan,Schmitz M. Lienhard
Abstract
AbstractThe influenza A virus (IAV) polymerase is a multifunctional machine that can adopt alternative configurations to perform transcription and replication of the viral RNA genome in a temporally ordered manner. Although the structure of polymerase is well understood, our knowledge of its regulation by phosphorylation is still incomplete. The heterotrimeric polymerase can be regulated by posttranslational modifications, but the endogenously occurring phosphorylations at the PA and PB2 subunits of the IAV polymerase have not been studied. Mutation of phosphosites in PB2 and PA subunits revealed that PA mutants resembling constitutive phosphorylation have a partial (S395) or complete (Y393) defect in the ability to synthesize mRNA and cRNA. As PA phosphorylation at Y393 prevents binding of the 5′ promoter of the genomic RNA, recombinant viruses harboring such a mutation could not be rescued. These data show the functional relevance of PA phosphorylations to control the activity of viral polymerase during the influenza infectious cycle.
Funder
Deutsche Forschungsgemeinschaft
Deutsches Zentrum für Infektionsforschung
Justus-Liebig-Universität Gießen
Publisher
Springer Science and Business Media LLC
Cited by
3 articles.
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