tetano
Editor, Senior Moderator
Sci Rep
. 2023 Apr 29;13(1):7042.
doi: 10.1038/s41598-023-34285-7. Phosphorylation of the PA subunit of influenza polymerase at Y393 prevents binding of the 5'-termini of RNA and polymerase function
Lu Liu[SUP] 1 2 [/SUP], Ramakanth Madhugiri[SUP] 2 [/SUP], Vera Vivian Saul[SUP] 1 [/SUP], Susanne Bacher[SUP] 1 [/SUP], Michael Kracht[SUP] 3 [/SUP], Stephan Pleschka[SUP] 2 4 [/SUP], M Lienhard Schmitz[SUP] 5 [/SUP]
Affiliations
The 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.
. 2023 Apr 29;13(1):7042.
doi: 10.1038/s41598-023-34285-7. Phosphorylation of the PA subunit of influenza polymerase at Y393 prevents binding of the 5'-termini of RNA and polymerase function
Lu Liu[SUP] 1 2 [/SUP], Ramakanth Madhugiri[SUP] 2 [/SUP], Vera Vivian Saul[SUP] 1 [/SUP], Susanne Bacher[SUP] 1 [/SUP], Michael Kracht[SUP] 3 [/SUP], Stephan Pleschka[SUP] 2 4 [/SUP], M Lienhard Schmitz[SUP] 5 [/SUP]
Affiliations
- PMID: 37120635
- PMCID: PMC10148841
- DOI: 10.1038/s41598-023-34285-7
The 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.