The mechanism of RNA capping by SARS-CoV-2

Article

关键词: CRYO-EM STRUCTURE;    VESICULAR STOMATITIS-VIRUS;    MESSENGER-RNA;    PROTEIN;    TRANSCRIPTION;    POLYMERASE;    REPLICATION;    METHYLATION;    5'-TERMINUS;    FEATURES;   

DOI  :  10.1038/s41586-022-05185-z

来源: SCIE

【 摘 要 】

The RNA genome of SARS-CoV-2 contains a 5' cap that facilitates the translation of viral proteins, protection from exonucleases and evasion of the host immune response(1-4). How this cap is made in SARS-CoV-2 is not completely understood. Here we reconstitute the N7- and 2'-O-methylated SARS-CoV-2 RNA cap ((7Me)GpppA(2'- O-Me)) using virally encoded non-structural proteins (nsps). We show that the kinase-like nidovirus RdRp-associated nucleotidyltransferase (NiRAN) domain(5) of nsp12 transfers the RNA to the amino terminus of nsp9, forming a covalent RNA-protein intermediate (a process termed RNAylation). Subsequently, the NiRAN domain transfers the RNA to GDP, forming the core cap structure GpppA-RNA. The nsp14(6) and nsp16(7) methyltransferases then add methyl groups to form functional cap structures. Structural analyses of the replication-transcription complex bound to nsp9 identified key interactions that mediate the capping reaction. Furthermore, we demonstrate in a reverse genetics system(8) that the N terminus of nsp9 and the kinase-like active-site residues in the NiRAN domain are required for successful SARS-CoV-2 replication. Collectively, our results reveal an unconventional mechanism by which SARS-CoV-2 caps its RNA genome, thus exposing a new target in the development of antivirals to treat COVID-19.

【 授权许可】

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