PyV genomes typically encode and express two regulatory proteins, the small tumor and large tumor antigens, during early infection (early gene proteins). Three capsid proteins, VP1, VP2, VP3, are expressed after the beginning of viral DNA replication (late gene proteins). The genome maps identify known Open Reading Frames (ORFs) and include annotated viral proteins.
Major capsid protein of polyomavirus; 72 pentamers of VP1 comprise the outer capsid and form a T = 7 icosahedral lattice; VP1 contains an amino-terminal bipartite nuclear targeting signal that overlaps its DNA-binding-domain; The polyomaviruses are non-enveloped dsDNA viruses with a major capsid protein, VP1, that facilitates binding of genomic DNA and entry into target cells; the viral genome is organized into two divergent transcriptional units known as early and late regions; mRNAs from the early region encode the viral small and large t-antigens; mRNAs from the late region encode the structural proteins, VP1, VP2 and VP3
Promotes the efficient replication of genomic DNA; binds to and negatively regulates the function of protein phosphotase (PP2A) thereby accelerating the progression to S-phase; the small T antigen is not essential for replication in all cell lines
Binds to the viral origin of replication; regulates the transcription of early region mRNA; helicase activity facilitates movement of the virion DNA replication fork; the small T antigen shares a region in common with the large T antigen known as the J-domain; the J-domain is required for multiple processes including assembly, viral genomic DNA replication and transcription; The polyomaviruses are non-enveloped dsDNA viruses; the viral genome is organized into two divergent transcriptional units known as early and late regions; mRNAs from the early region encode the viral small and large t-antigens; the small T antigen and large T antigen are expressed upon entry into the host nucleus early in the viral lifecycle