Proceedings of the National Academy of Sciences · 1984 · 47 citations · 27 references
Life SciencesMicrobiologyMolecular BiologyCancer ImmunologyMolecular VirologyVirologyAntiviral ImmunityOncogenic VirusesViral InfectionsDeletion MutationsEpstein-barr Virus LatencyEpstein-barr Virus PersistenceImmunofluorescence AssaysIndirect Immunofluorescence AssayRestriction Endonuclease SpecificityViral Antigen RecognitionViral Expression Vectors
The Epstein-Barr virus (EBV) BamHI restriction endonuclease fragment K (B95-8 strain) was introduced into a polyoma virus expression vector and used to transfect murine NIH 3T3 cells. An EBV-associated nuclear antigen was detected in these cells in an indirect immunofluorescence test using anti-EBV nuclear antigen-positive human sera. These sera recognized a Mr 88,000 polypeptide in 3T3 cells transfected with the BamHI fragment K-containing polyoma virus plasmid by radioimmunoelectrophoresis. A Mr 88,000 polypeptide also was detected in a B-cell line latently infected with the B95-8 strain of EBV. Plasmids containing insertion and deletion mutations in BamHI fragment K directed the synthesis of truncated forms of the Mr 88,000 polypeptide in 3T3 cells. These data directly demonstrate that the polypeptide identified in EBV-infected lymphocyte lines by anti-EBV nuclear antigen-positive human sera is encoded by the viral genome.
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
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