| Abstract: |
The te16 mutation of vaccinia virus WR (R. C. Condit, A. Motyczka, and G. Spizz, Virology 128:429-443, 1983) has been mapped by marker rescue to the I7L open reading frame located within the genomic HindIII I DNA fragment. The 17 gene encodes a 423-amino-acid polypeptide. Thermolabile growth was attributed to an amino acid substitution, Pro-344→Leu, in the predicted 17 protein. A normal temporal pattern of viral protein synthesis was elicited in cells infected with ts16 at the nonpermissive temperature (40°C). Electron microscopy revealed a defect in virion assembly at 40°C. Morphogenesis was arrested at a stage subsequent to formation of spherical immature particles. Western immunoblot analysis with antiserum directed against the 17 polypeptide demonstrated an immunoreactive 47-kDa polypeptide accumulating during the late phase of synchronous vaccinia virus infection. Immunoblotting of extracts of wild-type virions showed that the 17 protein is encapsidated within the virus core. The 17 polypeptide displays amino acid sequence similarity to the type II DNA topoisomerase of Saccharomyces cerevisiae. |
| Keywords: |
controlled study; sequence analysis; mutation; core protein; comparative study; amino acid substitution; morphogenesis; immunoreactivity; amino acid sequence; molecular sequence data; sequence homology, amino acid; protein synthesis; immunoblotting; vaccinia virus; sequence homology; dna topoisomerase (atp hydrolysing); virus morphology; dna topoisomerases, type ii; virus protein; virus mutation; virion; temperature sensitive mutant; genes, viral; virus morphogenesis; priority journal; article; support, non-u.s. gov't; support, u.s. gov't, p.h.s.; viral core proteins
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