1887

Abstract

SUMMARY

Using both selection enrichment and site-directed mutagenesis, a herpes simplex virus type 1 (HSV-1) strain 17 genome lacking all four I sites has been generated. The site at 0·45 map units which lies within the gene coding for a polypeptide of 28 000 molecular weight was removed by selection enrichment, while the site at 0·29 map units which lies within the gene coding for glycoprotein H was removed by site-directed mutagenesis. The parental virus from which these two I sites were deleted had previously had the sites at 0·07 and 0·63 map units removed through selection enrichment. The variant devoid of I sites (X4) showed normal growth characteristics; its phenotype was normal apart from the absence of the thymidine kinase protein, which is believed to be unrelated to the loss of I sites.

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1987-04-01
2024-05-08
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References

  1. Ben-Porat T., Brown L., Veach R. A. 1982; Recombination occurs mainly between parental genomes and precedes DNA replication in pseudorabies virus-infected cells. Journal of Virology 44:134–143
    [Google Scholar]
  2. Brown S. M., Ritchie D. A. 1975; Genetic studies of herpes simplex virus type 1. Analysis of mixed plaqueforming virus and its bearing on genetic recombination. Virology 64:32–42
    [Google Scholar]
  3. Brown S. M., Ritchie D. A., Surak-Sharpe J. H. 1973; Genetic studies with herpes simplex virus type 1. The isolation of temperature-sensitive mutants, their arrangement into complementation groups and recombination analysis leading to a linkage map. Journal of General Virology 18:329–346
    [Google Scholar]
  4. Brown S. M., Harland J., Subak-Sharpe J. H. 1984; Isolation of restriction endonuclease site deletion mutants of herpes simplex virus. Journal of General Virology 65:1053–1068
    [Google Scholar]
  5. Buckmaster E. A., Gompels V., Minson A. C. 1984; Characterization and physical mapping of an HSV-1 glycoprotein of approximately 115 × 103 molecular weight. Virology 139:408–413
    [Google Scholar]
  6. Cook S. D., Brown S. M. 1987; Herpes simplex virus type 1 latency in rabbit corneal cellsin vitro:reactivation and recombination following intratypic superinfection of long term cultures. Journal of General Virology 68:813–824
    [Google Scholar]
  7. Dargan D. J., Surak-Sharpe J. H. 1985; The effect of triterpenoid compounds on uninfected and herpes simplex virus-infected cells in culture. I. Effect on cell growth, virus particles and virus replication. Journal of General Virology 66:1771–1784
    [Google Scholar]
  8. Dasgupta U. B., Summers W. C. 1980; Genetic recombination of herpes simplex virus, the role of the host cell and UV-irradiation of the virus. Molecular and General Genetics 178:617–623
    [Google Scholar]
  9. Davison A. J., Wilkie N. M. 1981; Nucleotide sequences of the joint between the L and S segments of herpes simplex virus types 1 and 2. Journal of General Virology 55:315–331
    [Google Scholar]
  10. Harland J., Brown S. M. 1985; Isolation and characterization of deletion mutants of herpes simplex virus type 2 (strain HG52). Journal of General Virology 66:1305–1321
    [Google Scholar]
  11. Honess R. W., Buchan A., Halliburton I. W., Watson D. H. 1980; Recombination and linkage between structural and regulatory genes of herpes simplex virus type 1 : study of the functional organization of the genome. Journal of Virology 34:716–742
    [Google Scholar]
  12. Jones W., Shenk T. 1978; Isolation of deletion and substitution mutants of adenovirus 5. Cell 13:181–188
    [Google Scholar]
  13. Jones W., Shenk T. 1979; Isolation of adenovirus type 5 host range deletion mutants defective for transformation of rat embryo cells. Cell 17:683–689
    [Google Scholar]
  14. Liang S-M., Thatcher D. R., Liang C-M., Allet B. 1986; Studies of structure-activity relationships of human interleukin-2. Journal of Biological Chemistry 261:334–337
    [Google Scholar]
  15. Lonsdale D. I. 1979; A rapid technique for distinguishing herpes simplex virus type 1 from type 2 by restriction enzyme technology. Lancet i:849–852
    [Google Scholar]
  16. McGeoch D. J., Davison A. J. 1986; DNA sequence of the herpes simplex virus type 1 gene encoding glycoprotein gH, and identification of homologues in the genomes of varicella-zoster virus and Epstein-Barr virus. Nucleic Acids Research 14:4281–4292
    [Google Scholar]
  17. Marsden H. S., Crombie I. K., Subak-Sharpe J. H. 1976; Control of protein synthesis in herpesvirus-infected cells : analysis of the polypeptides induced by wild-type and sixteen temperature-sensitive mutants of HSV strain 17. Journal of General Virology 31:347–373
    [Google Scholar]
  18. Marsden H. S., Stow N. D., Preston V. G., Timbury M. C., Wilkie N. M. 1978; Physical mapping of herpes simplex virus-induced polypeptides. Journal of Virology 28:628–642
    [Google Scholar]
  19. Oostra B. A., Harvey R., Ely B. K., Markham A. F. 1983; Transforming activity of polyoma virus middle-T antigen probed by site-directed mutagenesis. Nature; London: 304:456–459
    [Google Scholar]
  20. Ritchie D. A., Brown S. M., Subak-Sharpe J. H., Jamieson A. T. 1977; Heterozygosis and genetic recombination in herpes simplex virus type 1. Virology 82:323–333
    [Google Scholar]
  21. Roizman B. 1979; The structure and isomerization of herpes simplex virus genomes. Cell 16:481–494
    [Google Scholar]
  22. Schaffer P. A., Tevethia M. J. 1974; Recombination between temperature-sensitive mutants of herpes simplex virus type 1. Virology 58:219–228
    [Google Scholar]
  23. Sharp J. A., Wagner M. J., Summers W. C. 1983; Transcription of herpes simplex virus genesin vivo: overlap of a late promoter with the 3ʹ end of the early thymidine kinase gene. Journal of Virology 45:10–17
    [Google Scholar]
  24. Stow N. D. 1981; Cloning of a DNA fragment from the left-hand terminus of the adenovirus type 5 genome and its use in site directed mutagenesis. Journal of Virology 37:171–180
    [Google Scholar]
  25. Stow N. D., Wilkie N. M. 1976; An improved technique for obtaining enhanced infectivity with herpes simplex virus type 1 DNA. Journal of General Virology 33:447–458
    [Google Scholar]
  26. Stow N. D., Subak-Sharpe I. H., Wilkie N. M. 1978; Physical mapping of herpes simplex virus type 1 mutations by marker rescue. Journal of Virology 28:182–192
    [Google Scholar]
  27. Szostak J. W., Orr-Weaver T. L., Rothstein R. J., Stahl F. W. 1983; The double-strand-break repair model for recombination. Cell 33:25–35
    [Google Scholar]
  28. Umene K. 1985; Intermolecular recombination of the herpes simplex type 1 genome analysed using two strains differing in restriction enzyme cleavage sites. Journal of General Virology 66:2659–2670
    [Google Scholar]
  29. Wagner M. J., Sharp J. A., Summers W. C. 1981; Nucleotide sequence of the thymidine kinase gene of herpes simplex virus type I. Proceedings of the National Academy of Sciences U.S.A: 781441–1445
    [Google Scholar]
  30. Weller S. K., Aschman D. P., Sacks W. R., Coen D. M., Schaffer P. A. 1983; Genetic analysis of temperaturesensitive mutants of HSV-1: the combined use of complementation and physical mapping for cistron assignment. Virology 130:290–305
    [Google Scholar]
  31. Wilkie N. M. 1976; Physical maps of herpes simplex type 1 DNA for restriction endonucleases 7/mdIII,Hpal and Xbal . Journal of Virology 20:222–223
    [Google Scholar]
  32. Young C. S. H., Silverstein S. J. 1980; The kinetics of adenovirus recombination in homotypic and heterotypic genetic crosses. Virology 101:503–515
    [Google Scholar]
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