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Effect of herpes simplex virus type-1 UL41 gene on the stability of mRNA from the cellular genes: β-actin, fibronectin, glucose transporter-1, and docking protein, and on virus intraperitoneal pathogenicity to newborn mice

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Abstract

Infection with HSV-1 is accompanied by the shut-off of cellular gene expression. The virion-associated function is encoded by the viral gene UL41. An HSV-1 mutant, vhs-1, which has a genomic deletion in the UL41 gene, is incapable of inducing the shut-off of cellular gene expression. The effect of HSV-1 infection on the shut-off of the cellular genes (or mRNA degradation) was studied specifically with the cellular genes for β-actin, fibronectin, glucose transporter-1, and the docking protein. The level of these specific mRNAs was measured in cells infected with several HSV-1 strains and was compared to that of vhs-1- and mock-infected cells. It was possible to demonstrate a marked reduction in the level of the specific mRNA from these cellular genes in cells infected with several HSV-1 strains but not with the vhs-1 mutant. The pathogenicity of the HSV-1 vhs-1 mutant to newborn mice was studied. It was found that the mutant is less pathogenic to newborn mice than its parental strain HSV-1 KOS.

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References

  1. Fenwick M.L. and Walker M.J., J Gen Virol41 37–51, 1978.

    Google Scholar 

  2. Sidiskis R.J. and Roizman B., Science153 76–78, 1966.

    Google Scholar 

  3. Nishioka Y. and Silverstern S., J Gen Virol27 619–627, 1978.

    Google Scholar 

  4. Fenwick M.L. and Everett R.D., J Gen Virol71 2961–2967, 1990.

    Google Scholar 

  5. Fenwick M.L. and McMenamin M.M., J Gen Virol65 1225–1228, 1984.

    Google Scholar 

  6. Mayman B.A. and Nishioka Y., J Virol53 1–6, 1985.

    Google Scholar 

  7. Scheck N. and Bachenheimer S.L., J Virol55 601–610, 1985.

    Google Scholar 

  8. Kwong A.D., Kruger J.A., and Frenkel N., J Virol62 912–921, 1988.

    Google Scholar 

  9. Strom T. and Frenkel N., J Virol6 2198–2207, 1978.

    Google Scholar 

  10. Everett R.D. and Fenwick M.L., J Gen Virol71 1387–1390, 1990.

    Google Scholar 

  11. Bastow K.F., Zhou B.S., and Chang Y.C., Virus Genes2 357–365, 1989.

    Google Scholar 

  12. Daksis J.I. and Chan V.L., J Virol61 143–150, 1987.

    Google Scholar 

  13. Enk C., Sprecher E., and Becker Y., Arch Virol121 141–151, 1991.

    Google Scholar 

  14. Dienes H.P., Knoblich A., and Falke D., Arch Virol86 223–237, 1975.

    Google Scholar 

  15. Ruoslathi E., Ann Rev Biochem57 375–413, 1988.

    Google Scholar 

  16. Filer J.S., Muckler M., McCall A.L., and Lodish H.F., J Clin Invest79 657–661, 1987.

    Google Scholar 

  17. Wickner W.T. and Lodish H.F., Science230 400–407, 1985.

    Google Scholar 

  18. Wessels H.P. and Spiess M., Cell55 61–70, 1988.

    Google Scholar 

  19. Von Heijne G., EMBO J.5 3021–3027, 1986.

    Google Scholar 

  20. Saier M.H., Werner P.K., and Müller M., Microbiol Rev53 333–366, 1989.

    Google Scholar 

  21. Rösen A., Ernst E., Koch H.G., Gelderblom H., Darai G., Hadar J., Tabor E., Ben Hur T., and Becker Y., Virus Res5 157–175, 1986.

    Google Scholar 

  22. Becker Y., Hadar J., Tabor E., Ben Hurt T., Raibstein I., Rösen A., and Dari G., Virology149 255–259, 1986.

    Google Scholar 

  23. Rösen A., Gelderblom H., and Darai G., Med Microbiol Immunol173 257–278, 1985.

    Google Scholar 

  24. Aldberg A., Linney E., and Ruoslahti E., J Biol Chem258 10193–10196, 1988.

    Google Scholar 

  25. Flier J.S., Mueckler M., McCall A.L., and Lodish H.F.J., Clin Invest79 657–661, 1987.

    Google Scholar 

  26. Muckler M., Carnso C., Baldwin S.A., Pancio M., Blench I., and Moris H.R., Science229 941, 1985.

    Google Scholar 

  27. Chirgwin J.M., Przybyla A.E., MacDonald R.S., and Rutter W.S., Biochemistry18 5294–5299, 1979.

    Google Scholar 

  28. Thomas P.S., Proc Natl Acad Sci USA71 5201–5205, 1980.

    Google Scholar 

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Becker, Y., Tavor, E., Asher, Y. et al. Effect of herpes simplex virus type-1 UL41 gene on the stability of mRNA from the cellular genes: β-actin, fibronectin, glucose transporter-1, and docking protein, and on virus intraperitoneal pathogenicity to newborn mice. Virus Genes 7, 133–143 (1993). https://doi.org/10.1007/BF01702393

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  • DOI: https://doi.org/10.1007/BF01702393

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