1887

Abstract

Human cytomegalovirus (HCMV) open reading frame UL32 codes for the basic phosphoprotein pp150 (ppUL32), an abundant constituent of the virion tegument. In order to study its potential role in the assembly and/or transport of progeny particles, astrocytoma cell lines (U373MG) were generated, stably expressing a 2·1 kb 5′ fragment of UL32 in antisense orientation under the control of the HCMV major immediate early promoter. The steady-state level of the UL32 sense mRNA and pp150 synthesis were strongly reduced in infected antisense cell lines. Neither immediate early and early gene expression, nor viral DNA replication, was inhibited; the expression of the late gene product gB (gpUL55) was also reduced, but mainly at the level of translation. Control experiments indicated that this differential effect of UL32 antisense expression on the synthesis of viral products was specific. As a consequence of the inhibitory effect, virus yield was significantly reduced in antisense mRNA cell lines. Ultrastructural comparison of control and antisense cells revealed no difference in nucleocapsid forms in the nucleus. However, in the cytoplasm of antisense cells, DNA-containing C capsids and virions were absent and abnormal forms of non-infectious enveloped particles were observed. The data suggest the involvement of pp150 either in the transport of DNA-containing particles through the nuclear envelope or in the stabilization of capsids in the cytoplasm. Thus, UL32 antisense mRNA appears to interfere strongly with virus maturation during the late phase of the infectious cycle.

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1997-10-01
2024-04-20
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References

  1. Alford C. A., Britt W. J. 1993; Cytomegalovirus. In The Herpesviruses pp 227–255 Roizman B., Whitley R. J., Lopez C. Edited by New York: Raven Press;
    [Google Scholar]
  2. Baldick C. J., Shenk T. 1996; Proteins associated with purified human cytomegalovirus particles. Journal of Virology 70:6097–6105
    [Google Scholar]
  3. Bankier A. T., Beck S., Bohni R., Brown C. M., Cerny R., Chee M. S., Hutchinson C. A., Kouzarides T., Martignetti J. A., Preddie E., Satchwell S. C., Tomlinson P., Weston K. M., Barrell B. G. 1991; The DNA sequence of the human cytomegalovirus genome. DNA Sequences 2:1–12
    [Google Scholar]
  4. Benko D., Gibson W. 1989; A major tegument phosphoprotein of human cytomegalovirus contains O-linked GlcNAc. In Cell Biology of Virus Entry, Replication, and Pathogenesis pp 57–66 Compans R. W., Helenius A., Oldstone M. B. A. Edited by New York: A. R. Liss;
    [Google Scholar]
  5. Bryant L. A., Sinclair J. H. 1993; Inhibition of human cytomegalovirus major immediate early gene expression by antisense RNA expression vectors. Journal of General Virology 74:1965–1967
    [Google Scholar]
  6. Dal Monte P., Bessia C., Ripalti A., Landini M. P., Topilko A., Plachter B., Virelizier J. L., Michelson S. 1996; Stably expressed antisense RNA to cytomegalovirus UL83 inhibits viral replication. Journal of Virology 70:2086–2094
    [Google Scholar]
  7. Fleckenstein B., Müller I., Collins J. 1982; Cloning of the complete human cytomegalovirus genome in cosmids. Gene 18:39–46
    [Google Scholar]
  8. Gibson W. 1983; Protein counterparts of human and simian cytomegaloviruses. Virology 128:391–406
    [Google Scholar]
  9. Greis K. D., Gibson W., Hart G. W. 1994; Site-specific glycosylation of the human cytomegalovirus tegument basic phosphoprotein (UL32) at serine 921 and serine 952. Journal of Virology 68:8339–8349
    [Google Scholar]
  10. Griffith G., Rottier P. 1992; Cell biology of viruses that assemble along the biosynthetic pathway. Seminars in Cell Biology 3:367–381
    [Google Scholar]
  11. Hensel G., Meyer H. H., Gärtner S., Brand G., Kern H. F. 1995; Nuclear localization of the human cytomegalovirus tegument protein pp150 (ppUL32). Journal of General Virology 76:1591–1601
    [Google Scholar]
  12. Hensel G., Meyer H. H., Buchmann I., Schmolke S., Plachter B., Radsak K., Kern H. F. 1996; Intracellular localization and expression of the human cytomegalovirus matrix phosphoprotein pp71 (ppUL82): evidence for its translocation into the nucleus. Journal of General Virology 77:3087–3097
    [Google Scholar]
  13. Irmiere A., Gibson W. 1983; Isolation and characterization of a noninfectious virion-like particle released from cells infected with human strains of cytomegalovirus. Virology 130:118–133
    [Google Scholar]
  14. Jahn G., Kouzarides T., Mach M., Scholl B. C., Plachter B., Traube B., Preddie E., Satchwell S. C., Fleckenstein B., Barrell B. G. 1987; Map position and nucleotide sequence of the gene for the large structural phosphoprotein of human cytomegalovirus. Journal of Virology 61:1358–1367
    [Google Scholar]
  15. Jones T. R., Muzithras V. P. 1992; A cluster of dispensable genes within the human cytomegalovirus genome short component: IRS1, US1 through US5, and the US6 family. Journal of Virology 66:2541–2546
    [Google Scholar]
  16. Kim S. K., Wold B. J. 1985; Stable reduction of thymidine kinase activity in cells expressing high levels of antisense RNA. Cell 42:129–138
    [Google Scholar]
  17. Liu B., Stinski M. F. 1992; Human cytomegalovirus contains a tegument protein that enhances transcription from promoter with upstream ATF and AP-1 cis-acting elements. Journal of Virology 66:4434–4444
    [Google Scholar]
  18. Lucin P., Jonjic S., Messerle M., Polic B., Hengel H., Koszinowski U. H. 1994; Late phase inhibition of murine cytomegalovirus replication by synergistic action of interferon-gamma and tumor necrosis factor. Journal of General Virology 75:101–110
    [Google Scholar]
  19. Mocarski E. S. 1996; Cytomegaloviruses and their replication. In Fields Virology, 3rd edn. pp 2447–2492 Fields B. N., Knipe D. M., Howley P. M. Edited by Philadelphia: Lippincott-Raven;
    [Google Scholar]
  20. Neipel F., Ellinger K., Fleckenstein B. 1992; Gene for the major antigenic protein (p100) of human herpesvirus 6. Journal of Virology 66:3918–3924
    [Google Scholar]
  21. Nellen W., Lichtenstein C. 1993; What makes an mRNA anti-sense- itive?. Trends in Biochemical Science 18:419–423
    [Google Scholar]
  22. Peeples M. E. 1991; Paramyxovirus M proteins: pulling it all together and taking it on the road. In The Paramyxoviruses pp 427–456 Kingsbury D. W. Edited by New York & London: Plenum Press;
    [Google Scholar]
  23. Plachter B., Nordin M., Zweygberg Wirgart B., Mach M., Stein H., Grillner L., Jahn G. 1992; The DNA-binding protein p52 of human cytomegalovirus reacts with monoclonal antibody CCH2 and associates with the nuclear membrane at late times after infection. Virus Research 24:265–276
    [Google Scholar]
  24. Radsak K., Brücher H., Britt W., Shiou H., Schneider D., Kollert A. 1990; Nuclear compartmentation of glycoprotein B of human cytomegalovirus. Virology 177:515–522
    [Google Scholar]
  25. Radsak K., Bröcher K. H., Georgatos S. D. 1991; Focal nuclear envelope lesions and specific nuclear lamin A/C dephosphorylation during infection with human cytomegalovirus. European Journal of Cell Biology 54:299–304
    [Google Scholar]
  26. Ripalti A., Boccuni M. C., Campanini F., Landini M. P. 1995; Cytomegalovirus-mediated induction of antisense mRNA expression to UL44 inhibits viral replication in an astrocytoma cell line : identification of an essential gene. Journal of Virology 69:2047–2057
    [Google Scholar]
  27. Rixon F. J. 1993; Structure and assembly of herpes viruses. Seminars in Virology 4:135–144
    [Google Scholar]
  28. Roizman B., Sears A. E. 1996; Herpes simplex viruses and their replication. In Fields Virology, 3rd edn. pp 2231–2295 Fields B. N., Knipe D. M., Howley P. M. Edited by Philadelphia: Lippincott-Raven;
    [Google Scholar]
  29. Sambrook J., Fritsch E. F., Maniatis T. 1989 Molecular Cloning: A Laboratory Manual, 2nd edn.. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory;
    [Google Scholar]
  30. Schmolke S., Drescher P., Jahn G., Plachter B. 1995a; Nuclear targeting of the tegument protein pp65 (UL83) of human cyto-megalovirus : an unusual bipartite nuclear localization signal functions with other portions of the protein to mediate its efficient nuclear transport. Journal of Virology 69:1071–1078
    [Google Scholar]
  31. Schmolke S., Kern H. F., Drescher P., Jahn G., Plachter B. 1995b; The dominant phosphoprotein pp65 (UL83) of human cytomegalovirus is dispensable for growth in cell culture. Journal of Virology 65:5959–5968
    [Google Scholar]
  32. Scholl B. C., Von Hintenstern J., Borisch B., Traupe B., Bröker M., Jahn G. 1988; Prokaryotic expression of immunogenic polypeptides of the large phosphoprotein (pp150) of human cytomegalovirus. Journal of General Virology 69:1195–1204
    [Google Scholar]
  33. Severi B., Landini M. P., Govoni E. 1988; Human cytomegalovirus morphogenesis : an ultrastructural study of the late cytoplasmic phases. Archives of Virology 98:51–64
    [Google Scholar]
  34. Severi B., Landini M. P., Cenacchi G., Zini N., Maraldi N. M. 1992; Human cytomegalovirus nuclear and cytoplasmic dense bodies. Archives of Virology 123:193–207
    [Google Scholar]
  35. Somogyi B., Michelson S., Masse M. J. O. 1990; Genomic localization of a human cytomegalovirus protein with protein kinase activity (PK68). Virology 174:276–285
    [Google Scholar]
  36. Spaete R., Thayer R., Probert W., Maiarz F., Chamberlain S., Rasmussen L., Merigan T., Pachl C. 1988; Human cytomegalovirus strain Towne glycoprotein B is processed by proteolytic cleavage. Virology 174:276–285
    [Google Scholar]
  37. Spaete R., Gehrz R. C., Landini M. P. 1994; Human cyto-megalovirus structural proteins. Journal of General Virology 75:3287–3308
    [Google Scholar]
  38. Tooze J., Hollinshead M., Reis B., Radsak K., Kern H. F. 1992; Progeny vaccinia and human cytomegalovirus particles utilize early endosomal cisternae for their envelopes. European Journal of Cell Biology 60:163–178
    [Google Scholar]
  39. Weiner D., Gibson W. 1983; Phosphorylation, maturational processing and relatedness of strain Colburn matrix proteins. Virology 129:155–169
    [Google Scholar]
  40. Wills J. W., Crawen R. C. 1991; Form, function, and use of retroviral gag proteins. AIDS 5:639–652
    [Google Scholar]
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