Expression of Human Cytomegalovirus Immediate Early US3 Gene in Human Fibroblast Cells

  • Lee, Gyu-Cheol (Department of Microbiology, Chungbuk National University) ;
  • Lee, Chong-Kyo (Korea Research Institute of Chemical Technology) ;
  • Ahn, Jin-Hyun (Department of Pharmacology and Molecular Sciences, Johns Hopkins University Medical School) ;
  • Lee, Chan-Hee (Research Institute for Genetic Engineering, Chungbuk National University)
  • Published : 2000.03.01

Abstract

US3 gene is a member of the human cytomegalovirus (HCMV) immediate early gene. Although the precise functions of the US3 gene in HCMV replication and pathogenesis are not known, it has been reported to play a role in inhibiting major histocompatibility class I antigen presentation. For further knowledge of US3 gene expression, rabbit polyclonal antiserum of the US3 gene product was used for indirect immunofluorescence assay. In permissive human foreskin fibroblast (HFF) cells, US3 gene expression was detectable as crescent or half-moon shape in the perinuclear region at immediate early times after virus infection. HFF cells infected with mutant HCMV lacking US3 open reading frames were negative for US3 immunofluorescence assay. Double immunofluorescence assay using monoclonal antibody to gamma adaptin (specific for the Golgi complex) and rabbit anti-US3 antiserum revealed that US3 gene product could be localized to the Golgi complex. At later time after HCMV infection, US3 gene products were detected as globular aggregates in the cytosol. These aggregates were positive for gamma adaptin and stained with preimmune serum, suggesting a nonspecific reaction to the Golgi complex. Northern blot analysis revealed that transcription of US3 was observed only during immediate early times after virus infection (until 6 h postinfection). Therefore US3 gene expression appears to be confined to immediate early time and its gene products are localized to the Golgi complex as crescent shaped forms in the perinuclear cytoplasm.

Keywords

References

  1. Proc. Natl. Acad. Sci. USA 93 Human cytomegalovirus inhibits antigen presentation by a sequential multistep process Ahn, K.S.;A. Angulo;P. Ghazal;P.A. Perterson;Y. Yang;K. Fruh
  2. Immunity 6 The ER-lumimal domainof the HCMV glycoprotein US6 inhibits peptide translocation by TAP Ahn, K.S.;A. Gruhler;B. Galocha;T.R. Jones;E.J. H.J. Wiertz;H.L. Pioegh;P.A. Peterson;Y. Yang;K. Fruh
  3. J. Virol. v.68 The herpes simplex virus UL20 protein compensates for the differential disruption of exocytosis of virons and viral membrane glycoproteins associated with fragmentation of the Golgi apparatus Avitable, E.;P.L. Ward;C.D. Lazzaro;M.R. Torrisi;B. Roizman;G. Campadelli-Fiume
  4. J. Virol. v.69 Redistribution of microtubules and Golgi apparatus in herpes simplex virus-infected cells and their role in viral exocytosis Avitabile, E.;S.D. Gaeta;M.R. Torrisi;P.L. Ward;B. Roizman;G. Campadelli-Fiume
  5. Semin. Cell. Dev. Biol. v.7 Disassembly and reassembly of the Golgi apparatus Barr, F.A.;G. Warren
  6. J. Virol. v.69 IE2 protein is insufficient for transcriptional repression of the human cytomegalovirus US3 promoter Biegalke, B.J.
  7. J. Virol. v.71 IE2 protein is insufficient for transcriptional repression of the human cytomegalovirus US3 promoter Biegalke, B.J.
  8. J. Virol. v.72 Characterization of the transcriptional repressive element of the human cytomegalovirus immediate-early US3 gene Biegalke, B.J.
  9. J. Virol. v.70 Two distinct upstream regulatory domains containing multicopy cellular transcription factor binding sites provide basal repression and inducible enhancer characteristics to the immediate-early IES(US3) promoter from human cytomegalovirus Chan, Y.J.;W.P. Tseng;G.S. Hayward
  10. Curr. Top. Microbiol. Immunol. v.154 Anlaysis of the protein-coding content of the sequence of human cytomegalovirus strain AD169 Chee, M.S.;A.T. Bankier;S. Beck;R. Bohni;C.M. Brown;R. Cerny;T. Horsnell;C.A. Hutchison;T. Kouzarides;J.A. Martignetti;E. Preddie;S.C. Satchwell;P. Tomlinson;K.M. Weston;B.G. Barrell
  11. J. Virol. v.66 Human cytomegalovirus US3 and UL36-38 immediate-early proteins regulate gene expression Colberg-Poley, A.M.;L.D. Santomenna;P.P. Harlow;P.A. Benfield;D.J. Tenney
  12. J. Virol. v.35 Patterns of transcription of human cytomegalovirus in permissively infected cells DeMarchi, J.M.;C.A. Schmidit;A.S. Kaplan
  13. J. Gen. Virol. v.77 Human cytomegalovirus inhibits peptide translocation into the endoplasmic reticulum for MHCⅠ assembly Hengel, H.;Flohr, T.;Hammerling, G.J.;Kosznowski, U.H.;Mombery, F.
  14. J. Virol. v.61 Identification and characterization of the human cytomegalovirus immediate-early region 2 gene that stimulated gene expression from an inducible promoter Hermiston, T.W.;C.L. Malone;P.R. Witte;M.F. Stinski
  15. J. Virol. v.66 A cluster of dispensable genes within the human cytomegalovirus genome short component: IRS1,US1 through US5,and the US6 family Jones, T.R.;V.P. Muzithras
  16. J. Virol. v.71 Human cytomegalovirus US2 destabilizes major histocompatibility complex class I heavy chains Jones, T.R.;L. Sun
  17. J. Virol. v.68 Coronavirus M proteins accumulate in the Golgi complex beyond the site of virion budding Klumperman, J.;J.K. Locker;A. Meijer;M.C. Horzinek;H.J. Geuze;P.J.M. Rottier
  18. J. Virol. v.65 A 15-kilo-base-pair region of the human cytomegalovirus genome which includes US1 through US13 is dispensable for growth in cell culture Kollert-Jones, A.;E. Bogner;K. Radsak
  19. J. Virol. v.72 A cis repression sequence adjacent to the transcription start site of human cytomegalovirus US3 gene is required to down regulate gene expression at early and late times after infection Lashmit, P.E.;M.F. Stinski;E.A. Murphy;G.C. Bullock
  20. J. Virol. v.125 Transcription in human fibroblasts permissively infected by human cytomegalovirus strain AD169 McDonough, S.M.;D.H. Spector
  21. J. Virol. v.68 Assembly of vaccinia virus: the second wrapping cisterna is derived from the trans Golgi network Schmelz, M.;B. Sodeik;M. Ericsson;E.J. Wolffe;H. Shida;G. Hiller;G. Grffiths
  22. Arch. Virol. v.98 Human cytomegalovirus morphogenesis: and ultrastructural study of the late cytoplasmic phases Severi, B.;M.P. Landini;E. Govoni
  23. Ann. Rev. Cell Dev. Biol. v.12 Signal-mediated sorting of membrane proteins between the endoplasmic reticulum and the Golgi apparatus Teasdale, R.D.;M.R. Jacson
  24. J. Virol. v.65 Human cytomegalovirus UL36-38 and US3 immediate-earl genes" temporolly regulated expression of nuclear, cytoplasmic, and polysome-associated transcripts during infection Tenney, D.J.;A.M. Colberg-poley
  25. J. Virol. v.70 Regualtion of a human cytomegalovirus immediate-early gene(US3) by a silencer-enhancer combiantion Thrower, A.R.;G.C. Bullock;J.E. Bissell;M. F. Stinski
  26. J. Virol. v.66 A cellular function is required for pseudorabies virus envelope glycoprotein processing and virus egress Whealy, M.E.;A.K. Robbins;F. Tufaro;L.W. Enguist
  27. The human cytomegalovirus US11 gene product dislocates MHC class I heavy chains from endoreticulum to the cytosol v.Cell 84 Wiertz, E.;Jones, T.R.;Sun, L.;Bogyo, M.;Geuze, H.J.;Ploegh, H.
  28. J. Virol. v.69 Envelopment of varicella-zoster virus: targeting of glycoproteins to the trans-Golgi network Zhu, Z.;M.D. Gershon;Y. Hao;R.T. Ambron;C.A. Gabel;A.A. Gershon