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Aberrant tissue specific expression of the transgene in transgenic mice that carry the hepatitis B virus genome defective in the X gene

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Summary

The control mechanisms for the transgene expression in mice that carry the hepatitis B virus genome defective in the polymerase and X genes were analyzed. Ten lines of transgenic mouse were established, and in seven lines the surface and e antigens were detected in the serum. In transgenic mice from five lines examined, the transgene was markedly expressed in a broad spectrum of tissues including the kidney, heart, brain, muscle and intestine, but only poorly in the liver. In the kidney and heart the 3.5 kb and 2.1 kb mRNAs were expressed, whereas only the 0.8 kb and 4.0 kb mRNAs were detected in the testis and brain, respectively, suggesting that each of the mRNAs was transcribed through a different control mechanism. The surface, e and core antigens accumulated in the kidney and heart. DNA was hypomethylated at a region closely downstream of the enhancer in the liver, kidney and heart, and a DNase I hypersensitive site was detected upstream of the enhancer in these tissues. In the testis, however, the whole transgene was hypomethylated and the DNase I hypersensitive site was closer to the enhancer. These differences may be relevant to the preferential expression of the 0.8 kb mRNA in the testis, but cannot explain the inefficiency of transgene expression in the liver. Our observations suggest that the X protein is required for efficient expression of the viral gene in the liver but not in other tissues.

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References

  1. Akmal M, El-Ghor A, Burk RD (1989) DNase I hypersensitive site maps to the HBV enhancer. Virology 172: 478–488

    Google Scholar 

  2. Araki K, Miyazaki J, Hino O, Tomita N, Chisaka O, Matsubara K, Yamamura K (1989) Expression and replication of hepatitis B virus genome in transgenic mice. Proc Natl Acad Sci USA 86: 207–211

    Google Scholar 

  3. Araki K, Miyazaki J, Tsurimoto T, Inomoto T, Iwanaga T, Matsubara K, Yamamura K (1989) Demethylation by 5-azacytidine results in the expression of hepatitis B virus surface antigen in transgenic mice. Jpn J Cancer Res 80: 295–298

    Google Scholar 

  4. Babinet C, Farza H, Morello D, Hadchouel M, Pourcel C (1985) Specific expression of hepatitis B surface antigen (HBsAg) in transgenic mice. Science 230: 1160–1163

    Google Scholar 

  5. Becker P, Renkawitz R, Schutz G (1984) Tissue specific DNase I hypersensitive sites in the 5′-flanking sequences of the tryptophan oxygenase and the tyrosine aminotransferase genes. EMBO J 3: 2015–2020

    Google Scholar 

  6. Blum HE, Gerok W, Vyas GN (1989) The molecular biology of hepatitis B virus. Trends Genet 5: 154–158

    Google Scholar 

  7. Blum HE, Stowring L, Figus A, Montgomery CK, Haase AT, Vyas GN (1983) Detection of hepatitis B virus DNA in hepatocytes, bile duct epithelium, and vascular elements by in situ hybridization. Proc Natl Acad Sci USA 80: 6685–6688

    Google Scholar 

  8. Burk RD, Deloia JA, Elawady MK, Gearhart JD (1988) Tissue preferential expression of the hepatitis B virus (HBV) surface antigen gene in two lines of HBV transgenic mice. J Virol 62: 649–654

    Google Scholar 

  9. Cedar H (1988) DNA methylation and gene activity. Cell 53: 3–4

    Google Scholar 

  10. Chirgwin JM, Przybyla AE, MacDonald RJ, Rutter WJ (1979) Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry 18: 5294–5299

    Google Scholar 

  11. Chisari FV, Pinkert CA, Milich DR, Fillipi P, McLachlan A, Palmiter RD, Brinster RL (1985) A transgenic mouse model of the chronic hepatitis B surface antigen carrier state. Science 230: 1157–1160

    Google Scholar 

  12. Choo K-B, Liew L-N, Chong KY, Lu R, Cheng WTK (1991) Transgenome transcription and replication in the liver and extrahepatic tissues of a human hepatitis B virus transgenic mouse. Virology 182: 785–792

    Google Scholar 

  13. Dejean A, Lugassy C, Zafrani S, Tiollais P, Brechot C (1984) Detection of hepatitis B virus DNA in pancreas, kidney and skin of two human carriers of the virus. J Gen Virol 65: 651–655

    Google Scholar 

  14. Elgin SCR (1988) The formation and function of DNase I hypersensitive sites in the process of gene activation. J Biol Chem 263: 19259–19262

    Google Scholar 

  15. Faktor O, Shaul Y (1990) The identification of hepatitis B virus X gene responsive elements reveals functional similarity of X and HTLV-I tax. Oncogene 5: 867–872

    Google Scholar 

  16. Farza H, Hadechouel M, Scotto J, Tiollais P, Babinet C, Pourcel C (1988) Replication and gene expression of hepatitis B virus in a transgenic mouse that contains the complete viral genome. J Virol 62: 4144–4152

    Google Scholar 

  17. Fritton HP, Sippel AE, Igo-Kemenes T (1983) Nuclear-hypersensitive sites in the chromatin domain of the chicken lysozyme gene. Nucleic Acids Res 11: 3467–3485

    Google Scholar 

  18. Gocke DJ (1975) Extrahepatic manifestations of viral hepatitis. Am J Med Sci 270: 49–52

    Google Scholar 

  19. Guo W, Wang J, Tam G, Yen TSB, Ou J (1991) Leaky tanscription termination produces larger and smaller than genome size hepatitis B virus X gene transcripts. Virology 181: 630–636

    Google Scholar 

  20. Hadchouel M, Farza H, Simon D, Tiollais P, Pourcel C (1987) Maternal inhibition of hepatitis B surface antigen gene expression in transgenic mice correlates with de novo methylation. Nature 329: 454–456

    Google Scholar 

  21. Höhne M, Schaefer S, Seifer M, Feitelson MA, Paul D, Gerlich WH (1990) Malignant transformation of immortalized transgenic hepatocytes after transfection with hepatitis B virus DNA. EMBO J 9: 1137–1145

    Google Scholar 

  22. Hu K-Q, Siddiqui A (1991) Regulation of the hepatitis B virus gene expression by the enhancer element I. Virology 181: 721–726

    Google Scholar 

  23. Iwakura Y, Asano M, Nishimune Y, Kawada Y (1988) Male sterility of transgenic mice carrying exogenous mouse interferon-β gene under the control of the metallothionein enhancer-promoter. EMBO J 7: 3757–3762

    Google Scholar 

  24. Kim C-M, Koike K, Saito I, Miyamura T, Jay G (1991) HBx gene of hepatitis B virus induces liver cancer in transgenic mice. Nature 351: 317–320

    Google Scholar 

  25. Koike K, Shirakata Y, Yaginuma K, Arii M, Takada S, Nakamura I, Hayashi Y, Kawada M, Kobayashi M (1989) Oncogenic potential of hepatitis B virus. Mol Biol Med 6: 151–160

    Google Scholar 

  26. Lai KN, Lai FM-M, Lo S, Leung A (1987) Is there a pathogenetic role of hepatitis B in lupus nephritis? Arch Pathol Lab Med 111: 185–188

    Google Scholar 

  27. Landschulz WH, Johnson PF, Adashi EY, Graves BJ, McKnight SL (1988) Isolation of a recombinant copy of the gene encoding C/EBP. Genes Dev 2: 786–800

    Google Scholar 

  28. Laure F, Zagury D, Saimot AG, Gallo RC, Hahn BH, Brechot C (1985) Hepatitis B virus DNA sequences in lymphoid cells from patients with AIDS and AIDS-related complex. Science 229: 561–563

    Google Scholar 

  29. Melton DA, Krieg PA, Rebagliati MR, Maniatis T, Zinn K, Green MR (1984) Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP 6 promoter. Nucleic Acids Res 12: 7035–7056

    Google Scholar 

  30. Miller RH, Robinson W (1983) Integrated hepatitis B virus DNA sequences specifying the major viral core polypeptide are methylated in PLC/PRF/5 cells. Proc Natl Acad Sci USA 80: 2534–2538

    Google Scholar 

  31. Okamoto H, Imai M, Shimozaki M, Hoshi Y, Iizaka H, Gotanda T, Tsuda F, Miyakawa Y, Mayumi M (1986) Nucleotide sequence of a cloned hepatitis B virus genome, subtype ayr: comparison with genomes of the other three subtypes. J Gen Virol 67: 2305–2314

    Google Scholar 

  32. Poli V, Mancini FP, Cortese R (1990) IL-6 DBP, a nuclear protein involved in interleukin-6 signal transduction, defines a new family of leucine zipper proteins related to C/EBP. Cell 63: 643–653

    Google Scholar 

  33. Pontisso P, Locasciulli A, Schiavon E, Cattoretti G, Schiro R, Stenico D, Alberti A (1987) Detection of hepatitis B virus DNA sequences in bone marrow of children with leukemia. Cancer 59: 292–296

    Google Scholar 

  34. Pourcel C, Tiollais P, Farza H (1990) Transcription of the S gene in transgenic mice is associated with hypomethylation at specific sites and with DNase I sensitivity. J Virol 64: 931–935

    Google Scholar 

  35. Roman C, Platero JS, Shuman J, Calame K (1990) Ig/EBP-1: a ubiquitously expressed immunoglobulin enhancer binding protein that is similar to C/EBP and heterodimerizes with C/EBP. Genes Dev 4: 1404–1415

    Google Scholar 

  36. Schumacher HR, Gall EP (1974) Arthritis in acute hepatitis and chronic active hepatitis. Pathology of the synovial membrane with evidence for the presence of Australia antigen in synovial membranes. Am J Med 57: 655–664

    Google Scholar 

  37. Seto E, Yen TSB, Peterlin BM, Ou JH (1988) Transactivation of the human immunodeficiency virus long terminal repeat by the hepatitis B virus X protein. Proc Natl Acad Sci USA 85: 8286–8290

    Google Scholar 

  38. Siddqui A (1983) Hepatitis B virus DNA in Kaposi sarcoma. Proc Natl Acad Sci USA 80: 4861–4864

    Google Scholar 

  39. Somlo F (1989) Localization of hepatitis B virus in a primary testicular cancer. Arch Pathol Lab Med 113: 1184–1186

    Google Scholar 

  40. Spandau DF, Lee CH (1988) Trans-activation of viral enhancers by the hepatitis B virus X protein. J Virol 62: 427–434

    Google Scholar 

  41. Takada S, Koike K (1990) Trans-activation function of a 3′ truncated X gene-cell fusion product from integrated hepatitis B virus DNA in chronic hepatitis tissues. Proc Natl Acad Sci USA 87: 5628–5632

    Google Scholar 

  42. Thomas PS (1980) Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc Natl Acad Sci USA 77: 5201–5205

    Google Scholar 

  43. Tiollais P, Pourcel C, Dejean A (1985) The hepatitis B virus. Nature 317: 489–495

    Google Scholar 

  44. Twu JS, Schloemer RH (1987) Transcriptionaltrans-activating function of hepatitis B virus. J Virol 61: 3448–3453

    Google Scholar 

  45. Vannice JL, Levinson AD (1988) Properties of the human hepatitis B virus enhancer: position effects and cell-type nonspecificity. J Virol 62: 1305–1313

    Google Scholar 

  46. Weiss TD, Tsai CC, Baldassare AR, Zuckner J (1978) Skin lesions in viral hepatitis. Am J Med 64: 269–273

    Google Scholar 

  47. Wollershein M, Debelka U, Hofschneider PH (1988) A transactivating function encoded in the hepatitis B virus X gene is conserved in the integrated state. Oncogene 3: 545–552

    Google Scholar 

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Nagashima, H., Imai, M. & Iwakura, Y. Aberrant tissue specific expression of the transgene in transgenic mice that carry the hepatitis B virus genome defective in the X gene. Archives of Virology 132, 381–397 (1993). https://doi.org/10.1007/BF01309547

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