Summary
It has previously been shown that the hepatitis B virus (HBV) X gene product, HBx, transactivates homologous and heterologous transcriptional regulatory sequences of viruses, including the human immunodeficiency virus type 1 (HIV1) long terminal repeat (LTR), and various cellular genes in vitro. To evaluate the transactivating function of HBx in vivo, we generated transgenic mice carrying the X open reading frame under the control of the human antithrombin III (ATIII) gene regulatory sequences. These mice express the 16 Kd HBx protein in the liver, as demostrated by immunoprecipitation studies. Crossbreeding of HBx mice with transgenics carrying either the chloramphenicol acetyl transferase (CAT) bacterial or the lacZ reporter gene driven by the HIV1-LTR allowed us to demostrate, for the first time, the in vivo transactivating function of HBx protein.
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© 1993 Springer-Verlag
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Balsano, C. et al. (1993). The hepatitis B virus X gene product transactivates the HIV-LTR in vivo. In: Gerlich, W.H. (eds) Research in Chronic Viral Hepatitis. Archives of Virology Supplementum, vol 8. Springer, Vienna. https://doi.org/10.1007/978-3-7091-9312-9_7
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DOI: https://doi.org/10.1007/978-3-7091-9312-9_7
Publisher Name: Springer, Vienna
Print ISBN: 978-3-211-82497-9
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