This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Raney, A. K.
Right arrow Articles by McLachlan, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Raney, A. K.
Right arrow Articles by McLachlan, A.

 Previous Article  |  Next Article 

Journal of Virology, March 2001, p. 2900-2911, Vol. 75, No. 6
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.6.2900-2911.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Nuclear Covalently Closed Circular Viral Genomic DNA in the Liver of Hepatocyte Nuclear Factor 1alpha -Null Hepatitis B Virus Transgenic Mice†

Anneke K. Raney,1 Carrie M. Eggers,1 Eric F. Kline,1 Luca G. Guidotti,2 Marco Pontoglio,3 Moshe Yaniv,3 and Alan McLachlan1,*

Department of Cell Biology1 and Department of Molecular and Experimental Medicine,2 The Scripps Research Institute, La Jolla, California 92037, and Unité des Virus Oncogènes, UA1644 du CNRS, Départment des Biotechnologies, Institut Pasteur, Paris, France3

Received 29 August 2000/Accepted 11 December 2000

The role of hepatocyte nuclear factor 1alpha (HNF1alpha ) in the regulation of hepatitis B virus (HBV) transcription and replication in vivo was investigated using a HNF1alpha -null HBV transgenic mouse model. HBV transcription was not measurably affected by the absence of the HNF1alpha transcription factor. However, intracellular viral replication intermediates were increased two- to fourfold in mice lacking functional HNF1alpha protein. The increase in encapsidated cytoplasmic replication intermediates in HNF1alpha -null HBV transgenic mice was associated with the appearance of nonencapsidated nuclear covalently closed circular (CCC) viral genomic DNA. Viral CCC DNA was not readily detected in HNF1alpha -expressing HBV transgenic mice. This indicates the synthesis of nuclear HBV CCC DNA, the proposed viral transcriptional template found in natural infection, is regulated either by subtle alterations in the levels of viral transcripts or by changes in the physiological state of the hepatocyte in this in vivo model of HBV replication.


* Corresponding author. Mailing address: Department of Cell Biology, The Scripps Research Institute, 10550 N. Torrey Pines Rd., La Jolla, CA 92037. Phone: (858) 784-8097. Fax: (858) 784-2513. E-mail: mclach{at}scripps.edu.

dagger Publication no. 13419-CB from The Scripps Research Institute.


Journal of Virology, March 2001, p. 2900-2911, Vol. 75, No. 6
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.6.2900-2911.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Oropeza, C. E., Li, L., McLachlan, A. (2008). Differential Inhibition of Nuclear Hormone Receptor-Dependent Hepatitis B Virus Replication by the Small Heterodimer Partner. J. Virol. 82: 3814-3821 [Abstract] [Full Text]  
  • Guo, H., Jiang, D., Zhou, T., Cuconati, A., Block, T. M., Guo, J.-T. (2007). Characterization of the Intracellular Deproteinized Relaxed Circular DNA of Hepatitis B Virus: an Intermediate of Covalently Closed Circular DNA Formation. J. Virol. 81: 12472-12484 [Abstract] [Full Text]  
  • Gao, W., Hu, J. (2007). Formation of Hepatitis B Virus Covalently Closed Circular DNA: Removal of Genome-Linked Protein. J. Virol. 81: 6164-6174 [Abstract] [Full Text]  
  • Anderson, A. L., Banks, K. E., Pontoglio, M., Yaniv, M., McLachlan, A. (2005). Alpha/Beta Interferon Differentially Modulates the Clearance of Cytoplasmic Encapsidated Replication Intermediates and Nuclear Covalently Closed Circular Hepatitis B Virus (HBV) DNA from the Livers of Hepatocyte Nuclear Factor 1{alpha}-Null HBV Transgenic Mice. J. Virol. 79: 11045-11052 [Abstract] [Full Text]  
  • Wieland, S. F., Spangenberg, H. C., Thimme, R., Purcell, R. H., Chisari, F. V. (2004). Expansion and contraction of the hepatitis B virus transcriptional template in infected chimpanzees. Proc. Natl. Acad. Sci. USA 101: 2129-2134 [Abstract] [Full Text]  
  • Doitsh, G., Shaul, Y. (2004). Enhancer I Predominance in Hepatitis B Virus Gene Expression. Mol. Cell. Biol. 24: 1799-1808 [Abstract] [Full Text]  
  • Uprichard, S. L., Wieland, S. F., Althage, A., Chisari, F. V. (2003). Transcriptional and posttranscriptional control of hepatitis B virus gene expression. Proc. Natl. Acad. Sci. USA 100: 1310-1315 [Abstract] [Full Text]  
  • Abdelhamed, A. M., Kelley, C. M., Miller, T. G., Furman, P. A., Cable, E. E., Isom, H. C. (2003). Comparison of Anti-Hepatitis B Virus Activities of Lamivudine and Clevudine by a Quantitative Assay. Antimicrob. Agents Chemother. 47: 324-336 [Abstract] [Full Text]  
  • Yang, P. L., Althage, A., Chung, J., Chisari, F. V. (2002). Hydrodynamic injection of viral DNA: A mouse model of acute hepatitis B virus infection. Proc. Natl. Acad. Sci. USA 99: 13825-13830 [Abstract] [Full Text]  
  • Rang, A., Bruns, M., Heise, T., Will, H. (2002). Antiviral Activity of Interferon-alpha against Hepatitis B Virus Can Be Studied in Non-hepatic Cells and Is Independent of MxA. J. Biol. Chem. 277: 7645-7647 [Abstract] [Full Text]