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 Walker, M. P.
Right arrow Articles by Lipkin, W. I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Walker, M. P.
Right arrow Articles by Lipkin, W. I.

 Previous Article  |  Next Article 

Journal of Virology, May 2000, p. 4425-4428, Vol. 74, No. 9
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Expression and Characterization of the Borna Disease Virus Polymerase

Michelle Portlance Walker, Ingo Jordan, Thomas Briese, Nicole Fischer, and W. Ian Lipkin*

Emerging Diseases Laboratory, Departments of Neurology, Anatomy and Neurobiology, and Microbiology and Molecular Genetics, University of California, Irvine, California 92697-4292

Received 11 October 1999/Accepted 29 January 2000

Borna disease virus is the prototype of a new family, Bornaviridae, within the order Mononegavirales, that is characterized by nuclear transcription, splicing, low level replication, and neurotropism. The products of five open reading frames predicted from the genomic sequence have been confirmed; however, expression of the sixth, corresponding to the putative viral polymerase (L), has not been demonstrated. Here, we describe expression and characterization of a 190-kDa protein proposed to represent L. Expression of this protein from the third transcription unit of the viral genome is dependent on a splicing event that fuses a small upstream open reading frame in frame with the larger downstream continuous open reading frame. The protein is detected by serum antibodies from infected rats and is present in the nucleus, where it colocalizes with the phosphoprotein. L is also shown to be phosphorylated by cellular kinases and to interact with the viral phosphoprotein in coimmunoprecipitation studies. These findings are consistent with the identity of the 190-kDa protein as the viral polymerase and provide insights and describe reagents that will be useful for Bornavirus molecular biology and pathobiology.


* Corresponding author. Mailing address: Emerging Diseases Laboratory, 3101 Gillespie Neuroscience Building, University of California, Irvine, CA 92697-4292. Phone: (949) 824-6193. Fax: (949) 824-1229. E-mail: ilipkin{at}uci.edu.


Journal of Virology, May 2000, p. 4425-4428, Vol. 74, No. 9
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Schneider, U., Blechschmidt, K., Schwemmle, M., Staeheli, P. (2004). Overlap of Interaction Domains Indicates a Central Role of the P Protein in Assembly and Regulation of the Borna Disease Virus Polymerase Complex. J. Biol. Chem. 279: 55290-55296 [Abstract] [Full Text]  
  • Schneider, U., Naegele, M., Staeheli, P., Schwemmle, M. (2003). Active Borna Disease Virus Polymerase Complex Requires a Distinct Nucleoprotein-to-Phosphoprotein Ratio but No Viral X Protein. J. Virol. 77: 11781-11789 [Abstract] [Full Text]  
  • Kobayashi, T., Zhang, G., Lee, B.-J., Baba, S., Yamashita, M., Kamitani, W., Yanai, H., Tomonaga, K., Ikuta, K. (2003). Modulation of Borna Disease Virus Phosphoprotein Nuclear Localization by the Viral Protein X Encoded in the Overlapping Open Reading Frame. J. Virol. 77: 8099-8107 [Abstract] [Full Text]  
  • Nishino, Y., Kobasa, D., Rubin, S. A., Pletnikov, M. V., Carbone, K. M. (2002). Enhanced Neurovirulence of Borna Disease Virus Variants Associated with Nucleotide Changes in the Glycoprotein and L Polymerase Genes. J. Virol. 76: 8650-8658 [Abstract] [Full Text]  
  • Walker, M. P., Lipkin, W. I. (2002). Characterization of the Nuclear Localization Signal of the Borna Disease Virus Polymerase. J. Virol. 76: 8460-8467 [Abstract] [Full Text]  
  • Kraus, I., Eickmann, M., Kiermayer, S., Scheffczik, H., Fluess, M., Richt, J. A., Garten, W. (2001). Open Reading Frame III of Borna Disease Virus Encodes a Nonglycosylated Matrix Protein. J. Virol. 75: 12098-12104 [Abstract] [Full Text]  
  • Pleschka, S., Staeheli, P., Kolodziejek, J., Richt, J. A., Nowotny, N., Schwemmle, M. (2001). Conservation of coding potential and terminal sequences in four different isolates of Borna disease virus. J. Gen. Virol. 82: 2681-2690 [Abstract] [Full Text]  
  • Carbone, K. M. (2001). Borna Disease Virus and Human Disease. Clin. Microbiol. Rev. 14: 513-527 [Abstract] [Full Text]  
  • Planz, O., Pleschka, S., Ludwig, S. (2001). MEK-Specific Inhibitor U0126 Blocks Spread of Borna Disease Virus in Cultured Cells. J. Virol. 75: 4871-4877 [Abstract] [Full Text]  
  • Kobayashi, T., Kamitani, W., Zhang, G., Watanabe, M., Tomonaga, K., Ikuta, K. (2001). Borna Disease Virus Nucleoprotein Requires both Nuclear Localization and Export Activities for Viral Nucleocytoplasmic Shuttling. J. Virol. 75: 3404-3412 [Abstract] [Full Text]  
  • Cubitt, B., Ly, C., de la Torre, J. C. (2001). Identification and characterization of a new intron in Borna disease virus. J. Gen. Virol. 82: 641-646 [Abstract] [Full Text]  
  • Tomonaga, K., Kobayashi, T., Lee, B. J., Watanabe, M., Kamitani, W., Ikuta, K. (2000). Identification of alternative splicing and negative splicing activity of a nonsegmented negative-strand RNA virus, Borna disease virus. Proc. Natl. Acad. Sci. USA 97: 12788-12793 [Abstract] [Full Text]