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Journal of Virology, November 1998, p. 9116-9120, Vol. 72, No. 11
Department of Medicine II, University of
Freiburg, Freiburg, Germany
Received 1 June 1998/Accepted 6 August 1998
Hepadnaviruses are DNA viruses that replicate through reverse
transcription of an RNA pregenome. Viral DNA synthesis takes place
inside viral nucleocapsids, formed by core protein dimers. Previous
studies have identified carboxy-terminal truncations of the core
protein that affect viral DNA maturation. Here, we describe the effect
of small amino-terminal insertions into the duck hepatitis B virus
(DHBV) core protein on viral DNA replication. All insertion mutants
formed replication-competent nucleocapsids. Elongation of viral DNA,
however, appeared to be incomplete. Increasing the number of additional
amino acids and introducing negatively charged residues further
reduced the observed size of mature viral DNA species. Mutant core
proteins did not inhibit the viral polymerase. Instead, viral DNA
synthesis destabilized mutant nucleocapsids, rendering mature viral DNA
selectively sensitive to nuclease action. Interestingly, the phenotype
of two previously described carboxy-terminal DHBV core protein deletion
mutants was found to be based on the same mechanism. These data suggest
that (i) the amino- as well as the carboxy-terminal portion of the DHBV
core protein plays a critical role in nucleocapsid stabilization, and
(ii) the hepadnavirus polymerase can perform partial second-strand DNA
synthesis in the absence of intact viral nucleocapsids.
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Duck Hepatitis B Virus Nucleocapsids Formed by
N-Terminally Extended or C-Terminally Truncated Core Proteins
Disintegrate during Viral DNA Maturation

*
Corresponding author. Mailing address: Department of
Medicine II, University of Freiburg, Hugstetter Strasse 55, D-79106
Freiburg, Germany. Phone: 49-761-2703401. Fax: 49-761-2703610. E-mail:
weiz{at}ukl.uni-freiburg.de.
Present address: Molecular & Experimental Medicine, Scripps
Research Institute, La Jolla, CA 92037.
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