Closed circular viral DNA and asymmetrical heterogeneous forms in livers from animals infected with ground squirrel hepatitis virus

To identify possible intermediates in the replication of ground squirrel hepatitis virus, we characterized the major forms of intracellular virus-specific DNA in the livers of infected ground squirrels. A variety of DNA species were found: covalently closed circular molecules, relaxed circular molecules, and a heterogeneous collection of molecules that migrated ahead of closed circular DNA during agarose gel electrophoresis. The heterogeneous DNA was at least partly single stranded, consisted of minus strands in a greater than eight-fold mass excess of plus strands, and was tightly associated with protein.

[1]  J. Taylor,et al.  Protein covalently bound to minus-strand DNA intermediates of duck hepatitis B virus , 1983, Journal of virology.

[2]  Harold E. Varmus,et al.  Many tumors induced by the mouse mammary tumor virus contain a provirus integrated in the same region of the host genome , 1982, Cell.

[3]  H. Varmus,et al.  Biological characterization of acute infection with ground squirrel hepatitis virus , 1982, Journal of virology.

[4]  H. Varmus,et al.  Virion DNA of ground squirrel hepatitis virus: structural analysis and molecular cloning , 1982, Journal of virology.

[5]  J. Taylor,et al.  Asymmetric replication of duck hepatitis B virus DNA in liver cells: Free minus-strand DNA. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[6]  J. Summers,et al.  Replication of the genome of a hepatitis B-like virus by reverse transcription of an RNA intermediate , 1982, Cell.

[7]  D. Shafritz,et al.  Evidence for supercoiled hepatitis B virus DNA in chimpanzee liver and serum dane particles: Possible implications in persistent HBV infection , 1982, Cell.

[8]  E. Wimmer Genome-linked proteins of viruses , 1982, Cell.

[9]  H. Varmus,et al.  Analysis of avian leukosis virus DNA and RNA in bursal tumors: Viral gene expression is not required for maintenance of the tumor state , 1981, Cell.

[10]  J Messing,et al.  A system for shotgun DNA sequencing. , 1981, Nucleic acids research.

[11]  J. Summers,et al.  Virus of Pekin ducks with structural and biological relatedness to human hepatitis B virus , 1980, Journal of virology.

[12]  P. Thomas,et al.  Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[13]  W. Rutter,et al.  THE NUCLEOTIDE SEQUENCE OF THE HEPATITIS B VIRAL GENOME AND THE IDENTIFICATION OF THE MAJOR VIRAL GENES , 1980 .

[14]  H. Varmus,et al.  Mapping unintegrated avian sarcoma virus DNA: Termini of linear DNA bear 300 nucleotides present once or twice in two species of circular DNA , 1978, Cell.

[15]  J. Summers,et al.  A virus similar to human hepatitis B virus associated with hepatitis and hepatoma in woodchucks. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[16]  H. Greenberg,et al.  Structure of Hepatitis B Dane Particle DNA and Nature of the Endogenous DNA Polymerase Reaction , 1977, Journal of virology.

[17]  J. Rubenstein,et al.  Structure of hepatitis B Dane particle DNA before and after the Dane particle DNA polymerase reaction , 1977, Journal of virology.

[18]  R. Greenman,et al.  DNA of a Human Hepatitis B Virus Candidate , 1974, Journal of virology.

[19]  L. Grossman,et al.  Restricted uptake of ethidium bromide and propidium diiodide by denatured closed circular DNA in buoyant cesium chloride. , 1974, Journal of molecular biology.

[20]  R. Greenman,et al.  DNA Polymerase Associated with Human Hepatitis B Antigen , 1973, Journal of virology.