Abstract
PLC/PRF/5, a tissue culture cell line isolated from a human hepatocellular carcinoma and producing hepatitis B surface antigen, was studied for the presence of hepatitis B virus (HBV)-specific DNA and RNA. PLC/PRF/5 cell DNA accelerated the rate of reassociation of HBV [32P]DNA, and quantitative experiments indicated that the cells contained approximately four copies of viral DNA per haploid, mammalian cell DNA equivalent. PLC/PRF/5 DNA accelerated the rate of reassociation of all individual restriction endonucleases HincII and HaeIII fragments of HBV [32P]DNA, indicating that DNA from all regions of the viral genome is present in the cells. This suggests that these cells contain at least most, and possibly all, of the viral genome. Digestion of PLC/PRF/5 cell DNA with restriction endonuclease HindIII (an enzyme found not to cleave the DNA of any HBV isolate so far examined) yielded only three fragments, all larger than virion DNA, which contained HBV DNA base sequences, suggesting that HBV DNA is integrated in high-molecular-weight DNA at three different sites in these cells and that there is no viral DNA in an episomal form. PLC/PRF/5 cell [32P]RNA was found to hybridize with all restriction fragments of HBV DNA adequately tested, indicating that at least most, and possibly all, of the viral DNA in these cells is transcribed.
MeSH Terms
Base Sequence
Carcinoma, Hepatocellular/immunology,microbiology
Cell Line
DNA, Neoplasm/analysis
DNA, Viral/isolation & purification
Hepatitis B Surface Antigens/analysis
Hepatitis B virus/genetics
Humans
Liver Neoplasms/immunology,microbiology
Nucleic Acid Hybridization
RNA, Viral/analysis
Recombination, Genetic
Chemicals
DNA, Neoplasm
DNA, Viral
Hepatitis B Surface Antigens
RNA, Viral
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Marion P L
Salazar F H
Alexander J J
Robinson W S
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