Quantification of HBV Covalently Closed Circular DNA from Liver Tissue by Real-Time PCR
Scott Bowden, Kathy Merlock Jackson, Margaret Littlejohn, Stephen Locarnini
Abstract
Scott Bowden, Kathy Merlock Jackson, Margaret Littlejohn, Stephen Locarnini
Abstract
Hepadnaviruses utilize an unusual replication strategy. On infection, the partially double-stranded open circular genomic DNA is transported to the hepatocyte nucleus, where host-cell enzymes convert it to a relaxed circular fully double-stranded molecule. From this replicative form is generated a covalently closed circular (ccc) DNA, which associates with cellular histones to form a viral minichromosome ( 1 , 2 ). The HBV (hepatitis B virus) ccc DNA remains in the cell nucleus and serves as the transcriptional template for HBV-RNA production. These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
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Hepadnaviruses utilize an unusual replication strategy. On infection, the partially double-stranded open circular genomic DNA is transported to the hepatocyte nucleus, where host-cell enzymes convert it to a relaxed circular fully double-stranded molecule. From this replicative form is generated a covalently closed circular (ccc) DNA, which associates with cellular histones to form a viral minichromosome ( 1 , 2 ). The HBV (hepatitis B virus) ccc DNA remains in the cell nucleus and serves as the transcriptional template for HBV-RNA production. These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
Key concepts: cccDNA, Minichromosome, Circular DNA, DNA, Hepatitis B virus, Biology, Histone, RNA