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Intervirology. 2011;54(6):316-25.

Replicative activity of hepatitis B virus is negatively associated with methylation of covalently closed circular DNA in advanced hepatitis B virus infection.

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제1저자 김진욱 · 교신저자 김진욱

PMID 21242658 DOI 10.1159/000321450 IF 1.8 소화기내과
소속 (1)
  1. Department of Medicine, Seoul National University Bundang Hospital, Seongnam, South Korea.kimjw@snubh.org

Abstract

OBJECTIVES The aim of this study was to examine the methylation status of intrahepatic hepatitis B virus (HBV) covalently closed circular DNA (cccDNA) and to elucidate the possible relationship between the cccDNA methylation and viral replicative activity in patients with HBV-related liver cirrhosis (HBV-LC).

METHODS The methylation status of HBV cccDNA was investigated by bisulfite sequencing in nonneoplastic tissues from 12 patients with HBV-LC who underwent surgical resection for combined hepatocellular carcinoma. Clinical, biochemical and virologic factors were evaluated with respect to the degrees of cccDNA methylation. We also examined the effect of methylation of cccDNA on viral transcription by an in vitro transcription assay.

RESULTS Variable degrees of CpG methylation were present in the HBV cccDNA from patients with HBV-LC. Old age, low serum HBV DNA levels and low virion productivity were significantly associated with elevated cccDNA methylation. Virion productivity of cccDNA was also lower in HepAD38 cells with a higher degree of cccDNA methylation. In vitro transcription assays showed that the transcriptional activity of HBV cccDNA was suppressed by increased methylation of cccDNA.

CONCLUSIONS Increased CpG methylation of cccDNA is associated with old age, low serum HBV DNA levels and suppressed replicative activity in HBV-LC.

Copyright © 2011 S. Karger AG, Basel.

그 밖의 정보
출판 형태
Journal Article, Research Support, Non-U.S. Gov't
저널
Intervirology · eISSN 1423-0100
전자 출판
2011-01-14
MeSH
Adult · Aged · Base Sequence · Cell Line · Chromatin Immunoprecipitation · CpG Islands · DNA (Cytosine-5-)-Methyltransferases / metabolism · DNA Methylation* · DNA Methyltransferase 3A · DNA, Circular / genetics / isolation & purification · DNA, Viral / genetics / metabolism · DNA-Binding Proteins / metabolism · Female · Gene Expression Regulation, Viral · Hepatitis B virus / physiology · Hepatitis B, Chronic / virology · Humans · Liver Cirrhosis / virology · Male · Methyl-CpG-Binding Protein 2 / metabolism · Middle Aged · Molecular Sequence Data · Protein Binding · Sequence Alignment · Transcription Factors / metabolism · Transcription, Genetic · Virus Replication*
Substances
DNA, Circular · DNA, Viral · DNA-Binding Proteins · DNMT3A protein, human · MBD1 protein, human · MECP2 protein, human · Methyl-CpG-Binding Protein 2 · Transcription Factors · DNA (Cytosine-5-)-Methyltransferases · DNA Methyltransferase 3A