Literature DB >> 14694095

cis-Acting sequences that contribute to the synthesis of relaxed-circular DNA of human hepatitis B virus.

Ning Liu1, Lin Ji, Megan L Maguire, Daniel D Loeb.   

Abstract

Synthesis of the relaxed-circular (RC) genome of hepadnaviruses is a multistep process that requires template switching during reverse transcription. Studies of duck hepatitis B virus indicated the presence of cis-acting sequences, distinct from the donor and acceptor sequences for the template switches, which contribute to the synthesis of RC DNA. However, knowledge about cis-acting requirements distinct from the donor and acceptor sites for human hepatitis B virus (HBV) was lacking. In this study, we searched for cis-acting sequences for synthesis of HBV RC DNA by analyzing a set of deletion variants that collectively represent most of the HBV genome. Sequences of epsilon, DR1, DR2, 5'r, and 3'r were not analyzed in the study. Results from Southern blotting showed that multiple cis-acting sequences were involved in the synthesis of HBV RC DNA. Analysis of several HBV/woodchuck hepatitis virus chimeras corroborated the findings from the analysis of deletion variants. This study represents a comprehensive and quantitative analysis of cis-acting sequences that contribute to the synthesis of HBV RC DNA.

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Year:  2004        PMID: 14694095      PMCID: PMC368859          DOI: 10.1128/jvi.78.2.642-649.2004

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  35 in total

1.  The reverse transcriptase of hepatitis B virus acts as a protein primer for viral DNA synthesis.

Authors:  G H Wang; C Seeger
Journal:  Cell       Date:  1992-11-13       Impact factor: 41.582

2.  Novel mechanism for reverse transcription in hepatitis B viruses.

Authors:  G H Wang; C Seeger
Journal:  J Virol       Date:  1993-11       Impact factor: 5.103

3.  A bulged region of the hepatitis B virus RNA encapsidation signal contains the replication origin for discontinuous first-strand DNA synthesis.

Authors:  M Nassal; A Rieger
Journal:  J Virol       Date:  1996-05       Impact factor: 5.103

4.  Hepadnavirus reverse transcription initiates within the stem-loop of the RNA packaging signal and employs a novel strand transfer.

Authors:  J E Tavis; S Perri; D Ganem
Journal:  J Virol       Date:  1994-06       Impact factor: 5.103

5.  The P gene product of hepatitis B virus is required as a structural component for genomic RNA encapsidation.

Authors:  R Bartenschlager; M Junker-Niepmann; H Schaller
Journal:  J Virol       Date:  1990-11       Impact factor: 5.103

6.  The arginine-rich domain of the hepatitis B virus core protein is required for pregenome encapsidation and productive viral positive-strand DNA synthesis but not for virus assembly.

Authors:  M Nassal
Journal:  J Virol       Date:  1992-07       Impact factor: 5.103

7.  RNA sequences controlling the initiation and transfer of duck hepatitis B virus minus-strand DNA.

Authors:  J E Tavis; D Ganem
Journal:  J Virol       Date:  1995-07       Impact factor: 5.103

8.  Site-specific RNA binding by a hepatitis B virus reverse transcriptase initiates two distinct reactions: RNA packaging and DNA synthesis.

Authors:  J R Pollack; D Ganem
Journal:  J Virol       Date:  1994-09       Impact factor: 5.103

9.  A short cis-acting sequence is required for hepatitis B virus pregenome encapsidation and sufficient for packaging of foreign RNA.

Authors:  M Junker-Niepmann; R Bartenschlager; H Schaller
Journal:  EMBO J       Date:  1990-10       Impact factor: 11.598

10.  Hepadnaviral assembly is initiated by polymerase binding to the encapsidation signal in the viral RNA genome.

Authors:  R Bartenschlager; H Schaller
Journal:  EMBO J       Date:  1992-09       Impact factor: 11.598

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  18 in total

1.  cis-Acting sequences that contribute to synthesis of minus-strand DNA are not conserved between hepadnaviruses.

Authors:  Megan L Maguire; Daniel D Loeb
Journal:  J Virol       Date:  2010-10-06       Impact factor: 5.103

2.  Base pairing between the 5' half of epsilon and a cis-acting sequence, phi, makes a contribution to the synthesis of minus-strand DNA for human hepatitis B virus.

Authors:  Teresa M Abraham; Daniel D Loeb
Journal:  J Virol       Date:  2006-05       Impact factor: 5.103

Review 3.  Hepatitis B virus replication.

Authors:  Juergen Beck; Michael Nassal
Journal:  World J Gastroenterol       Date:  2007-01-07       Impact factor: 5.742

4.  Hepatitis B virus DNA replication is coordinated by core protein serine phosphorylation and HBx expression.

Authors:  Margherita Melegari; Sarah K Wolf; Robert J Schneider
Journal:  J Virol       Date:  2005-08       Impact factor: 5.103

5.  Base pairing between cis-acting sequences contributes to template switching during plus-strand DNA synthesis in human hepatitis B virus.

Authors:  Eric B Lewellyn; Daniel D Loeb
Journal:  J Virol       Date:  2007-04-04       Impact factor: 5.103

Review 6.  The evolution and clinical impact of hepatitis B virus genome diversity.

Authors:  Peter A Revill; Thomas Tu; Hans J Netter; Lilly K W Yuen; Stephen A Locarnini; Margaret Littlejohn
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2020-05-28       Impact factor: 46.802

7.  Hepatitis B Virus Polymerase Localizes to the Mitochondria, and Its Terminal Protein Domain Contains the Mitochondrial Targeting Signal.

Authors:  Nuruddin Unchwaniwala; Nathan M Sherer; Daniel D Loeb
Journal:  J Virol       Date:  2016-09-12       Impact factor: 5.103

8.  Encapsidated hepatitis B virus reverse transcriptase is poised on an ordered RNA lattice.

Authors:  Joseph Che-Yen Wang; David G Nickens; Thomas B Lentz; Daniel D Loeb; Adam Zlotnick
Journal:  Proc Natl Acad Sci U S A       Date:  2014-07-17       Impact factor: 11.205

9.  Three novel cis-acting elements required for efficient plus-strand DNA synthesis of the hepatitis B virus genome.

Authors:  Jehan Lee; Myeong-Kyun Shin; Hye-Jin Lee; Gyesoon Yoon; Wang-Shick Ryu
Journal:  J Virol       Date:  2004-07       Impact factor: 5.103

10.  Controllable inhibition of hepatitis B virus replication by a DR1-targeting short hairpin RNA (shRNA) expressed from a DOX-inducible lentiviral vector.

Authors:  Weiwei Wang; Hongquan Peng; Jiafu Li; Xiping Zhao; Fei Zhao; Kanghong Hu
Journal:  Virus Genes       Date:  2013-02-09       Impact factor: 2.332

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