Literature DB >> 3981148

Comparative sequence analysis of duck and human hepatitis B virus genomes.

R Sprengel, C Kuhn, H Will, H Schaller.   

Abstract

We have cloned and sequenced an infectious, functionally active genome of a duck hepatitis B virus (DHBV). It is 3,021 base pairs (bp) in length and shows little DNA sequence homology to the genome of human hepatitis B virus (HBV). However, the amino acid sequences of predicted viral gene products are similar between DHBV and HBV, and the genome organization present in DHBV reflects that of HBV. As in the mammalian virus the long minus strand of the DHBV genome encodes three long overlapping reading frames designated as P, S, and C. The fourth open reading frame, termed X, is absent in DHBV. A comparison with a sequence of a second DHBV isolate [Mandart et al, Journal of Virology 49:782-792, 1984] revealed a nucleotide sequence variation of 5.6% and confirmed the presented overall gene organization of DHBV.

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Year:  1985        PMID: 3981148     DOI: 10.1002/jmv.1890150402

Source DB:  PubMed          Journal:  J Med Virol        ISSN: 0146-6615            Impact factor:   2.327


  74 in total

1.  Small DNA hairpin negatively regulates in situ priming during duck hepatitis B virus reverse transcription.

Authors:  Jeffrey W Habig; Daniel D Loeb
Journal:  J Virol       Date:  2002-02       Impact factor: 5.103

2.  Mutations that increase in situ priming also decrease circularization for duck hepatitis B virus.

Authors:  D D Loeb; R Tian
Journal:  J Virol       Date:  2001-07       Impact factor: 5.103

3.  The majority of duck hepatitis B virus reverse transcriptase in cells is nonencapsidated and is bound to a cytoplasmic structure.

Authors:  E Yao; Y Gong; N Chen; J E Tavis
Journal:  J Virol       Date:  2000-09       Impact factor: 5.103

4.  Integration of hepadnavirus DNA in infected liver: evidence for a linear precursor.

Authors:  W Yang; J Summers
Journal:  J Virol       Date:  1999-12       Impact factor: 5.103

5.  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

6.  An essential arginine residue for initiation of protein-primed DNA replication.

Authors:  J C Hsieh; S K Yoo; J Ito
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

7.  A secondary structure that contains the 5' and 3' splice sites suppresses splicing of duck hepatitis B virus pregenomic RNA.

Authors:  Daniel D Loeb; Amanda A Mack; Ru Tian
Journal:  J Virol       Date:  2002-10       Impact factor: 5.103

8.  X gene-related sequences in the core gene of duck and heron hepatitis B viruses.

Authors:  M A Feitelson; R H Miller
Journal:  Proc Natl Acad Sci U S A       Date:  1988-08       Impact factor: 11.205

9.  Transfer of the minus strand of DNA during hepadnavirus replication is not invariable but prefers a specific location.

Authors:  D D Loeb; R Tian
Journal:  J Virol       Date:  1995-11       Impact factor: 5.103

10.  An RNA stem-loop structure directs hepatitis B virus genomic RNA encapsidation.

Authors:  J R Pollack; D Ganem
Journal:  J Virol       Date:  1993-06       Impact factor: 5.103

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