Literature DB >> 8411359

Detection of DNA polymerase activities associated with purified duck hepatitis B virus core particles by using an activity gel assay.

S M Oberhaus1, J E Newbold.   

Abstract

Replication of hepadnaviruses involves reverse transcription of an intermediate RNA molecule. It is generally accepted that this replication scheme is carried out by a virally encoded, multifunctional polymerase which has DNA-dependent DNA polymerase, reverse transcriptase, and RNase H activities. Biochemical studies of the polymerase protein(s) have been limited by the inability to purify useful quantities of functional enzyme from virus particles and, until recently, to express enzymatically active polymerase proteins in heterologous systems. An activity gel assay which detects in situ catalytic activities of DNA polymerases after electrophoresis in partially denaturing polyacrylamide gels was used by M.R. Bavand and O. Laub (J. Virol. 62:626-628, 1988) to show the presence of DNA- and RNA-dependent DNA polymerase activities associated with hepatitis B virus particles produced in vitro. This assay has provided the only means by which hepadnavirus polymerase proteins have been detected in association with enzymatic activities. Since conventional methods have not allowed purification of useful quantities of enzymatically active polymerase protein(s), we have devised a protocol for purifying large quantities of duck hepatitis B virus (DHBV) core particles to near homogeneity. These immature virus particles contain DNA- and RNA-dependent DNA polymerase activities, as shown in the endogenous DNA polymerase assay. We have used the activity gel assay to detect multiple DNA- and RNA-dependent DNA polymerase proteins associated with these purified DHBV core particles. These enzymatically active proteins appear larger than, approximately the same size as, and smaller than an unmodified DHBV polymerase protein predicted from the polymerase open reading frame. This is the first report of the detection of active hepadnavirus core-associated DNA polymerase proteins derived from a natural host.

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Year:  1993        PMID: 8411359      PMCID: PMC238093     

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


  40 in total

1.  Evidence that a capped oligoribonucleotide is the primer for duck hepatitis B virus plus-strand DNA synthesis.

Authors:  J M Lien; C E Aldrich; W S Mason
Journal:  J Virol       Date:  1986-01       Impact factor: 5.103

2.  Expression of functional hepatitis B virus polymerase in yeast reveals it to be the sole viral protein required for correct initiation of reverse transcription.

Authors:  J E Tavis; D Ganem
Journal:  Proc Natl Acad Sci U S A       Date:  1993-05-01       Impact factor: 11.205

3.  Two proteins with reverse transcriptase activities associated with hepatitis B virus-like particles.

Authors:  M R Bavand; O Laub
Journal:  J Virol       Date:  1988-02       Impact factor: 5.103

4.  Hepatitis B virus particles contain a polypeptide encoded by the largest open reading frame: a putative reverse transcriptase.

Authors:  D H Mack; W Bloch; N Nath; J J Sninsky
Journal:  J Virol       Date:  1988-12       Impact factor: 5.103

5.  Initiation and termination of duck hepatitis B virus DNA synthesis during virus maturation.

Authors:  J M Lien; D J Petcu; C E Aldrich; W S Mason
Journal:  J Virol       Date:  1987-12       Impact factor: 5.103

6.  The duck hepatitis B virus DNA polymerase is tightly associated with the viral core structure and unable to switch to an exogenous template.

Authors:  G Radziwill; H Zentgraf; H Schaller; V Bosch
Journal:  Virology       Date:  1988-03       Impact factor: 3.616

7.  Formation of the pool of covalently closed circular viral DNA in hepadnavirus-infected cells.

Authors:  J S Tuttleman; C Pourcel; J Summers
Journal:  Cell       Date:  1986-11-07       Impact factor: 41.582

8.  Nucleotide sequence of a cloned duck hepatitis B virus genome: comparison with woodchuck and human hepatitis B virus sequences.

Authors:  E Mandart; A Kay; F Galibert
Journal:  J Virol       Date:  1984-03       Impact factor: 5.103

9.  The duck hepatitis B virus P-gene codes for protein strongly associated with the 5'-end of the viral DNA minus strand.

Authors:  V Bosch; R Bartenschlager; G Radziwill; H Schaller
Journal:  Virology       Date:  1988-10       Impact factor: 3.616

10.  Common evolutionary origin of hepatitis B virus and retroviruses.

Authors:  R H Miller; W S Robinson
Journal:  Proc Natl Acad Sci U S A       Date:  1986-04       Impact factor: 11.205

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  10 in total

1.  Duck hepatitis B virus virion secretion requires a double-stranded DNA genome.

Authors:  David Perlman; Jianming Hu
Journal:  J Virol       Date:  2003-02       Impact factor: 5.103

Review 2.  Hepatitis B virus biology.

Authors:  C Seeger; W S Mason
Journal:  Microbiol Mol Biol Rev       Date:  2000-03       Impact factor: 11.056

3.  Efficient pyrophosphorolysis by a hepatitis B virus polymerase may be a primer-unblocking mechanism.

Authors:  S Urban; S Urban; K P Fischer; D L Tyrrell
Journal:  Proc Natl Acad Sci U S A       Date:  2001-04-24       Impact factor: 11.205

4.  Generation of replication-competent hepatitis B virus nucleocapsids in insect cells.

Authors:  M Seifer; R Hamatake; M Bifano; D N Standring
Journal:  J Virol       Date:  1998-04       Impact factor: 5.103

5.  Selected mutations of the duck hepatitis B virus P gene RNase H domain affect both RNA packaging and priming of minus-strand DNA synthesis.

Authors:  Y Chen; W S Robinson; P L Marion
Journal:  J Virol       Date:  1994-08       Impact factor: 5.103

6.  Detection of an RNase H activity associated with hepadnaviruses.

Authors:  S M Oberhaus; J E Newbold
Journal:  J Virol       Date:  1995-09       Impact factor: 5.103

7.  Nucleotide priming and reverse transcriptase activity of hepatitis B virus polymerase expressed in insect cells.

Authors:  R E Lanford; L Notvall; B Beames
Journal:  J Virol       Date:  1995-07       Impact factor: 5.103

8.  The covalently closed duplex form of the hepadnavirus genome exists in situ as a heterogeneous population of viral minichromosomes.

Authors:  J E Newbold; H Xin; M Tencza; G Sherman; J Dean; S Bowden; S Locarnini
Journal:  J Virol       Date:  1995-06       Impact factor: 5.103

9.  Evidence that the RNAseH activity of the duck hepatitis B virus is unable to act on exogenous substrates.

Authors:  Y Gong; E Yao; J E Tavis
Journal:  BMC Microbiol       Date:  2001-07-19       Impact factor: 3.605

10.  Extracellular Hepatitis B Virus RNAs Are Heterogeneous in Length and Circulate as Capsid-Antibody Complexes in Addition to Virions in Chronic Hepatitis B Patients.

Authors:  Lu Bai; Xiaonan Zhang; Maya Kozlowski; Weixia Li; Min Wu; Jiangxia Liu; Liang Chen; Jiming Zhang; Yuxian Huang; Zhenghong Yuan
Journal:  J Virol       Date:  2018-11-27       Impact factor: 5.103

  10 in total

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