Literature DB >> 8985334

Sequence identity of the terminal redundancies on the minus-strand DNA template is necessary but not sufficient for the template switch during hepadnavirus plus-strand DNA synthesis.

D D Loeb1, K J Gulya, R Tian.   

Abstract

The template for hepadnavirus plus-strand DNA synthesis is a terminally redundant minus-strand DNA. An intramolecular template switch during plus-strand DNA synthesis, which permits plus-strand DNA elongation, has been proposed to be facilitated by this terminal redundancy, which is 7 to 9 nucleotides long. The aim of this study was to determine whether the presence of identical copies of the redundancy on the minus-strand DNA template was necessary and/or sufficient for the template switch and at what position(s) within the redundancy the switch occurs for duck hepatitis B virus. When dinucleotide insertions were placed within the copy of the redundancy at the 3' end of the minus-strand DNA template, novel sequences were copied into plus-strand DNA. The generation of these novel sequences could be explained by complete copying of the redundancy at the 5' end of the minus-strand DNA template followed by a template switch and then extension from a mismatched 3' terminus. In a second set of experiments, it was found that when one copy of the redundancy had either three or five nucleotides replaced the template switch was inhibited. When the identical, albeit mutant, sequences were restored in both copies of the redundancy, template switching was not necessarily restored. Our results indicate that the terminal redundancy on the minus-strand DNA template is necessary but not sufficient for template switching.

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Year:  1997        PMID: 8985334      PMCID: PMC191035     

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


  20 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.  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

3.  Mechanism of release of the avian rotavirus tRNATrp primer molecule from viral DNA by ribonuclease H during reverse transcription.

Authors:  C A Omer; A J Faras
Journal:  Cell       Date:  1982-10       Impact factor: 41.582

4.  Protein covalently bound to minus-strand DNA intermediates of duck hepatitis B virus.

Authors:  K L Molnar-Kimber; J Summers; J M Taylor; W S Mason
Journal:  J Virol       Date:  1983-01       Impact factor: 5.103

5.  Hepatitis B virus contains protein attached to the 5' terminus of its complete DNA strand.

Authors:  W H Gerlich; W S Robinson
Journal:  Cell       Date:  1980-10       Impact factor: 41.582

6.  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

7.  Virion DNA of ground squirrel hepatitis virus: structural analysis and molecular cloning.

Authors:  D Ganem; L Greenbaum; H E Varmus
Journal:  J Virol       Date:  1982-10       Impact factor: 5.103

8.  Replication strategy of human hepatitis B virus.

Authors:  H Will; W Reiser; T Weimer; E Pfaff; M Büscher; R Sprengel; R Cattaneo; H Schaller
Journal:  J Virol       Date:  1987-03       Impact factor: 5.103

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

Authors:  R Sprengel; C Kuhn; H Will; H Schaller
Journal:  J Med Virol       Date:  1985-04       Impact factor: 2.327

10.  Biochemical and genetic evidence for the hepatitis B virus replication strategy.

Authors:  C Seeger; D Ganem; H E Varmus
Journal:  Science       Date:  1986-04-25       Impact factor: 47.728

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

Authors:  Ning Liu; Lin Ji; Megan L Maguire; Daniel D Loeb
Journal:  J Virol       Date:  2004-01       Impact factor: 5.103

4.  Base pairing among three cis-acting sequences contributes to template switching during hepadnavirus reverse transcription.

Authors:  Ning Liu; Ru Tian; Daniel D Loeb
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-10       Impact factor: 11.205

5.  A novel cis-acting element facilitates minus-strand DNA synthesis during reverse transcription of the hepatitis B virus genome.

Authors:  Myeong-Kyun Shin; Jehan Lee; Wang-Shick Ryu
Journal:  J Virol       Date:  2004-06       Impact factor: 5.103

6.  Identification of an essential molecular contact point on the duck hepatitis B virus reverse transcriptase.

Authors:  Feng Cao; Matthew P Badtke; Lisa M Metzger; Ermei Yao; Babatunde Adeyemo; Yunhao Gong; John E Tavis
Journal:  J Virol       Date:  2005-08       Impact factor: 5.103

7.  Insertions within epsilon affect synthesis of minus-strand DNA before the template switch for duck hepatitis B virus.

Authors:  H Jiang; D D Loeb
Journal:  J Virol       Date:  1997-07       Impact factor: 5.103

8.  cis-Acting sequences in addition to donor and acceptor sites are required for template switching during synthesis of plus-strand DNA for duck hepatitis B virus.

Authors:  M B Havert; D D Loeb
Journal:  J Virol       Date:  1997-07       Impact factor: 5.103

9.  Complementarity between epsilon and phi sequences in pregenomic RNA influences hepatitis B virus replication efficiency.

Authors:  Claudia E Oropeza; Alan McLachlan
Journal:  Virology       Date:  2006-10-23       Impact factor: 3.616

10.  Mechanism for CCC DNA synthesis in hepadnaviruses.

Authors:  Ji A Sohn; Samuel Litwin; Christoph Seeger
Journal:  PLoS One       Date:  2009-11-30       Impact factor: 3.240

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