Literature DB >> 11581421

Isomerization of a uniquely designed amplicon during herpes simplex virus-mediated replication.

H Wang1, X Fu, X Zhang.   

Abstract

Herpes simplex virus (HSV) type 1 DNA isomerization was studied using a uniquely designed amplicon that mimics the viral genomic structure. The results revealed that amplicon concatemers frequently contain adjacent amplicon units with their segments in opposed orientations. These unusual concatemers were generated through homologous recombination, which does not require HSV DNA as the source of homology.

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Year:  2001        PMID： 11581421      PMCID： PMC114627          DOI： 10.1128/JVI.75.21.10505-10510.2001

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


  27 in total

1.  Anatomy of herpes simplex virus DNA VIII. Properties of the replicating DNA.

Authors:  R J Jacob; B Roizman
Journal:  J Virol       Date:  1977-08       Impact factor: 5.103

2.  Replication of herpesvirus DNA. II. Sedimentation characteristics of newly synthesized DNA.

Authors:  T Ben-Porat; S A Tokazewski
Journal:  Virology       Date:  1977-06-15       Impact factor: 3.616

3.  A noninverting genome of a viable herpes simplex virus 1: presence of head-to-tail linkages in packaged genomes and requirements for circularization after infection.

Authors:  K L Poffenberger; B Roizman
Journal:  J Virol       Date:  1985-02       Impact factor: 5.103

4.  Signals for site-specific cleavage of HSV DNA: maturation involves two separate cleavage events at sites distal to the recognition sequences.

Authors:  S L Varmuza; J R Smiley
Journal:  Cell       Date:  1985-07       Impact factor: 41.582

5.  Herpes simplex virus amplicon: cleavage of concatemeric DNA is linked to packaging and involves amplification of the terminally reiterated a sequence.

Authors:  L P Deiss; N Frenkel
Journal:  J Virol       Date:  1986-03       Impact factor: 5.103

6.  Site-specific inversion sequence of the herpes simplex virus genome: domain and structural features.

Authors:  E S Mocarski; B Roizman
Journal:  Proc Natl Acad Sci U S A       Date:  1981-11       Impact factor: 11.205

7.  Construction of a double-jointed herpes simplex viral DNA molecule: inverted repeats are required for segment inversion, and direct repeats promote deletions.

Authors:  J R Smiley; B S Fong; W C Leung
Journal:  Virology       Date:  1981-08       Impact factor: 3.616

8.  Molecular engineering of the herpes simplex virus genome: insertion of a second L-S junction into the genome causes additional genome inversions.

Authors:  E S Mocarski; L E Post; B Roizman
Journal:  Cell       Date:  1980-11       Impact factor: 41.582

9.  Herpesvirus-dependent amplification and inversion of cell-associated viral thymidine kinase gene flanked by viral a sequences and linked to an origin of viral DNA replication.

Authors:  E S Mocarski; B Roizman
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

10.  Site-specific cleavage/packaging of herpes simplex virus DNA and the selective maturation of nucleocapsids containing full-length viral DNA.

Authors:  D A Vlazny; A Kwong; N Frenkel
Journal:  Proc Natl Acad Sci U S A       Date:  1982-03       Impact factor: 11.205
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  1 in total

1.  High-frequency intermolecular homologous recombination during herpes simplex virus-mediated plasmid DNA replication.

Authors:  Xinping Fu; Hua Wang; Xiaoliu Zhang
Journal:  J Virol       Date:  2002-06       Impact factor: 5.103
  1 in total

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