Literature DB >> 9126253

Concatemeric intermediates of equine herpesvirus type 1 DNA replication contain frequent inversions of adjacent long segments of the viral genome.

B Slobedman1, A Simmons.   

Abstract

In common with other alpha-herpesviruses, the genome of equine herpesvirus type-1 (EHV-1) comprises covalently linked long and short unique sequences of DNA, each flanked by inverted repeats. Equimolar amounts of two genomic isomers, generated by free inversion of the short segment, relative to the long segment, are packaged into EHV-1 virions. In contrast with herpes simplex virus (HSV), inversion of genomic long segments has not been described. In the current work, the structures of high molecular weight intermediates of EHV-1 DNA replication were studied by field inversion gel electrophoresis. It is shown that adjacent long segments of the viral genome are frequently inverted in concatemeric intermediates of EHV-1 DNA replication. Further, like HSV concatemers, high molecular weight intermediates of EHV-1 replication are flanked exclusively by the long segment of the viral genome. Hence, despite the fact that only two, rather than four, isomers of EHV-1 DNA are packaged into virions, the intermediates of EHV-1 DNA replication closely resemble those of herpes simplex virus type 1 in structure. These data have implications relating to the mechanisms involved in packaging of alpha-herpesvirus DNA.

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Year:  1997        PMID: 9126253     DOI: 10.1006/viro.1997.8447

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  9 in total

1.  Machinery to support genome segment inversion exists in a herpesvirus which does not naturally contain invertible elements.

Authors:  M A McVoy; D Ramnarain
Journal:  J Virol       Date:  2000-05       Impact factor: 5.103

2.  The ends on herpesvirus DNA replicative concatemers contain pac2 cis cleavage/packaging elements and their formation is controlled by terminal cis sequences.

Authors:  M A McVoy; D E Nixon; J K Hur; S P Adler
Journal:  J Virol       Date:  2000-02       Impact factor: 5.103

3.  Quantitative analysis of latent human cytomegalovirus.

Authors:  B Slobedman; E S Mocarski
Journal:  J Virol       Date:  1999-06       Impact factor: 5.103

4.  Effects of mutations within the herpes simplex virus type 1 DNA encapsidation signal on packaging efficiency.

Authors:  P D Hodge; N D Stow
Journal:  J Virol       Date:  2001-10       Impact factor: 5.103

5.  Sequences within the herpesvirus-conserved pac1 and pac2 motifs are required for cleavage and packaging of the murine cytomegalovirus genome.

Authors:  M A McVoy; D E Nixon; S P Adler; E S Mocarski
Journal:  J Virol       Date:  1998-01       Impact factor: 5.103

6.  The varicella-zoster virus ORFS/L (ORF0) gene is required for efficient viral replication and contains an element involved in DNA cleavage.

Authors:  Benedikt B Kaufer; Benjamin Smejkal; Nikolaus Osterrieder
Journal:  J Virol       Date:  2010-09-15       Impact factor: 5.103

7.  Packaging of genomic and amplicon DNA by the herpes simplex virus type 1 UL25-null mutant KUL25NS.

Authors:  N D Stow
Journal:  J Virol       Date:  2001-11       Impact factor: 5.103

8.  Polarized DNA ejection from the herpesvirus capsid.

Authors:  William W Newcomb; Shelley K Cockrell; Fred L Homa; Jay C Brown
Journal:  J Mol Biol       Date:  2009-07-23       Impact factor: 5.469

9.  Dramatic effects of 2-bromo-5,6-dichloro-1-beta-D-ribofuranosyl benzimidazole riboside on the genome structure, packaging, and egress of guinea pig cytomegalovirus.

Authors:  Daniel E Nixon; Michael A McVoy
Journal:  J Virol       Date:  2004-02       Impact factor: 5.103

  9 in total

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