Literature DB >> 10775628

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

M A McVoy1, D Ramnarain.   

Abstract

In many herpesviruses, genome segments flanked by inverted repeats invert during DNA replication. It is not known whether this inversion is a consequence of an inherently recombinagenic replicative mechanism common to all herpesviruses or whether the replication enzymes of viruses with invertible segments have specifically evolved additional enzymatic activities to drive inversion. By artificially inserting a fusion of terminal sequences into the genome of a virus which normally lacks invertible elements (murine cytomegalovirus), we created a genome composed of long and short segments flanked by 1,359- and 543-bp inverted repeats. Analysis of genomic DNA from this virus revealed that inversion of both segments generates equimolar amounts of four isomers during the viral propagation necessary to produce DNA for analysis from a single viral particle. We conclude that a herpesvirus which naturally lacks invertible elements is able to support efficient segment inversion. Thus, the potential to invert is probably inherent in the replication machinery of all herpesviruses, irrespective of genome structure, and therefore genomes with invertible elements could have evolved simply by acquisition of inverted repeats and without concomitant evolution of enzymatic activities to mediate inversion. Furthermore, the recombinagenicity of herpesvirus DNA replication must have some importance independent of genome segment inversion.

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Year:  2000        PMID: 10775628      PMCID: PMC112012          DOI: 10.1128/jvi.74.10.4882-4887.2000

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


  66 in total

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Authors:  R Martinez; R T Sarisky; P C Weber; S K Weller
Journal:  J Virol       Date:  1996-04       Impact factor: 5.103

2.  Herpes simplex virus replicative concatemers contain L components in inverted orientation.

Authors:  D Bataille; A Epstein
Journal:  Virology       Date:  1994-09       Impact factor: 3.616

3.  Genes in the HindIII J fragment of the murine cytomegalovirus genome are dispensable for growth in cultured cells: insertion mutagenesis with a lacZ/gpt cassette.

Authors:  J Vieira; H E Farrell; W D Rawlinson; E S Mocarski
Journal:  J Virol       Date:  1994-08       Impact factor: 5.103

4.  Characterization of ICP6::lacZ insertion mutants of the UL15 gene of herpes simplex virus type 1 reveals the translation of two proteins.

Authors:  D Yu; A K Sheaffer; D J Tenney; S K Weller
Journal:  J Virol       Date:  1997-04       Impact factor: 5.103

5.  The a sequence is dispensable for isomerization of the herpes simplex virus type 1 genome.

Authors:  D W Martin; P C Weber
Journal:  J Virol       Date:  1996-12       Impact factor: 5.103

6.  Analysis of the complete DNA sequence of murine cytomegalovirus.

Authors:  W D Rawlinson; H E Farrell; B G Barrell
Journal:  J Virol       Date:  1996-12       Impact factor: 5.103

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

Authors:  B Slobedman; A Simmons
Journal:  Virology       Date:  1997-03-17       Impact factor: 3.616

8.  The herpes simplex virus type 1 UL6 protein is essential for cleavage and packaging but not for genomic inversion.

Authors:  C Lamberti; S K Weller
Journal:  Virology       Date:  1996-12-15       Impact factor: 3.616

9.  Herpes simplex virus type 1 DNA replication is specifically required for high-frequency homologous recombination between repeated sequences.

Authors:  R E Dutch; V Bianchi; I R Lehman
Journal:  J Virol       Date:  1995-05       Impact factor: 5.103

10.  Peripheral blood mononuclear phagocytes mediate dissemination of murine cytomegalovirus.

Authors:  C A Stoddart; R D Cardin; J M Boname; W C Manning; G B Abenes; E S Mocarski
Journal:  J Virol       Date:  1994-10       Impact factor: 5.103

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  7 in total

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Journal:  J Virol       Date:  2001-07       Impact factor: 5.103

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4.  The impact of genome length on replication and genome stability of the herpesvirus guinea pig cytomegalovirus.

Authors:  Xiaohong Cui; Alistair McGregor; Mark R Schleiss; Michael A McVoy
Journal:  Virology       Date:  2009-01-26       Impact factor: 3.616

5.  Red-mediated transposition and final release of the mini-F vector of a cloned infectious herpesvirus genome.

Authors:  Felix Wussow; Helmut Fickenscher; B Karsten Tischer
Journal:  PLoS One       Date:  2009-12-04       Impact factor: 3.240

6.  Genome Sequencing of the Behavior Manipulating Virus LbFV Reveals a Possible New Virus Family.

Authors:  David Lepetit; Benjamin Gillet; Sandrine Hughes; Ken Kraaijeveld; Julien Varaldi
Journal:  Genome Biol Evol       Date:  2016-12-01       Impact factor: 3.416

7.  Comparative Genomics of Herpesviridae Family to Look for Potential Signatures of Human Infecting Strains.

Authors:  Vikas Sharma; Fauzul Mobeen; Tulika Prakash
Journal:  Int J Genomics       Date:  2016-05-26       Impact factor: 2.326

  7 in total

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