Literature DB >> 2352329

Resolution of poxvirus telomeres: processing of vaccinia virus concatemer junctions by conservative strand exchange.

M Merchlinsky1.   

Abstract

The replication of vaccinia virus proceeds through concatemeric intermediates which are resolved into unit-length DNA. In vaccinia virus-infected cells, plasmids containing the vaccinia virus DNA junction fragment that connects concatemers are resolved into linear minichromosomes of vector DNA flanked by hairpin loops. Resolution requires two copies of a specific nucleotide sequence conserved among poxviruses and found proximal to the hairpin loop. This study demonstrates that orientation of each sequence with respect to the other as well as to the axis of symmetry is critical for resolution, the processing of plasmids containing heterologous pairs of resolution sites is influenced by mismatched nucleotides between the sites, and the vaccinia virus hairpin in the linear minichromosome is a heteroduplex composed of DNA from each strand of the concatemer junction. A model incorporating site-specific recombination and orientated branch migration is proposed to account for resolution of the vaccinia virus concatemer junction.

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Year:  1990        PMID: 2352329      PMCID: PMC249602     

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


  61 in total

1.  G-strings at chromosome ends.

Authors:  T R Cech
Journal:  Nature       Date:  1988-04-28       Impact factor: 49.962

2.  Sequence-nonspecific replication of transfected plasmid DNA in poxvirus-infected cells.

Authors:  A M DeLange; G McFadden
Journal:  Proc Natl Acad Sci U S A       Date:  1986-02       Impact factor: 11.205

3.  Identification of temperature-sensitive mutants of vaccinia virus that are defective in conversion of concatemeric replicative intermediates to the mature linear DNA genome.

Authors:  A M DeLange
Journal:  J Virol       Date:  1989-06       Impact factor: 5.103

4.  Specific recognition of cruciform DNA by nuclear protein HMG1.

Authors:  M E Bianchi; M Beltrame; G Paonessa
Journal:  Science       Date:  1989-02-24       Impact factor: 47.728

5.  Multiple DNA-protein interactions governing high-precision DNA transactions.

Authors:  H Echols
Journal:  Science       Date:  1986-09-05       Impact factor: 47.728

6.  Characterization and localization of the naturally occurring cross-links in vaccinia virus DNA.

Authors:  P Geshelin; K I Berns
Journal:  J Mol Biol       Date:  1974-10-05       Impact factor: 5.469

7.  Dideoxy sequencing method using denatured plasmid templates.

Authors:  M Hattori; Y Sakaki
Journal:  Anal Biochem       Date:  1986-02-01       Impact factor: 3.365

8.  A vaccinia virus DNase preparation which cross-links superhelical DNA.

Authors:  N Lakritz; P D Foglesong; M Reddy; S Baum; J Hurwitz; W R Bauer
Journal:  J Virol       Date:  1985-03       Impact factor: 5.103

9.  Transposon-mediated site-specific recombination: a defined in vitro system.

Authors:  R R Reed
Journal:  Cell       Date:  1981-09       Impact factor: 41.582

10.  Isolation and characterization of the Tn3 resolvase synaptic intermediate.

Authors:  H W Benjamin; N R Cozzarelli
Journal:  EMBO J       Date:  1988-06       Impact factor: 11.598

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  10 in total

1.  In vitro resolution of poxvirus replicative intermediates into linear minichromosomes with hairpin termini by a virally induced Holliday junction endonuclease.

Authors:  D Stuart; K Ellison; K Graham; G McFadden
Journal:  J Virol       Date:  1992-03       Impact factor: 5.103

2.  The target DNA sequence for resolution of poxvirus replicative intermediates is an active late promoter.

Authors:  D Stuart; K Graham; M Schreiber; C Macaulay; G McFadden
Journal:  J Virol       Date:  1991-01       Impact factor: 5.103

3.  Mutational analysis of the resolution sequence of vaccinia virus DNA: essential sequence consists of two separate AT-rich regions highly conserved among poxviruses.

Authors:  M Merchlinsky
Journal:  J Virol       Date:  1990-10       Impact factor: 5.103

Review 4.  The vaccinia virus DNA polymerase and its processivity factor.

Authors:  Maciej W Czarnecki; Paula Traktman
Journal:  Virus Res       Date:  2017-02-01       Impact factor: 3.303

5.  Vaccinia virus nicking-joining enzyme is encoded by K4L (VACWR035).

Authors:  Dawn Eckert; Ollie Williams; Clement A Meseda; Michael Merchlinsky
Journal:  J Virol       Date:  2005-12       Impact factor: 5.103

6.  Resolution of a Holliday junction by vaccinia topoisomerase requires a spacer DNA segment 3' of the CCCTT/ cleavage sites.

Authors:  J Sekiguchi; C Cheng; S Shuman
Journal:  Nucleic Acids Res       Date:  2000-07-15       Impact factor: 16.971

7.  Resolution of Holliday junctions by eukaryotic DNA topoisomerase I.

Authors:  J Sekiguchi; N C Seeman; S Shuman
Journal:  Proc Natl Acad Sci U S A       Date:  1996-01-23       Impact factor: 11.205

8.  Characterization of the terminal inverted repeats and their neighboring tandem repeats in the Chlorella CVK1 virus genome.

Authors:  T Yamada; T Higashiyama
Journal:  Mol Gen Genet       Date:  1993-12

9.  Sgs1 RecQ helicase inhibits survival of Saccharomyces cerevisiae cells lacking telomerase and homologous recombination.

Authors:  Julia Y Lee; Jonathan L Mogen; Alejandro Chavez; F Brad Johnson
Journal:  J Biol Chem       Date:  2008-08-29       Impact factor: 5.157

10.  Origin-independent plasmid replication occurs in vaccinia virus cytoplasmic factories and requires all five known poxvirus replication factors.

Authors:  Frank S De Silva; Bernard Moss
Journal:  Virol J       Date:  2005-03-22       Impact factor: 4.099

  10 in total

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