Literature DB >> 2824785

Cruciform extrusion in plasmids bearing the replicative intermediate configuration of a poxvirus telomere.

P Dickie1, A R Morgan, G McFadden.   

Abstract

The transition from lineform DNA to cruciform DNA (cruciformation) within the cloned telomere sequences of the Leporipoxvirus Shope fibroma virus (SFV) has been studied. The viral telomere sequences have been cloned in recombination-deficient Escherichia coli as a 322 base-pair, imperfect palindromic insert in pUC13. The inverted repeat configuration is equivalent to the arrangement of the telomere structures observed within viral DNA replicative intermediates. A major cruciform structure in the purified recombinant plasmid has been identified and mapped using, as probes, the enzymes AflII, nuclease S1 and bacteriophage T7 endonuclease I. It was extruded from the central axis of the cloned viral inverted repeat and, by unrestricted branch migration, attained a size commensurate with the superhelical density of the plasmid molecule at native superhelical densities. This major cruciform extrusion event was the only detectable duplex DNA perturbation, induced by negative superhelical torsion, in the insert viral sequences. No significant steady-state pool of extruded cruciform was identified in E. coli. However, the identification of a major deletion variant generated even in the recombination-deficient E. coli strain DB1256 (recA recBC sbcB) suggested that the cruciform may be extruded transiently in vivo. The lineform to cruciform transition has been further characterized in vitro using two-dimensional agarose gel electrophoresis. The transition was marked by a high energy of formation (delta Gf = 44 kcal/mol), and an apparently low activation energy that enabled facile transitions at physiological temperatures provided there was sufficient torsional energy. By comparing cruciformation in a series of related bidirectional central axis deletions of the telomeric insert, it has been concluded that the presence of extrahelical bases in the terminal hairpin structures contributes substantially to the high delta Gf value. Also, viral sequences flanking the extruded cruciform were shown to influence the measured delta Gf value. Several general features of poxvirus telomere structure that would be expected to influence the facility of cruciform extrusion are discussed along with the implications of the observed cruciform transition event on the replicative process of poxviruses in vivo.

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Year:  1987        PMID: 2824785     DOI: 10.1016/0022-2836(87)90031-3

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  14 in total

1.  Bacterial-type DNA holliday junction resolvases in eukaryotic viruses.

Authors:  A D Garcia; L Aravind; E V Koonin; B Moss
Journal:  Proc Natl Acad Sci U S A       Date:  2000-08-01       Impact factor: 11.205

2.  Repression of vaccinia virus Holliday junction resolvase inhibits processing of viral DNA into unit-length genomes.

Authors:  A D Garcia; B Moss
Journal:  J Virol       Date:  2001-07       Impact factor: 5.103

3.  In vivo resolution of circular plasmids containing concatemer junction fragments from minute virus of mice DNA and their subsequent replication as linear molecules.

Authors:  S F Cotmore; P Tattersall
Journal:  J Virol       Date:  1992-01       Impact factor: 5.103

4.  T7 endonuclease I resolves Holliday junctions formed in vitro by RecA protein.

Authors:  B Müller; C Jones; S C West
Journal:  Nucleic Acids Res       Date:  1990-10-11       Impact factor: 16.971

5.  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

Review 6.  Poxvirus DNA replication.

Authors:  Bernard Moss
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-09-01       Impact factor: 10.005

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

Authors:  M Merchlinsky
Journal:  J Virol       Date:  1990-07       Impact factor: 5.103

8.  Metal cofactors in the structure and activity of the fowlpox resolvase.

Authors:  Matthew J Culyba; Young Hwang; Jimmy Yan Hu; Nana Minkah; Karen E Ocwieja; Frederic D Bushman
Journal:  J Mol Biol       Date:  2010-04-07       Impact factor: 5.469

9.  Nucleotide sequence required for resolution of the concatemer junction of vaccinia virus DNA.

Authors:  M Merchlinsky; B Moss
Journal:  J Virol       Date:  1989-10       Impact factor: 5.103

10.  Mapping vaccinia virus DNA replication origins at nucleotide level by deep sequencing.

Authors:  Tatiana G Senkevich; Daniel Bruno; Craig Martens; Stephen F Porcella; Yuri I Wolf; Bernard Moss
Journal:  Proc Natl Acad Sci U S A       Date:  2015-08-18       Impact factor: 11.205

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