Literature DB >> 6327886

The genome structure of cowpox virus white pock variants.

L C Archard, M Mackett, D E Barnes, K R Dumbell.   

Abstract

A previous report described restriction endonuclease analysis of white pock variants of red cowpox virus and their characterization as deletion mutants lacking certain sequences including the repetition from one specific terminus of the wild-type genome. Further analysis has confirmed the terminal deletion but demonstrated that this is compensated at the site of deletion by the presence of an inverted duplication of a variable amount of sequence from the opposite terminus, with the effect of restoring a terminal repetition and the covalent, terminal crosslink. Nine of 11 white pock variants showed a similar deletion of about 21 Mdal mapping contiguously from the right-hand terminus and extending into a 2.4 Mdal restriction fragment. Two white variants showed larger deletions of about 24 and 27 Mdal respectively. These deletions were compensated by a copy of sequences from the opposite terminus which ranged in size from 3 to 27 Mdal. No terminal deletions smaller than 21 Mdal were observed in cowpox white variants or in clones retaining the red phenotype. In contrast with other orthopoxviruses, no deletions involving the left-hand terminus were found. Some independent white isolates had similar sizes of sequence copied from the opposite terminus, but some sibling clones from a single, pock-purified white isolate with the same size of deletion had different sizes of duplicated sequence. Other siblings isolated from an independent, three times pock-purified white clone, itself derived from a single parental red pock, differed from each other in the size of both the deletion and the duplicated sequence. These observations suggest preference for deletion in a particular region, conjunction of the genome termini during DNA replication and a requirement for the preservation of symmetrical termini in orthopoxvirus genome function.

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Year:  1984        PMID: 6327886     DOI: 10.1099/0022-1317-65-5-875

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  14 in total

1.  An orthopoxvirus serpinlike gene controls the ability of infected cells to fuse.

Authors:  P C Turner; R W Moyer
Journal:  J Virol       Date:  1992-04       Impact factor: 5.103

2.  DNA sequence homology between the terminal inverted repeats of Shope fibroma virus and an endogenous cellular plasmid species.

Authors:  C Upton; G McFadden
Journal:  Mol Cell Biol       Date:  1986-01       Impact factor: 4.272

3.  Multigene families in African swine fever virus: family 360.

Authors:  A González; V Calvo; F Almazán; J M Almendral; J C Ramírez; I de la Vega; R Blasco; E Viñuela
Journal:  J Virol       Date:  1990-05       Impact factor: 5.103

4.  Localization and sequence of a vaccinia virus gene required for multiplication in human cells.

Authors:  S Gillard; D Spehner; R Drillien; A Kirn
Journal:  Proc Natl Acad Sci U S A       Date:  1986-08       Impact factor: 11.205

5.  The second-largest subunit of the poxvirus RNA polymerase is similar to the corresponding subunits of procaryotic and eucaryotic RNA polymerases.

Authors:  D D Patel; D J Pickup
Journal:  J Virol       Date:  1989-03       Impact factor: 5.103

6.  Spontaneous deletions and duplications of sequences in the genome of cowpox virus.

Authors:  D J Pickup; B S Ink; B L Parsons; W Hu; W K Joklik
Journal:  Proc Natl Acad Sci U S A       Date:  1984-11       Impact factor: 11.205

7.  Can variola-like viruses be derived from monkeypox virus? An investigation based on DNA mapping.

Authors:  J J Esposito; J H Nakano; J F Obijeski
Journal:  Bull World Health Organ       Date:  1985       Impact factor: 9.408

8.  Hemorrhage in lesions caused by cowpox virus is induced by a viral protein that is related to plasma protein inhibitors of serine proteases.

Authors:  D J Pickup; B S Ink; W Hu; C A Ray; W K Joklik
Journal:  Proc Natl Acad Sci U S A       Date:  1986-10       Impact factor: 11.205

9.  Interferon prevents the generation of spontaneous deletions at the left terminus of vaccinia virus DNA.

Authors:  E Paez; M Esteban
Journal:  J Virol       Date:  1985-10       Impact factor: 5.103

Review 10.  Poxvirus pathogenesis.

Authors:  R M Buller; G J Palumbo
Journal:  Microbiol Rev       Date:  1991-03
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