» Articles » PMID: 2542582

Nucleotide Sequences at Recombinational Junctions Present in Pseudorabies Virus Variants with an Invertible L Component

Overview
Journal J Virol
Date 1989 Jun 1
PMID 2542582
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

The genome of pseudorabies virus (PrV) consists of two components--a noninvertible long (L) and an invertible short (S) component. The S component is bracketed by inverted repeats. In some variant strains of PrV (which have a selective growth advantage in certain cell lines), a sequence normally present at the left end of the L component has been translocated to the right end of the L component next to the inverted repeat. Consequently, these strains have acquired a genome with an L component that is bracketed by inverted repeats and that also inverts. We have determined the restriction maps and have analyzed the nucleotide sequences of those parts of the genome of three strains with invertible L components that contain the translocated segment of DNA. The results were as follows. The translocated fragments were derived in all cases from the extreme left end of the L component only. The sizes of the translocated fragments were similar, ranging from 1.3 to 1.4 kilobase pairs. The junction between the L and S components in these strains was the same as that in standard viral concatemeric DNA. The translocation of sequences from the left end of the genome next to the inverted repeats was always accompanied by a deletion of sequences from the right end of the L component. The sizes of the deleted fragments varied considerably, ranging from 0.8 to 2.3 kilobase pairs. Sequence homology at the points of recombination, i.e., at the junction between the right end and the left end of the L component, existed sometimes but not always. A model depicting how a virus with a class 2 genome (such as PrV) may acquire a genome with characteristics of a class 3 genome (such as herpes simplex virus) is presented.

Citing Articles

Assembly of pseudorabies virus genome-based transfer vehicle carrying major antigen sites of S gene of transmissible gastroenteritis virus: potential perspective for developing live vector vaccines.

Yin J, Ren X, Tian Z, Li Y Biologicals. 2006; 35(1):55-61.

PMID: 16731004 PMC: 7128284. DOI: 10.1016/j.biologicals.2006.02.001.


New nucleotide sequence data on the EMBL File Server.

Nucleic Acids Res. 1989; 17(18):7553-78.

PMID: 2798119 PMC: 334862. DOI: 10.1093/nar/17.18.7553.


Structural organization of the termini of the L and S components of the genome of pseudorabies virus.

DeMarchi J, Lu Z, Rall G, Kupershmidt S, Ben-Porat T J Virol. 1990; 64(10):4968-77.

PMID: 2168980 PMC: 247988. DOI: 10.1128/JVI.64.10.4968-4977.1990.


The three major immediate-early transcripts of bovine herpesvirus 1 arise from two divergent and spliced transcription units.

Wirth U, Vogt B, SCHWYZER M J Virol. 1991; 65(1):195-205.

PMID: 1845884 PMC: 240505. DOI: 10.1128/JVI.65.1.195-205.1991.


Acquisition of an additional internal cleavage site differentially affects the ability of pseudorabies virus to multiply in different host cells.

Rall G, Lu Z, Sugg N, Veach R, Ben-Porat T J Virol. 1991; 65(12):6604-11.

PMID: 1658364 PMC: 250723. DOI: 10.1128/JVI.65.12.6604-6611.1991.


References
1.
Ben-Porat T, DeMarchi J, Kaplan A . Characterization of defective interfering viral particles present in a population of pseudorabies virions. Virology. 1974; 61(1):29-37. DOI: 10.1016/0042-6822(74)90239-6. View

2.
Eagle H . Amino acid metabolism in mammalian cell cultures. Science. 1959; 130(3373):432-7. DOI: 10.1126/science.130.3373.432. View

3.
Southern E . Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975; 98(3):503-17. DOI: 10.1016/s0022-2836(75)80083-0. View

4.
Stevely W . Inverted repetition in the chromosome of pseudorabies virus. J Virol. 1977; 22(1):232-4. PMC: 515705. DOI: 10.1128/JVI.22.1.232-234.1977. View

5.
Rigby P, Dieckmann M, Rhodes C, Berg P . Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. J Mol Biol. 1977; 113(1):237-51. DOI: 10.1016/0022-2836(77)90052-3. View