Literature DB >> 6088785

Herpes simplex virus amplicon: effect of size on replication of constructed defective genomes containing eucaryotic DNA sequences.

A D Kwong, N Frenkel.   

Abstract

Previous studies (R. R. Spaete and N. Frenkel, Cell 30:295-304, 1982) have documented the potential use of defective virus vectors (amplicons) derived from herpes simplex virus for the efficient introduction of foreign DNA sequences into eucaryotic cells. Specifically, cotransfection of cells with helper virus DNA and cloned amplicons (8 to 10 kilobases [kb]) containing bacterial plasmid DNA sequences linked to a set of herpes simplex virus cis-acting propagation signals (a replication origin and a cleavage-packaging signal) resulted in the generation of virus stocks containing packaged defective genomes that consisted of uniform head-to-tail reiterations of the chimeric seed amplicon sequences. The chimeric defective genomes could be stably propagated in virus stocks and could thus be used to efficiently infect cells. We now report on additional studies designed to propagate relatively large sets of eucaryotic DNA sequences within chimeric packaged defective genomes. These studies have utilized a 12-kb chicken DNA sequence encoding the chicken ovalbumin gene and cloned by Lai et al. (Proc. Natl. Acad. Sci. U.S.A. 77:244-248, 1980) in the plasmid pOV12. Virus stocks derived from cells cotransfected with helper virus DNA and chimeric amplicons (overall size of 19.8 kb, of which 12 kb corresponded to the chicken DNA) contained defective genomes composed of reiterations of the 19.8-kb seed amplicon sequences. However, in addition to the authentically sized repeat units, defective genomes in the derivative virus stocks contained smaller repeat units representing deleted versions of the seed 19.8-kb amplicons. The recombinational events leading to the formation of deleted repeats did not appear to occur at unique sites, as shown by comparative analyses of multiple, independently generated virus series propagated from separate transfections. In contast, seed amplicons ranging in size from 11 to 15 kb and containing subsets of the 12-kb chicken DNA sequences replicated efficiently and could be stably propagated in virus stocks. The results of these studies suggest the existence of size restrictions (up to 15 kb) on the efficient replication of seed herpes simplex virus amplicons.

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Mesh:

Year:  1984        PMID: 6088785      PMCID: PMC255804     

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


  33 in total

1.  Site-specific inversion sequence of the herpes simplex virus genome: domain and structural features.

Authors:  E S Mocarski; B Roizman
Journal:  Proc Natl Acad Sci U S A       Date:  1981-11       Impact factor: 11.205

2.  Complete nucleotide sequence of the chicken chromosomal ovalbumin gene and its biological significance.

Authors:  S L Woo; W G Beattie; J F Catterall; A Dugaiczyk; R Staden; G G Brownlee; B W O'Malley
Journal:  Biochemistry       Date:  1981-10-27       Impact factor: 3.162

3.  The herpes simplex virus amplicon: a new eucaryotic defective-virus cloning-amplifying vector.

Authors:  R R Spaete; N Frenkel
Journal:  Cell       Date:  1982-08       Impact factor: 41.582

4.  Structure and expression of class II defective herpes simplex virus genomes encoding infected cell polypeptide number 8.

Authors:  H Locker; N Frenkel; I Halliburton
Journal:  J Virol       Date:  1982-08       Impact factor: 5.103

5.  Site-specific cleavage/packaging of herpes simplex virus DNA and the selective maturation of nucleocapsids containing full-length viral DNA.

Authors:  D A Vlazny; A Kwong; N Frenkel
Journal:  Proc Natl Acad Sci U S A       Date:  1982-03       Impact factor: 11.205

6.  The ovalbumin gene is associated with the nuclear matrix of chicken oviduct cells.

Authors:  S I Robinson; B D Nelkin; B Vogelstein
Journal:  Cell       Date:  1982-01       Impact factor: 41.582

7.  Differential hormonal responsiveness of the ovalbumin gene and its pseudogenes in the chick oviduct.

Authors:  D A Colbert; B J Knoll; S L Woo; M L Mace; M J Tsai; B W O'Malley
Journal:  Biochemistry       Date:  1980-11-25       Impact factor: 3.162

8.  Multiple structural features are responsible for the nuclease sensitivity of the active ovalbumin gene.

Authors:  A W Senear; R D Palmiter
Journal:  J Biol Chem       Date:  1981-02-10       Impact factor: 5.157

9.  Chicken oviduct progesterone receptor: location of specific regions of high-affinity binding in cloned DNA fragments of hormone-responsive genes.

Authors:  E R Mulvihill; J P LePennec; P Chambon
Journal:  Cell       Date:  1982-03       Impact factor: 41.582

10.  Replication of herpes simplex virus DNA: localization of replication recognition signals within defective virus genomes.

Authors:  D A Vlazny; N Frenkel
Journal:  Proc Natl Acad Sci U S A       Date:  1981-02       Impact factor: 11.205

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  16 in total

Review 1.  Virus-based gene delivery systems.

Authors:  Cathryn Mah; Barry J Byrne; Terence R Flotte
Journal:  Clin Pharmacokinet       Date:  2002       Impact factor: 6.447

2.  Transduction of human trophoblastic cells by replication-deficient recombinant viral vectors. Promoting cellular differentiation affects virus entry.

Authors:  S Parry; J Holder; M W Halterman; M D Weitzman; A R Davis; H Federoff; J F Strauss
Journal:  Am J Pathol       Date:  1998-06       Impact factor: 4.307

Review 3.  Gene transfer into the nervous system.

Authors:  X O Breakefield; A I Geller
Journal:  Mol Neurobiol       Date:  1987       Impact factor: 5.590

4.  A noninverting genome of a viable herpes simplex virus 1: presence of head-to-tail linkages in packaged genomes and requirements for circularization after infection.

Authors:  K L Poffenberger; B Roizman
Journal:  J Virol       Date:  1985-02       Impact factor: 5.103

5.  Nucleotide sequence and structural features of a novel US-a junction present in a defective herpes simplex virus genome.

Authors:  E S Mocarski; L P Deiss; N Frenkel
Journal:  J Virol       Date:  1985-07       Impact factor: 5.103

Review 6.  The function of herpes simplex virus genes: a primer for genetic engineering of novel vectors.

Authors:  B Roizman
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-15       Impact factor: 11.205

7.  Preproenkephalin promoter yields region-specific and long-term expression in adult brain after direct in vivo gene transfer via a defective herpes simplex viral vector.

Authors:  M G Kaplitt; A D Kwong; S P Kleopoulos; C V Mobbs; S D Rabkin; D W Pfaff
Journal:  Proc Natl Acad Sci U S A       Date:  1994-09-13       Impact factor: 11.205

8.  Use of amplicon-6 vectors derived from human herpesvirus 6 for efficient expression of membrane-associated and -secreted proteins in T cells.

Authors:  Ronen Borenstein; Oded Singer; Adi Moseri; Niza Frenkel
Journal:  J Virol       Date:  2004-05       Impact factor: 5.103

9.  Cloning, sequencing, and functional analysis of a Marek's disease virus origin of DNA replication.

Authors:  H S Camp; P M Coussens; R F Silva
Journal:  J Virol       Date:  1991-11       Impact factor: 5.103

10.  Cell culture amplification of a defective Marek's disease virus.

Authors:  J K Carter; R F Silva
Journal:  Virus Genes       Date:  1990-09       Impact factor: 2.332

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