Literature DB >> 221666

Structure and origin of defective genomes contained in serially passaged herpes simplex virus type 1 (Justin).

H Locker, N Frenkel.   

Abstract

Restriction enzyme and hybridization analyses have revealed that high-density DNA prepared from passage 15 of serially passaged herpes simplex virus type 1 (Justin) contains three major classes of modified viral DNA molecules, each composed of distinct but closely related types of repeate units. The DNA sequences within the three types of repeat units are colinear with the DNA sequences located at the right end (between coordinates 0.94 and 1.0) of the parental herpes simplex virus type 1 genome. Thus, the three types of repeat units each contain the entire repeat sequence (ac) (which brackets the unique sequences of the small [S] component of herpes simplex virus type 1 DNA) and differ only with respect to the amount of unique S sequences which they contain. The three classes of high-density DNA molecules were found to be stably propagated between passages 6 and 15 of this series.

Entities:  

Mesh:

Substances:

Year:  1979        PMID: 221666      PMCID: PMC353267     

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


  30 in total

1.  Inverted repetitions in the chromosome of herpes simplex virus.

Authors:  P Sheldrick; N Berthelot
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1975

2.  Analysis of DNA of defective herpes simplex virus type 1 by restriction endonuclease cleavage and nucleic acid hybridization.

Authors:  M Wagner; J Skare; W C Summers
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1975

3.  Anatomy of herpes simplex virus DNA. III. Characterization of defective DNA molecules and biological properties of virus populations containing them.

Authors:  N Frenkel; R J Jacob; R W Honess; G S Hayward; H Locker; B Roizman
Journal:  J Virol       Date:  1975-07       Impact factor: 5.103

4.  Anatomy of herpes simplex virus DNA. II. Size, composition, and arrangement of inverted terminal repetitions.

Authors:  S Wadsworth; R J Jacob; B Roizman
Journal:  J Virol       Date:  1975-06       Impact factor: 5.103

5.  Equine herpesvirus in vivo: cyclic production of a DNA density variant with repetitive sequences.

Authors:  D E Campbell; M C Kemp; M L Perdue; C C Randall; G A Gentry
Journal:  Virology       Date:  1976-02       Impact factor: 3.616

6.  Cyclic appearance of defective interfering particles of herpes simplex virus and the concomitant accumulation of early polypeptide VP175.

Authors:  B K Murray; N Biswal; J B Bookout; R E Lanford; R J Courtney; J L Melnick
Journal:  Intervirology       Date:  1975       Impact factor: 1.763

7.  A partial denaturation map of herpes simplex virus type 1 DNA: evidence for inversions of the unique DNA regions.

Authors:  H Delius; J B Clements
Journal:  J Gen Virol       Date:  1976-10       Impact factor: 3.891

8.  Anatomy of herpes simplex virus DNA: evidence for four populations of molecules that differ in the relative orientations of their long and short components.

Authors:  G S Hayward; R J Jacob; S C Wadsworth; B Roizman
Journal:  Proc Natl Acad Sci U S A       Date:  1975-11       Impact factor: 11.205

9.  Physical maps for Herpes simplex virus type 1 DNA for restriction endonucleases Hind III, Hpa-1, and X. bad.

Authors:  N M Wilkie
Journal:  J Virol       Date:  1976-10       Impact factor: 5.103

10.  Anatomy of herpes simplex virus DNA. VI. Defective DNA originates from the S component.

Authors:  N Frenkeĺ; H Locker; W Batterson; G S Hayward; B Roizman
Journal:  J Virol       Date:  1976-11       Impact factor: 5.103

View more
  27 in total

Review 1.  HSV-1-based vectors for gene therapy of neurological diseases and brain tumors: part II. Vector systems and applications.

Authors:  A Jacobs; X O Breakefield; C Fraefel
Journal:  Neoplasia       Date:  1999-11       Impact factor: 5.715

2.  A cellular function can enhance gene expression and plating efficiency of a mutant defective in the gene for ICP0, a transactivating protein of herpes simplex virus type 1.

Authors:  W Cai; P A Schaffer
Journal:  J Virol       Date:  1991-08       Impact factor: 5.103

3.  Cloning human herpes virus 6A genome into bacterial artificial chromosomes and study of DNA replication intermediates.

Authors:  Ronen Borenstein; Niza Frenkel
Journal:  Proc Natl Acad Sci U S A       Date:  2009-10-26       Impact factor: 11.205

4.  Isolation of novel herpes simplex virus type 1 derivatives with tandem duplications of DNA sequences encoding immediate-early mRNA-5 and an origin of replication.

Authors:  K Umene; L W Enquist
Journal:  J Virol       Date:  1985-02       Impact factor: 5.103

5.  Cloning, sequencing, and functional analysis of oriL, a herpes simplex virus type 1 origin of DNA synthesis.

Authors:  S K Weller; A Spadaro; J E Schaffer; A W Murray; A M Maxam; P A Schaffer
Journal:  Mol Cell Biol       Date:  1985-05       Impact factor: 4.272

6.  The alpha sequence of the cytomegalovirus genome functions as a cleavage/packaging signal for herpes simplex virus defective genomes.

Authors:  R R Spaete; E S Mocarski
Journal:  J Virol       Date:  1985-06       Impact factor: 5.103

7.  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

8.  Herpes simplex virus amplicon: cleavage of concatemeric DNA is linked to packaging and involves amplification of the terminally reiterated a sequence.

Authors:  L P Deiss; N Frenkel
Journal:  J Virol       Date:  1986-03       Impact factor: 5.103

9.  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

10.  The herpes simplex virus type 1 (HSV-1) a sequence serves as a cleavage/packaging signal but does not drive recombinational genome isomerization when it is inserted into the HSV-2 genome.

Authors:  J R Smiley; C Lavery; M Howes
Journal:  J Virol       Date:  1992-12       Impact factor: 5.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.