Literature DB >> 8207811

Excision of DNA fragments corresponding to the unit-length a sequence of herpes simplex virus type 1 and terminus variation predominate on one side of the excised fragment.

K Umene1.   

Abstract

DNA fragments corresponding to the unit-length a sequence of herpes simplex virus type 1 (HSV-1) were identified in HSV-1 DNA preparations extracted by the method of Hirt. The DNA fragments were molecularly cloned, and nucleotide sequences were determined. Most termini of the fragments were at sites on DR1 corresponding to the termini of linear HSV-1 DNA generated by the cleavage-packaging system. In one-step growth experiments, DNA fragments of the unit-length a sequence appeared simultaneously with the termini of linear HSV-1 DNAs produced by cleavage of circular and concatemeric DNAs. Therefore, excision of the unit-length a sequence appeared closely related to the cleavage-packaging system. Termini of the excised DNA fragments of the variant a sequence with two DR2 arrays varied on the L-component side, while termini on the S-component side were at the site on DR1 corresponding to the authentic cleavage site. It is thus assumed that the cleavage-packaging system functions adequately on the DR1 second distal from the S component, and cleavages of other DR1 are rare and less accurate. If this notion is tenable, then most termini on the S-component side of the excised DNA fragments are derived from the second DR1 properly cleaved and should be constant, while termini on the L-component side are from regions on and around the DR1 third distal from the S component and may be variable. Cleavage of DR1 is likely to be affected by the topological relationship with the S component.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8207811      PMCID: PMC236361     

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


  40 in total

1.  Characterization of DNA sequence-common and sequence-specific proteins binding to cis-acting sites for cleavage of the terminal a sequence of the herpes simplex virus 1 genome.

Authors:  J Chou; B Roizman
Journal:  J Virol       Date:  1989-03       Impact factor: 5.103

2.  Nucleotide sequences of the joint between the L and S segments of herpes simplex virus types 1 and 2.

Authors:  A J Davison; N M Wilkie
Journal:  J Gen Virol       Date:  1981-08       Impact factor: 3.891

3.  The segment inversion site of herpes simplex virus type 1 adopts a novel DNA structure.

Authors:  F Wohlrab; M J McLean; R D Wells
Journal:  J Biol Chem       Date:  1987-05-05       Impact factor: 5.157

Review 4.  The chemistry and biology of unusual DNA structures adopted by oligopurine.oligopyrimidine sequences.

Authors:  R D Wells; D A Collier; J C Hanvey; M Shimizu; F Wohlrab
Journal:  FASEB J       Date:  1988-11       Impact factor: 5.191

5.  Short, duplicated sequence indicative of the recombinogenicity of the junction between a unique and an inverted repeat sequence in the S component of the herpes simplex virus type 1 genome.

Authors:  K Umene
Journal:  J Virol       Date:  1989-05       Impact factor: 5.103

6.  Recombinogenic properties of herpes simplex virus type 1 DNA sequences resident in simian virus 40 minichromosomes.

Authors:  P C Weber; M Levine; J C Glorioso
Journal:  J Virol       Date:  1990-01       Impact factor: 5.103

7.  The cleavage recognition signal is contained within sequences surrounding an a-a junction in herpes simplex virus DNA.

Authors:  M Nasseri; E S Mocarski
Journal:  Virology       Date:  1988-11       Impact factor: 3.616

8.  Sequence requirements for DNA rearrangements induced by the terminal repeat of herpes simplex virus type 1 KOS DNA.

Authors:  J R Smiley; J Duncan; M Howes
Journal:  J Virol       Date:  1990-10       Impact factor: 5.103

9.  Reiterated sequences of herpes simplex virus type 1 (HSV-1) genome can serve as physical markers for the differentiation of HSV-1 strains.

Authors:  K Umene; M Yoshida
Journal:  Arch Virol       Date:  1989       Impact factor: 2.574

10.  The herpes simplex virus type 2 (HG52) variant JH2604 has a 1488 bp deletion which eliminates neurovirulence in mice.

Authors:  M Y Taha; G B Clements; S M Brown
Journal:  J Gen Virol       Date:  1989-11       Impact factor: 3.891

View more
  4 in total

1.  Sequences within the herpesvirus-conserved pac1 and pac2 motifs are required for cleavage and packaging of the murine cytomegalovirus genome.

Authors:  M A McVoy; D E Nixon; S P Adler; E S Mocarski
Journal:  J Virol       Date:  1998-01       Impact factor: 5.103

2.  Cleavage in and around the DR1 element of the A sequence of herpes simplex virus type 1 relevant to the excision of DNA fragments with length corresponding to one and two units of the A sequence.

Authors:  K Umene
Journal:  J Virol       Date:  2001-07       Impact factor: 5.103

3.  Inhibition of generation of authentic genomic termini of herpes simplex virus type 1 DNA in temperature-sensitive mutant BHK-21 cells with a mutated CCG1/TAF(II)250 gene.

Authors:  K Umene; T Nishimoto
Journal:  J Virol       Date:  1996-12       Impact factor: 5.103

4.  Dramatic effects of 2-bromo-5,6-dichloro-1-beta-D-ribofuranosyl benzimidazole riboside on the genome structure, packaging, and egress of guinea pig cytomegalovirus.

Authors:  Daniel E Nixon; Michael A McVoy
Journal:  J Virol       Date:  2004-02       Impact factor: 5.103

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.