Literature DB >> 6270266

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

A J Davison, N M Wilkie.   

Abstract

The a sequence of herpes simplex virus (HSV) is present as a direct repeat at the genomic termini and also in inverted orientation at the joint between the L and S segments. DNA sequences have been determined for the joint regions of the genomes of HSV-1 and HSV-2, and relative to these sequences the genomic termini are in both cases located close to a short direct repeat of 17 to 21 base pairs (bp) at the b-a and a-c junctions. The HSV-1 joint region contains three separate tandem direct reiterations of short sequences, (12, 16 and 17 bp in strain 17) and we conclude that size heterogeneity in the a and c sequences is due to variable copy numbers of these repeated units. It is likely that a considerable part of the HSV-1 joint region does not code for polypeptide.

Entities:  

Mesh:

Substances:

Year:  1981        PMID: 6270266     DOI: 10.1099/0022-1317-55-2-315

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


  95 in total

1.  Machinery to support genome segment inversion exists in a herpesvirus which does not naturally contain invertible elements.

Authors:  M A McVoy; D Ramnarain
Journal:  J Virol       Date:  2000-05       Impact factor: 5.103

2.  Effects of mutations within the herpes simplex virus type 1 DNA encapsidation signal on packaging efficiency.

Authors:  P D Hodge; N D Stow
Journal:  J Virol       Date:  2001-10       Impact factor: 5.103

3.  Herpes simplex virus immediate-early protein ICP0 is targeted by SIAH-1 for proteasomal degradation.

Authors:  Claus-Henning Nagel; Nina Albrecht; Kristijana Milovic-Holm; Lakshmikanth Mariyanna; Britta Keyser; Bettina Abel; Britta Weseloh; Thomas G Hofmann; Martha M Eibl; Joachim Hauber
Journal:  J Virol       Date:  2011-06-01       Impact factor: 5.103

4.  Recombination of the internal direct repeat element DR2 responsible for the fluidity of the a sequence of herpes simplex virus type 1.

Authors:  K Umene
Journal:  J Virol       Date:  1991-10       Impact factor: 5.103

5.  Two open reading frames (ORF1 and ORF2) within the 2.0-kilobase latency-associated transcript of herpes simplex virus type 1 are not essential for reactivation from latency.

Authors:  M U Fareed; J G Spivack
Journal:  J Virol       Date:  1994-12       Impact factor: 5.103

6.  Herpes simplex virus type 1 recombination: the Uc-DR1 region is required for high-level a-sequence-mediated recombination.

Authors:  R E Dutch; B V Zemelman; I R Lehman
Journal:  J Virol       Date:  1994-06       Impact factor: 5.103

7.  Herpes simplex virus type 1 DNA replication is specifically required for high-frequency homologous recombination between repeated sequences.

Authors:  R E Dutch; V Bianchi; I R Lehman
Journal:  J Virol       Date:  1995-05       Impact factor: 5.103

8.  Replication origins and a sequence involved in coordinate induction of the immediate-early gene family are conserved in an intergenic region of herpes simplex virus.

Authors:  J L Whitton; J B Clements
Journal:  Nucleic Acids Res       Date:  1984-02-24       Impact factor: 16.971

9.  Herpes simplex virus type 1 restriction fragment polymorphism determined using southern hybridization.

Authors:  K Umene; T Eto; R Mori; Y Takagi; L W Enquist
Journal:  Arch Virol       Date:  1984       Impact factor: 2.574

10.  Fragments from both termini of the herpes simplex virus type 1 genome contain signals required for the encapsidation of viral DNA.

Authors:  N D Stow; E C McMonagle; A J Davison
Journal:  Nucleic Acids Res       Date:  1983-12-10       Impact factor: 16.971

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.