Literature DB >> 6273905

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

E S Mocarski, B Roizman.   

Abstract

The genome of herpes simplex virus-1 consists of two covalently linked components, L and S, that invert relative to each other. The L and S components consist of unique DNA sequences bracketed by inverted repeats. The inverted repeats of the L component are designated ab and b' a' and those of the S component are designated a' c' and ca. The number of a sequences at the termini and at the L-S component junction varies from one to several copies. Insertion into the middle of the L component of a DNA fragment consisting of 156 base pairs (bp) of the b sequence, an entire a sequence of 501 bp, and 618 bp of the c sequence created a new site through which additional inversions in the genome occurred. Comparison of the nucleotide sequences of DNA fragments containing one and two a sequences defined the domain of the a sequence. The single a sequence consists of two 20-bp direct repeats (designated as DR1) bracketing a region that contains 19 tandem direct repeats of a 12-bp sequence (DR2) adjacent to three direct repeats of a 37-bp sequence (DR4), in addition to short stretches of unique sequences. The fragment with two tandem a sequences contained three copies of DR1-i.e., the intervening DR1 was shared by the two a sequences. Furthermore, one a sequence contained 22 copies of DR2 and two copies of DR4 whereas the second a sequence contained 19 copies of DR2 and two copies of DR4. These observations suggest that (i) amplification of the number of terminal and internal a sequences is the consequence of intramolecular or intermolecular recombination through DR1, (ii) the number of copies of DR2 and DR4 within the a sequence is not fixed and may vary as a consequence of unequal crossing over or slippage, and (iii) inversion results from intramolecular recombination between terminal and inverted a sequences.

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Year:  1981        PMID: 6273905      PMCID: PMC349191          DOI: 10.1073/pnas.78.11.7047

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  16 in total

1.  Polynucleotide kinase exchange reaction: quantitave assay for restriction endonuclease-generated 5'-phosphoroyl termini in DNA.

Authors:  K L Berkner; W R Folk
Journal:  J Biol Chem       Date:  1977-05-25       Impact factor: 5.157

2.  Anatomy of herpes simplex virus DNA. XII. Accumulation of head-to-tail concatemers in nuclei of infected cells and their role in the generation of the four isomeric arrangements of viral DNA.

Authors:  R J Jacob; L S Morse; B Roizman
Journal:  J Virol       Date:  1979-02       Impact factor: 5.103

3.  Structure of the joint region and the termini of the DNA of herpes simplex virus type 1.

Authors:  M J Wagner; W C Summers
Journal:  J Virol       Date:  1978-08       Impact factor: 5.103

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

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

5.  Anatomy of herpes simplex virus DNA. V. Terminally repetitive sequences.

Authors:  S Wadsworth; G S Hayward; B Roizman
Journal:  J Virol       Date:  1976-02       Impact factor: 5.103

6.  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

7.  Transformation in Escherichia coli: cryogenic preservation of competent cells.

Authors:  D A Morrison
Journal:  J Bacteriol       Date:  1977-10       Impact factor: 3.490

8.  Cloning of reiterated and nonreiterated herpes simplex virus 1 sequences as BamHI fragments.

Authors:  L E Post; A J Conley; E S Mocarski; B Roizman
Journal:  Proc Natl Acad Sci U S A       Date:  1980-07       Impact factor: 11.205

9.  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

10.  Size, composition, and structure of the deoxyribonucleic acid of herpes simplex virus subtypes 1 and 2.

Authors:  E D Kieff; S L Bachenheimer; B Roizman
Journal:  J Virol       Date:  1971-08       Impact factor: 5.103

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  83 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.  Isomerization of a uniquely designed amplicon during herpes simplex virus-mediated replication.

Authors:  H Wang; X Fu; X Zhang
Journal:  J Virol       Date:  2001-11       Impact factor: 5.103

3.  Intracellular Cre-mediated deletion of the unique packaging signal carried by a herpes simplex virus type 1 recombinant and its relationship to the cleavage-packaging process.

Authors:  C Logvinoff; A L Epstein
Journal:  J Virol       Date:  2000-09       Impact factor: 5.103

4.  Characterization of a herpes simplex virus sequence which binds a cellular protein as either a single-stranded or double-stranded DNA or RNA.

Authors:  L McCormick; R J Roller; B Roizman
Journal:  J Virol       Date:  1992-06       Impact factor: 5.103

5.  A cluster of dispensable genes within the human cytomegalovirus genome short component: IRS1, US1 through US5, and the US6 family.

Authors:  T R Jones; V P Muzithras
Journal:  J Virol       Date:  1992-04       Impact factor: 5.103

6.  A host cell protein binds to a highly conserved sequence element (pac-2) within the cytomegalovirus a sequence.

Authors:  G W Kemble; E S Mocarski
Journal:  J Virol       Date:  1989-11       Impact factor: 5.103

7.  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

8.  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

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

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