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PMID: 2154589 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The herpes simplex virus 1 gene for ICP34.5, which maps in inverted repeats, is conserved in several limited-passage isolates but not in strain 17syn+.

Journal of virology ·Vol. 64 ·No. 3 ·1990-03-00 ·Pages 1014-20

Chou J, Roizman B

Abstract

In a previous study, it was reported that herpes simplex virus 1 (HSV-1) strain F contains a transcribed open reading frame situated in the inverted repeats of the L component between the terminal a sequence and the open reading frame that encodes the alpha 0 gene (J. Chou and B. Roizman, J. Virol. 57: 629-637, 1986). By means of an antibody to repeats of the trimer Ala-Thr-Pro predicted to be specified by the open reading frame, it was shown that the open reading frame specifies a protein (M. Ackermann, J. Chou, M. Sarmiento, R. A. Lerner, and B. Roizman, J. Virol. 58: 843-850, 1986). This open reading frame is absent from the reported sequence of HSV-1(17)syn+ (D. J. McGeoch, M. A. Dalrymple, A. J. Davison, A. Dolan, M. C. Frame, D. McNab, L. J. Perry, J. E. Scott, and P. Taylor, J. Gen. Virol. 69: 1531-1574, 1988; L. J. Perry and D. J. McGeoch, J. Gen. Virol. 69: 2831-2846, 1988). To define the extent of variability in this open reading frame, we compared the sequences of the ICP34.5-encoding open reading frames of the genomes of three strains characterized by limited passage in cell culture with that of the HSV-1(17)syn+ strain. Furthermore, to establish unambiguously that the antibody to the Ala-Thr-Pro repeats reacts with the product of this open reading frame, we inserted a short sequence that encodes a known epitope in frame at the 5' terminus of the coding domain. Our results indicate that with minor variations, the open reading frame is conserved in the three HSV-1 genomes analyzed but not in HSV-1(17)syn+. Thus, two strains contain an inserted amino acid and one strain, isolated from a case of human encephalitis, lacks a seven-amino-acid sequence. The recombinant virus carrying the foreign epitope expressed a slightly slower-migrating protein which reacted with both the rabbit polyclonal antibody to the Ala-Thr-Pro trimer repeats and the monoclonal antibody to the inserted epitope. The implications of the results are discussed.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Cloning, Molecular DNA, Viral/genetics Genes, Viral Humans Molecular Sequence Data Repetitive Sequences, Nucleic Acid Restriction Mapping Simplexvirus/genetics,isolation & purification Vero Cells
Chemicals
DNA, Viral
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Chou J
Marjorie B. Kovler Viral Oncology Laboratories, University of Chicago, Illinois 60637.
Roizman B
References (36)
36 references, click to expand
  1. Signals for site-specific cleavage of HSV DNA: maturation involves two separate cleavage events at sites distal to the recognition sequences.
    Cell. 1985 Jul;41(3):793-802 PMID: 2988788
  2. Evidence for a direct role for both the 175,000- and 110,000-molecular-weight immediate-early proteins of herpes simplex virus in the transactivation of delayed-early promoters.
    J Virol. 1985 Mar;53(3):751-60 PMID: 2983086
  3. Identification of immediate early genes from herpes simplex virus that transactivate the virus thymidine kinase gene.
    Proc Natl Acad Sci U S A. 1985 Aug;82(16):5265-9 PMID: 2991915
  4. Three trans-acting regulatory proteins of herpes simplex virus modulate immediate-early gene expression in a pathway involving positive and negative feedback regulation.
    J Virol. 1985 Dec;56(3):723-33 PMID: 2999428
  5. The terminal a sequence of the herpes simplex virus genome contains the promoter of a gene located in the repeat sequences of the L component.
    J Virol. 1986 Feb;57(2):629-37 PMID: 3003394
  6. Complete DNA sequence of the short repeat region in the genome of herpes simplex virus type 1.
    Nucleic Acids Res. 1986 Feb 25;14(4):1727-45 PMID: 3005980
  7. Identification by antibody to a synthetic peptide of a protein specified by a diploid gene located in the terminal repeats of the L component of herpes simplex virus genome.
    J Virol. 1986 Jun;58(3):843-50 PMID: 3009891
  8. Functional domains within the a sequence involved in the cleavage-packaging of herpes simplex virus DNA.
    J Virol. 1986 Sep;59(3):605-18 PMID: 3016323
  9. Characterization of the IE110 gene of herpes simplex virus type 1.
    J Gen Virol. 1986 Nov;67 ( Pt 11):2365-80 PMID: 3023529
  10. Co-ordinate regulation of herpes simplex virus gene expression is mediated by the functional interaction of two immediate early gene products.
    J Mol Biol. 1986 Oct 5;191(3):395-409 PMID: 3029383
  11. Genetic and biological analyses of a herpes simplex virus intertypic recombinant reduced specifically for neurovirulence.
    J Virol. 1987 Jun;61(6):1978-84 PMID: 3033324
  12. Herpes simplex virus immediate-early promoters are responsive to virus and cell trans-acting factors.
    J Virol. 1987 Jul;61(7):2286-96 PMID: 3035226
  13. A detailed mutational analysis of Vmw110, a trans-acting transcriptional activator encoded by herpes simplex virus type 1.
    EMBO J. 1987 Jul;6(7):2069-76 PMID: 2820720
  14. Mapping of functional and antigenic domains of the alpha 4 protein of herpes simplex virus 1.
    J Virol. 1988 Feb;62(2):454-62 PMID: 2447289
  15. The complete DNA sequence of the long unique region in the genome of herpes simplex virus type 1.
    J Gen Virol. 1988 Jul;69 ( Pt 7):1531-74 PMID: 2839594
  16. In vivo behavior of genetically engineered herpes simplex viruses R7017 and R7020: construction and evaluation in rodents.
    J Infect Dis. 1988 Sep;158(3):602-14 PMID: 2842408
  17. The DNA sequences of the long repeat region and adjoining parts of the long unique region in the genome of herpes simplex virus type 1.
    J Gen Virol. 1988 Nov;69 ( Pt 11):2831-46 PMID: 2846760
  18. The herpes simplex virus type 2 (HG52) variant JH2604 has a 1488 bp deletion which eliminates neurovirulence in mice.
    J Gen Virol. 1989 Nov;70 ( Pt 11):3073-8 PMID: 2555437
  19. Characterization of herpes simplex virus strains differing in their effects on social behaviour of infected cells.
    J Gen Virol. 1968 May;2(3):357-64 PMID: 4300104
  20. Size, composition, and structure of the deoxyribonucleic acid of herpes simplex virus subtypes 1 and 2.
    J Virol. 1971 Aug;8(2):125-32 PMID: 4329966
  21. Genetic studies with herpes simplex virus type 1. The isolation of temperature-sensitive mutants, their arrangement into complementation groups and recombination analysis leading to a linkage map.
    J Gen Virol. 1973 Mar;18(3):329-46 PMID: 4348796
  22. Proteins specified by herpes simplex virus. XI. Identification and relative molar rates of synthesis of structural and nonstructural herpes virus polypeptides in the infected cell.
    J Virol. 1973 Dec;12(6):1347-65 PMID: 4357511
  23. Anatomy of herpes simplex virus DNA. II. Size, composition, and arrangement of inverted terminal repetitions.
    J Virol. 1975 Jun;15(6):1487-97 PMID: 167196
  24. Inverted repetitions in the chromosome of herpes simplex virus.
    Cold Spring Harb Symp Quant Biol. 1975;39 Pt 2:667-78 PMID: 169022
  25. Anatomy of herpes simplex virus DNA: evidence for four populations of molecules that differ in the relative orientations of their long and short components.
    Proc Natl Acad Sci U S A. 1975 Nov;72(11):4243-7 PMID: 172900
  26. Transmission of herpes-simplex virus type 1 in a nursery for the newborn. Identification of viral isolates by D.N.A. "fingerprinting".
    Lancet. 1978 May 6;1(8071):964-6 PMID: 76893
  27. Anatomy of herpes simplex virus (HSV) DNA. X. Mapping of viral genes by analysis of polypeptides and functions specified by HSV-1 X HSV-2 recombinants.
    J Virol. 1978 May;26(2):389-410 PMID: 207894
  28. Temporal cluster of herpes simplex encephalitis: investigation by restriction endonuclease cleavage of viral DNA.
    J Infect Dis. 1980 Apr;141(4):436-40 PMID: 6246175
  29. A generalized technique for deletion of specific genes in large genomes: alpha gene 22 of herpes simplex virus 1 is not essential for growth.
    Cell. 1981 Jul;25(1):227-32 PMID: 6268303
  30. Site-specific inversion sequence of the herpes simplex virus genome: domain and structural features.
    Proc Natl Acad Sci U S A. 1981 Nov;78(11):7047-51 PMID: 6273905
  31. Ocular disease pattern induced by herpes simplex virus is genetically determined by a specific region of viral DNA.
    J Exp Med. 1982 Feb 1;155(2):475-89 PMID: 6276491
  32. The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers.
    Gene. 1982 Oct;19(3):259-68 PMID: 6295879
  33. Structure and role of the herpes simplex virus DNA termini in inversion, circularization and generation of virion DNA.
    Cell. 1982 Nov;31(1):89-97 PMID: 6297756
  34. Application of denatured, electrophoretically separated, and immobilized lysates of herpes simplex virus-infected cells for detection of monoclonal antibodies and for studies of the properties of viral proteins.
    J Virol. 1983 Apr;46(1):103-12 PMID: 6298448
  35. Trans activation of transcription by herpes virus products: requirement for two HSV-1 immediate-early polypeptides for maximum activity.
    EMBO J. 1984 Dec 20;3(13):3135-41 PMID: 6098466
  36. Isomerization of herpes simplex virus 1 genome: identification of the cis-acting and recombination sites within the domain of the a sequence.
    Cell. 1985 Jul;41(3):803-11 PMID: 2988789
Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1990-03-00
Pages
1014-20
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC249211
Subset
IM
Grants
NIAID NIH HHS · AI124009 · United States
NIAID NIH HHS · AI1588-11 · United States
NCI NIH HHS · CA47451 · United States
Databases
GENBANK
M33699, M33700, M33701
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