Home LiteratureArticle Details
PMID: 2536113 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Two related Epstein-Barr virus membrane proteins are encoded by separate genes.

Journal of virology ·Vol. 63 ·No. 2 ·1989-02-00 ·Pages 933-7

Sample J, Liebowitz D, Kieff E

Abstract

The structures of the 2.3- and 2.0-kilobase Epstein-Barr virus (EBV) mRNAs, partially encoded within the EcoRI J fragment DNA of the viral genome, were determined by analysis of their cDNAs. Both mRNAs are transcribed across the fused terminal repeats of the EBV episome and consist of nine exons. The mRNAs are transcribed from different promoters and have a unique 5' exon from the U5 region of the genome but eight common exons from the U1 region. One principal open reading frame is present in each mRNA and is predicted to encode 54,000- and 40,000-dalton integral membrane proteins. This result was confirmed by in vitro translation of RNAs in the presence of canine pancreatic microsomes. The 2.3-kilobase mRNA is not expressed in Raji cells, owing to the deletion of the 5' regulatory and coding region of this gene, whereas neither mRNA is expressed in Namalwa cells, owing to inactivation as a result of integration of the EBV genome via the terminal repeats. Since these mRNAs are readily detected in largely latently infected cells and do not increase in abundance with EBV replication, these putative latent-infection membrane proteins are tentatively designated LMP-2A and LMP-2B, respectively.

MeSH Terms
Amino Acid Sequence Antigens, Viral/genetics Base Sequence DNA/genetics Exons Genes Genes, Viral Herpesvirus 4, Human/genetics Molecular Sequence Data RNA, Messenger/genetics RNA, Viral/genetics Viral Matrix Proteins
Chemicals
Antigens, Viral EBV-associated membrane antigen, Epstein-Barr virus RNA, Messenger RNA, Viral Viral Matrix Proteins DNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Sample J
Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115.
Liebowitz D
Kieff E
References (34)
34 references, click to expand
  1. Epstein-Barr virus nuclear antigen 2 specifically induces expression of the B-cell activation antigen CD23.
    Proc Natl Acad Sci U S A. 1987 May;84(10):3452-6 PMID: 3033649
  2. 3' non-coding region sequences in eukaryotic messenger RNA.
    Nature. 1976 Sep 16;263(5574):211-4 PMID: 822353
  3. Sensitive, high-resolution chromatin and chromosome mapping in situ: presence and orientation of two closely integrated copies of EBV in a lymphoma line.
    Cell. 1988 Jan 15;52(1):51-61 PMID: 2830981
  4. A fifth Epstein-Barr virus nuclear protein (EBNA3C) is expressed in latently infected growth-transformed lymphocytes.
    J Virol. 1988 Apr;62(4):1330-8 PMID: 2831394
  5. A sixth Epstein-Barr virus nuclear protein (EBNA3B) is expressed in latently infected growth-transformed lymphocytes.
    J Virol. 1988 Jun;62(6):2173-8 PMID: 2835517
  6. Epstein-Barr virus latent infection membrane protein alters the human B-lymphocyte phenotype: deletion of the amino terminus abolishes activity.
    J Virol. 1988 Nov;62(11):4173-84 PMID: 2845129
  7. Epstein-Barr virus (B95-8) DNA VII: molecular cloning and detailed mapping.
    Proc Natl Acad Sci U S A. 1980 May;77(5):2999-3003 PMID: 6248879
  8. Promoter sequences of eukaryotic protein-coding genes.
    Science. 1980 Sep 19;209(4463):1406-14 PMID: 6251548
  9. Epstein-Barr virus RNA VII: size and direction of transcription of virus-specified cytoplasmic RNAs in a transformed cell line.
    Proc Natl Acad Sci U S A. 1981 Mar;78(3):1930-4 PMID: 6112750
  10. Prediction of protein antigenic determinants from amino acid sequences.
    Proc Natl Acad Sci U S A. 1981 Jun;78(6):3824-8 PMID: 6167991
  11. Co-translational membrane integration of calcium pump protein without signal sequence cleavage.
    Nature. 1981 Jul 2;292(5818):87-8 PMID: 6456415
  12. A catalogue of splice junction sequences.
    Nucleic Acids Res. 1982 Jan 22;10(2):459-72 PMID: 7063411
  13. Epstein-Barr virus RNA. VIII. Viral RNA in permissively infected B95-8 cells.
    J Virol. 1982 Jul;43(1):262-72 PMID: 6180174
  14. Two deletions in the Epstein-Barr virus genome of the Burkitt lymphoma nonproducer line Raji.
    Virology. 1984 Feb;133(1):146-57 PMID: 6322426
  15. Nucleotide sequence of an mRNA transcribed in latent growth-transforming virus infection indicates that it may encode a membrane protein.
    J Virol. 1984 Aug;51(2):411-9 PMID: 6086953
  16. DNA sequence and expression of the B95-8 Epstein-Barr virus genome.
    Nature. 1984 Jul 19-25;310(5974):207-11 PMID: 6087149
  17. A membrane protein encoded by Epstein-Barr virus in latent growth-transforming infection.
    Proc Natl Acad Sci U S A. 1984 Nov;81(22):7207-11 PMID: 6095274
  18. Persistence of the entire Epstein-Barr virus genome integrated into human lymphocyte DNA.
    Science. 1984 Dec 14;226(4680):1322-5 PMID: 6095452
  19. Stable replication of plasmids derived from Epstein-Barr virus in various mammalian cells.
    Nature. 1985 Feb 28-Mar 6;313(6005):812-5 PMID: 2983224
  20. The detection and classification of membrane-spanning proteins.
    Biochim Biophys Acta. 1985 May 28;815(3):468-76 PMID: 3838905
  21. General method for the rapid solid-phase synthesis of large numbers of peptides: specificity of antigen-antibody interaction at the level of individual amino acids.
    Proc Natl Acad Sci U S A. 1985 Aug;82(15):5131-5 PMID: 2410914
  22. Translocation of secretory proteins across the microsomal membrane occurs through an environment accessible to aqueous perturbants.
    Cell. 1985 Sep;42(2):497-505 PMID: 2992801
  23. The short unique region of the B95-8 Epstein-Barr virus genome.
    Virology. 1985 Nov;147(1):81-98 PMID: 2998073
  24. An EBV membrane protein expressed in immortalized lymphocytes transforms established rodent cells.
    Cell. 1985 Dec;43(3 Pt 2):831-40 PMID: 3000618
  25. Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes.
    Cell. 1986 Jan 31;44(2):283-92 PMID: 3943125
  26. Nucleotide sequences of mRNAs encoding Epstein-Barr virus nuclear proteins: a probable transcriptional initiation site.
    Proc Natl Acad Sci U S A. 1986 Jul;83(14):5096-100 PMID: 3460083
  27. Simplified procedure for carrying out simultaneous multiple hydrogen fluoride cleavages of protected peptide resins.
    Int J Pept Protein Res. 1986 Jun;27(6):673-8 PMID: 3759338
  28. trans activation of an Epstein-Barr viral transcriptional enhancer by the Epstein-Barr viral nuclear antigen 1.
    Mol Cell Biol. 1986 Nov;6(11):3838-46 PMID: 3025615
  29. A bicistronic Epstein-Barr virus mRNA encodes two nuclear proteins in latently infected, growth-transformed lymphocytes.
    J Virol. 1987 Apr;61(4):945-54 PMID: 3029429
  30. A spliced Epstein-Barr virus gene expressed in immortalized lymphocytes is created by circularization of the linear viral genome.
    EMBO J. 1988 Mar;7(3):769-74 PMID: 2840285
  31. Sequence analysis of Raji Epstein-Barr virus DNA.
    Virology. 1988 Jun;164(2):334-40 PMID: 2835854
  32. Separation of Epstein-Barr virus DNA from large chromosomal DNA in non-virus-producing cells.
    Nat New Biol. 1972 Aug 9;238(84):169-71 PMID: 4340572
  33. Covalently closed circular duplex DNA of Epstein-Barr virus in a human lymphoid cell line.
    J Mol Biol. 1976 Apr 15;102(3):511-30 PMID: 178878
  34. An Epstein-Barr virus transforming protein associates with vimentin in lymphocytes.
    Mol Cell Biol. 1987 Jul;7(7):2299-308 PMID: 3039344
Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1989-02-00
Pages
933-7
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC247768
Subset
IM
Grants
NCI NIH HHS · CA-07967 · United States
NCI NIH HHS · CA-47006 · United States
NIGMS NIH HHS · GM-07281 · United States
Databases
GENBANK
M24212
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]