An Epstein-Barr virus nuclear protein 2 domain essential for transformation is a direct transcriptional activator
- PMID: 1656076
- PMCID: PMC250250
- DOI: 10.1128/JVI.65.11.5880-5885.1991
An Epstein-Barr virus nuclear protein 2 domain essential for transformation is a direct transcriptional activator
Abstract
Epstein-Barr virus nuclear protein 2 (EBNA-2) increases mRNA levels of specific viral and cellular genes through direct or indirect effects on upstream regulatory elements. The EBNA-2 domains essential for these effects have been partially defined and correlate with domains important for B-cell growth transformation. To determine whether EBNA-2 has a direct transcriptional activating domain, gene fusions between the DNA-binding domain of GAL4 and EBNA-2 were tested in CHO and B-lymphoma cells for the ability to activate transcription from target plasmids containing GAL4 recognition sites upstream of an adenovirus or murine mammary tumor virus promoter. In B-lymphoma cells, a 37-amino-acid EBNA-2 domain previously identified to be essential for transformation was nearly as strong a transcriptional activator as the activating domain of herpes simplex virus trans-inducing factor VP16. A quadradecapeptide had about 25% of the activating activity of the longer peptide. This first evidence that EBNA-2 directly activates transcription should facilitate the identification of nuclear factors with which EBNA-2 interacts in transactivation and transformation.
Similar articles
-
EBNA-2 of herpesvirus papio diverges significantly from the type A and type B EBNA-2 proteins of Epstein-Barr virus but retains an efficient transactivation domain with a conserved hydrophobic motif.J Virol. 1993 Jun;67(6):2990-3003. doi: 10.1128/JVI.67.6.2990-3003.1993. J Virol. 1993. PMID: 8388484 Free PMC article.
-
The EBNA-2 arginine-glycine domain is critical but not essential for B-lymphocyte growth transformation; the rest of region 3 lacks essential interactive domains.J Virol. 1994 Oct;68(10):6188-97. doi: 10.1128/JVI.68.10.6188-6197.1994. J Virol. 1994. PMID: 8083959 Free PMC article.
-
Identification of the Epstein-Barr virus nuclear antigen 2 transactivation domain.Biochem Biophys Res Commun. 1993 Feb 26;191(1):196-200. doi: 10.1006/bbrc.1993.1202. Biochem Biophys Res Commun. 1993. PMID: 8383488
-
Functional domains of Epstein-Barr virus nuclear antigen EBNA-1.J Virol. 1991 Mar;65(3):1466-78. doi: 10.1128/JVI.65.3.1466-1478.1991. J Virol. 1991. PMID: 1847464 Free PMC article.
-
Structure and function of the Epstein-Barr virus transcription factor, EBNA 3C.Curr Protein Pept Sci. 2006 Apr;7(2):123-36. doi: 10.2174/138920306776359777. Curr Protein Pept Sci. 2006. PMID: 16611138 Review.
Cited by
-
Protein kinase A associates with HA95 and affects transcriptional coactivation by Epstein-Barr virus nuclear proteins.Mol Cell Biol. 2002 Apr;22(7):2136-46. doi: 10.1128/MCB.22.7.2136-2146.2002. Mol Cell Biol. 2002. PMID: 11884601 Free PMC article.
-
Structural and functional characterization of a complex between the acidic transactivation domain of EBNA2 and the Tfb1/p62 subunit of TFIIH.PLoS Pathog. 2014 Mar 27;10(3):e1004042. doi: 10.1371/journal.ppat.1004042. eCollection 2014 Mar. PLoS Pathog. 2014. PMID: 24675874 Free PMC article.
-
A single amino acid in EBNA-2 determines superior B lymphoblastoid cell line growth maintenance by Epstein-Barr virus type 1 EBNA-2.J Virol. 2014 Aug;88(16):8743-53. doi: 10.1128/JVI.01000-14. Epub 2014 May 21. J Virol. 2014. PMID: 24850736 Free PMC article.
-
Contribution of conserved amino acids in mediating the interaction between EBNA2 and CBF1/RBPJk.J Virol. 1995 Mar;69(3):1944-50. doi: 10.1128/JVI.69.3.1944-1950.1995. J Virol. 1995. PMID: 7853539 Free PMC article.
-
PLK1-dependent phosphorylation restrains EBNA2 activity and lymphomagenesis in EBV-infected mice.EMBO Rep. 2021 Dec 6;22(12):e53007. doi: 10.15252/embr.202153007. Epub 2021 Oct 4. EMBO Rep. 2021. PMID: 34605140 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources