» Articles » PMID: 1847471

Variable Expression of Latent Membrane Protein in Nasopharyngeal Carcinoma Can Be Related to Methylation Status of the Epstein-Barr Virus BNLF-1 5'-flanking Region

Overview
Journal J Virol
Date 1991 Mar 1
PMID 1847471
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

Seven virus-coded proteins, the nuclear proteins EBNA-1 to EBNA-6 and the latent membrane protein (LMP), are regularly expressed in Epstein-Barr virus (EBV)-transformed lymphoblastoid cell lines. In nasopharyngeal carcinoma (NPC), only EBNA-1 is regularly expressed; LMP is detected in about 65% of the tumors. In Burkitt's lymphoma tumors only EBNA-1 is expressed. We have recently shown that the methylation patterns of the EBV genome varied between these cell types. In virally transformed lymphoblastoid cell lines of normal origin, the EBV DNA is completely unmethylated. In contrast, in the Burkitt's lymphoma-derived cell line Rael and in a nude mouse-passaged NPC tumor, C15, there was an extensive methylation of CpG pairs. The methylation extended into the coding regions of the two expressed genes, EBNA-1 (in both tumor types) and LMP (in C15). Two presumptive control regions were exempted from this overall methylation: the oriP that contains both an origin of DNA replication and an EBNA-1-dependent enhancer and the 5'-flanking region of the BNLF-1 open reading frame that codes for LMP. The latter was only exempted in the LMP expressing NPC. We have now investigated the relation between expression of LMP and methylation of DNA in the 5'-flanking 1 kb region of BNLF-1, coding for LMP. LMP was methylated in 3 of 12 NPC biopsies that did not express LMP but was partially or totally unmethylated in the remaining 9 that expressed the protein. The three BNLF-1 exons were highly methylated in all the tumors. The oriP region was unmethylated in all the tumors, as in the previously studied Rael cell line and nude mouse-passaged NPC. Also, the BamHI W enhancer region involved in the expression of EBNA nuclear proteins was methylated. None of the biopsies expressed EBNA-2. Our data show that the EBV genomes are highly methylated in NPC tumors. The strong reverse correlation between the methylation of the putative control region of the LMP gene and the expression of LMP suggests that methylation has a role in the regulation of this gene.

Citing Articles

Targeting the crosstalk of epigenetic modifications and immune evasion in nasopharyngeal cancer.

Looi C, Foong L, Chung F, Khoo A, Loo E, Leong C Cell Biol Toxicol. 2023; 39(6):2501-2526.

PMID: 37755585 DOI: 10.1007/s10565-023-09830-9.


MC180295 Inhibited Epstein-Barr Virus-Associated Gastric Carcinoma Cell Growth by Suppressing DNA Repair and the Cell Cycle.

Fujii T, Nishikawa J, Fukuda S, Kubota N, Nojima J, Fujisawa K Int J Mol Sci. 2022; 23(18).

PMID: 36142506 PMC: 9500863. DOI: 10.3390/ijms231810597.


The Role of Epigenetic Regulation in Epstein-Barr Virus-Associated Gastric Cancer.

Nishikawa J, Iizasa H, Yoshiyama H, Nakamura M, Saito M, Sasaki S Int J Mol Sci. 2017; 18(8).

PMID: 28757548 PMC: 5577998. DOI: 10.3390/ijms18081606.


The Epstein-Barr virus encoded LMP1 oncoprotein modulates cell adhesion via regulation of activin A/TGFβ and β1 integrin signalling.

Morris M, Dawson C, Laverick L, Davis A, Dudman J, Raveenthiraraj S Sci Rep. 2016; 6:19533.

PMID: 26782058 PMC: 4726061. DOI: 10.1038/srep19533.


Detection of nasopharyngeal carcinoma in Morocco (North Africa) using a multiplex methylation-specific PCR biomarker assay.

Nawaz I, Moumad K, Martorelli D, Ennaji M, Zhou X, Zhang Z Clin Epigenetics. 2015; 7:89.

PMID: 26300994 PMC: 4546349. DOI: 10.1186/s13148-015-0119-8.


References
1.
Becker P, Ruppert S, Schutz G . Genomic footprinting reveals cell type-specific DNA binding of ubiquitous factors. Cell. 1987; 51(3):435-43. DOI: 10.1016/0092-8674(87)90639-8. View

2.
Kovesdi I, Reichel R, Nevins J . Role of an adenovirus E2 promoter binding factor in E1A-mediated coordinate gene control. Proc Natl Acad Sci U S A. 1987; 84(8):2180-4. PMC: 304612. DOI: 10.1073/pnas.84.8.2180. View

3.
Watt F, Molloy P . Cytosine methylation prevents binding to DNA of a HeLa cell transcription factor required for optimal expression of the adenovirus major late promoter. Genes Dev. 1988; 2(9):1136-43. DOI: 10.1101/gad.2.9.1136. View

4.
Hennessy K, Fennewald S, Hummel M, Cole T, Kieff E . A membrane protein encoded by Epstein-Barr virus in latent growth-transforming infection. Proc Natl Acad Sci U S A. 1984; 81(22):7207-11. PMC: 392107. DOI: 10.1073/pnas.81.22.7207. View

5.
Kelley D, Pollok B, Atchison M, PERRY R . The coupling between enhancer activity and hypomethylation of kappa immunoglobulin genes is developmentally regulated. Mol Cell Biol. 1988; 8(2):930-7. PMC: 363225. DOI: 10.1128/mcb.8.2.930-937.1988. View