Identification of potential hot spots in the carboxy-terminal part of the Epstein-Barr virus (EBV), BNLF-1 gene in both malignant and benign EBV-associated diseases : high frequency of a 30-bp deletion in Malaysian and Danish peripheral T-cell lymphomas

In this study, we have sequenced the C-terminal part of the Epstein-Barr virus (EBV)-BNLF-1 gene encoding for the latent membrane protein-1 from tissues of EBV-positive Danish Hodgkin's disease (HD) and of Danish and Malaysian peripheral T-cell lymphomas (PTLs) and from tonsils of Danish infect...

Full description

Saved in:
Bibliographic Details
Published in:Blood Vol. 84; no. 12; pp. 4053 - 4060
Main Authors: SANDVEJ, K, SUAT-CHENG PEH, ANDRESEN, B. S, PALLESEN, G
Format: Journal Article
Language:English
Published: Washington, DC The Americain Society of Hematology 15-12-1994
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:In this study, we have sequenced the C-terminal part of the Epstein-Barr virus (EBV)-BNLF-1 gene encoding for the latent membrane protein-1 from tissues of EBV-positive Danish Hodgkin's disease (HD) and of Danish and Malaysian peripheral T-cell lymphomas (PTLs) and from tonsils of Danish infectious mononucleosis (IM). Our study showed that some of the 7 single-base mutations and the 30-bp deletion previously detected between codons of amino acid 322 and 366 in the BNLF-1 gene of the nasopharyngeal carcinoma cell line CAO were present in all Malaysian PTLs and in 60% of the Danish PTLs. In HD and the IM cases, the mutations were present in about 30%. The 30-bp deletion and the single base mutations occurred independently, and mutations were detectable in the majority of EBV type B-positive cases. These findings suggest that the 30-bp deletion and the 7 single-base mutations in the C-terminal part of the CAO-BNLF-1 gene do not characterize a new EBV type A substrain. Rather, some of the positions of single base mutations and the 30-bp deletion are hot spots that may have mutated independently through the evolution of EBV strains.
ISSN:0006-4971
1528-0020
DOI:10.1182/blood.V84.12.4053.bloodjournal84124053