J Gen Virol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 74 (1993), 1393-1398; DOI 10.1099/0022-1317-74-7-1393
© 1993 Society for General Microbiology

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Trivedi, P.
Right arrow Articles by Masucci, M. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Trivedi, P.
Right arrow Articles by Masucci, M. G.
Agricola
Right arrow Articles by Trivedi, P.
Right arrow Articles by Masucci, M. G.

Integration of a short Epstein—Barr virus DNA fragment in a B95-8 virus converted Burkitt lymphoma line expressing Epstein—Barr nuclear antigens EBNA2 and EBNA5

Pankaj Trivedi, Laura Cuomo, Pedro Otavio de Campos-Lima, Marta P. Imreh, Karin Kvarnung, George Klein and Maria G. Masucci

Department of Tumour Biology, Karolinska Institute, Box 60400, S-104 01 Stockholm, Sweden

We have analysed the expression of transformation-associated viral antigens, the Epstein—Barr virus (EBV) DNA content and the phenotypic characteristics of two B95-8 virus-converted sublines of the EBV-negative Burkitt's lymphoma (BL) line BL28. The converted lines called E95A-BL28 and E95B-BL28, respectively, differed in their EBV gene expression. The E95B convertant expressed virus-encoded nuclear antigens EBNA1 to -6 and the membrane protein LMP1, but only EBNA2 and EBNA5 were detected by immunofluorescence and immunoblotting in the E95A convertant. Only the entire BamHI W, Y and H regions could be detected in the E95A convertant by hybridization of Southern blots with probes covering the BamHI C, W, Y, H, F, E, K and Nhet regions of the EBV genome. EBV episomes were found to be absent in the E95A convertant as seen by Gardella gels. The E95A convertant retained the phenotypic characteristics of the EBV-negative parental line, and remained highly clonable in agarose. In contrast, expression of EBNA1 to -6 and LMP1 was accompanied by a shift towards a more lymphoblastoid cell line-like phenotype and by loss of agarose clonability in the E95B convertant.

Received 15 September 1992; accepted 2 February 1993.


This article has been cited by other articles:


Home page
Am. J. Pathol.Home page
A. Staratschek-Jox, S. Kotkowski, G. Belge, T. Rudiger, J. Bullerdiek, V. Diehl, and J. Wolf
Detection of Epstein-Barr Virus in Hodgkin-Reed-Sternberg Cells : No Evidence for the Persistence of Integrated Viral Fragments inLatent Membrane Protein-1 (LMP-1)-Negative Classical Hodgkin’s Disease
Am. J. Pathol., January 1, 2000; 156(1): 209 - 216.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
L. Holmgren, A. Szeles, E. Rajnavolgyi, J. Folkman, G. Klein, I. Ernberg, and K. I. Falk
Horizontal Transfer of DNA by the Uptake of Apoptotic Bodies
Blood, June 1, 1999; 93(11): 3956 - 3963.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1993 by the Society for General Microbiology.