INDUCTION OF AN EXCEPTIONALLY HIGH-LEVEL, NONTRANSLATED, EPSTEIN-BARRVIRUS-ENCODED POLYADENYLATED TRANSCRIPT IN THE BURKITTS-LYMPHOMA LINEDAUDI

Citation
Yn. Gao et al., INDUCTION OF AN EXCEPTIONALLY HIGH-LEVEL, NONTRANSLATED, EPSTEIN-BARRVIRUS-ENCODED POLYADENYLATED TRANSCRIPT IN THE BURKITTS-LYMPHOMA LINEDAUDI, Journal of virology, 71(1), 1997, pp. 84-94
Citations number
42
Categorie Soggetti
Virology
Journal title
ISSN journal
0022538X
Volume
71
Issue
1
Year of publication
1997
Pages
84 - 94
Database
ISI
SICI code
0022-538X(1997)71:1<84:IOAEHN>2.0.ZU;2-Q
Abstract
An Epstein-Barr virus transcript (designated D-HIT [Daudi high-level-i nducible transcript]), constitutively expressed at low levels in the B urkitt's lymphoma (BL)-derived cell line Daudi, can be induced with te tradecanoylphorbol acetate or n-butyrate or, in combination, to about 1% of the levels of high-molecular-weight RNAs in cells. The transcrip t can also be induced in some other EBV-positive BL-derived cells but to a much lesser extent, particularly in lines that can give rise to p roductive infection, D-HIT is viral in origin and is composed largely of repetitive sequence. It is polyadenylated hut mainly nuclear in loc ation and is highly structured, sensitive only to double-strand-specif ic RNase, It is endogenously expressed in interferon-sensitive Daudi s trains but not in an insensitive strain, Daudi 100K. D-HIT contains a part of a viral open reading frame (designated LF3, and deleted in the prototype B95-8 strain), using an internal polyadenylation (AAUAAA) s equence as a signal to specify processing of its 3' end, In Daudi cell s, the promoter contains a putative hinge structure, as found in some interferon-inducible genes and c-myc. Since D-HIT lies adjacent to, pr obably even encompassing, one of the two viral lytic origins (D-R) of replication, it may have a role in the regulation of DNA replication, Alternatively, or in addition via its double-stranded structure, D-HIT may play a regulatory role in interferon pathways. Its promoter could be of value for studying expression in constructions containing heter ologous genes.