EFFICIENT EBV SUPERINFECTION OF GROUP-I BURKITTS-LYMPHOMA CELLS DISTINGUISHES REQUIREMENTS FOR EXPRESSION OF THE CP VIRAL PROMOTER AND CAN ACTIVATE THE EBV PRODUCTIVE CYCLE

被引:15
作者
EVANS, TJ [1 ]
JACQUEMIN, MG [1 ]
FARRELL, PJ [1 ]
机构
[1] ST MARYS HOSP,SCH MED,LUDWIG INST CANC RES,LONDON W2 1PG,ENGLAND
关键词
D O I
10.1006/viro.1995.1009
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Group I Burkitt's lymphoma cell lines conditionally expressing the CD21 receptor for EBV infection were superinfected with EBV. The incoming EBV entered its normal program of gene expression, producing EBNA-2 and LMP-1 and activating the Cp EBNA promoter, but the endogenous virus in the BL lines was not induced to express EBNA-2 or transcribe RNA from Cp. LMP-1 was, however, expressed from the endogenous genome in response to superinfection. in a proportion of the superinfected Akata cells, the productive cycle antigen BZLF1 was induced and the ability of infecting virus to cause this was sensitive to inactivation by uv light. The results show that the restricted latent pattern of EBV gene expression observed in Group I BL cells is not a consequence of lack of appropriate transcription factor activity but results from inactivation of part of the viral genome, probably by methylation. Induction of BZLF1 in some of the cells also indicates a novel pathway for activation of the virus productive cycle. (C) 1995 Academic Press, Inc.
引用
收藏
页码:866 / 877
页数:12
相关论文
共 50 条
[11]   AUTOREGULATION OF EPSTEIN-BARR VIRUS PUTATIVE LYTIC SWITCH GENE BZLF1 [J].
FLEMINGTON, E ;
SPECK, SH .
JOURNAL OF VIROLOGY, 1990, 64 (03) :1227-1232
[12]   DIFFERENT EPSTEIN-BARR VIRUS-B CELL-INTERACTIONS IN PHENOTYPICALLY DISTINCT CLONES OF A BURKITTS-LYMPHOMA CELL-LINE [J].
GREGORY, CD ;
ROWE, M ;
RICKINSON, AB .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :1481-1495
[13]   THE EPSTEIN-BARR-VIRUS NUCLEAR ANTIGEN-2 TRANSACTIVATOR IS DIRECTED TO RESPONSE ELEMENTS BY THE J-KAPPA RECOMBINATION SIGNAL BINDING-PROTEIN [J].
GROSSMAN, SR ;
JOHANNSEN, E ;
TONG, X ;
YALAMANCHILI, R ;
KIEFF, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (16) :7568-7572
[14]   BIOCHEMICAL AND IMMUNOLOGICAL CHARACTERIZATION OF THE DNA-BINDING PROTEIN (RBP-J-KAPPA) TO MOUSE J-KAPPA RECOMBINATION SIGNAL SEQUENCE [J].
HAMAGUCHI, Y ;
YAMAMOTO, Y ;
IWANARI, H ;
MARUYAMA, S ;
FURUKAWA, T ;
MATSUNAMI, N ;
HONJO, T .
JOURNAL OF BIOCHEMISTRY, 1992, 112 (03) :314-320
[15]   MEDIATION OF EPSTEIN-BARR-VIRUS EBNA2 TRANSACTIVATION BY RECOMBINATION SIGNAL-BINDING PROTEIN J(K) [J].
HENKEL, T ;
LING, PD ;
HAYWARD, SD ;
PETERSON, MG .
SCIENCE, 1994, 265 (5168) :92-95
[16]  
JACQUEMIN MG, 1993, INSERUM C, V225, P43
[17]   IDENTIFICATION OF CRITICAL CIS ELEMENTS INVOLVED IN MEDIATING EPSTEIN-BARR-VIRUS NUCLEAR ANTIGEN 2-DEPENDENT ACTIVITY OF AN ENHANCER LOCATED UPSTREAM OF THE VIRAL BAMHI C-PROMOTER [J].
JIN, XW ;
SPECK, SH .
JOURNAL OF VIROLOGY, 1992, 66 (05) :2846-2852
[18]  
KLEIN G, 1975, INTERVIROLOGY, V5, P319, DOI 10.1159/000149930
[19]   IDENTIFICATION OF A GLUCOCORTICOID-RESPONSIVE ELEMENT IN EPSTEIN-BARR-VIRUS [J].
KUPFER, SR ;
SUMMERS, WC .
JOURNAL OF VIROLOGY, 1990, 64 (05) :1984-1990
[20]   DIFFERENTIAL SPLICING OF EPSTEIN-BARR-VIRUS IMMEDIATE-EARLY RNA [J].
LAU, R ;
PACKHAM, G ;
FARRELL, PJ .
JOURNAL OF VIROLOGY, 1992, 66 (10) :6233-6236