Epstein-Barr virus induces cellular transcription factors to allow active expression of EBER genes by RNA polymerase III

被引:43
作者
Felton-Edkins, Zoe A.
Kondrashov, Alexander
Karali, Dimitra
Fairley, Jennifer A.
Dawson, Christopher W.
Arrand, John R.
Young, Lawrence S.
White, Robert J.
机构
[1] Univ Glasgow, Inst Biomed & Life Sci, Div Biochem & Mol Biol, Glasgow G12 8QQ, Lanark, Scotland
[2] Univ Birmingham, Sch Med, Canc Res UK, Inst Canc Studies, Birmingham B15 2TT, W Midlands, England
[3] Beatson Inst Canc Res, Glasgow G61 1BD, Lanark, Scotland
关键词
D O I
10.1074/jbc.M600468200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The EBER genes of Epstein-Barr virus (EBV) are transcribed by RNA polymerase (pol) III to produce untranslated RNAs that are implicated in oncogenesis. These EBER transcripts are the most highly expressed viral gene products in EBV-transformed cells. We have identified changes to the cellular transcription machinery that may contribute to the high levels of EBER RNA. These include phosphorylation of ATF2, which interacts with EBER promoters. A second is induction of TFIIIC, a pol III-specific factor that activates EBER genes; all five subunits of TFIIIC are overexpressed in EBV-positive cells. In addition, EBV induces BDP1, a subunit of the pol III-specific factor TFIIIB. Although BDP1 is the only TFIIIB subunit induced by EBV, its induction is sufficient to stimulate EBER expression in vivo, implying a limiting function. The elevated levels of BDP1 and TFIIIC in EBV-positive cells stimulate production of tRNA, 7SL, and 5S rRNA. Abnormally high expression of these cellular pol III products may contribute to the ability of EBV to enhance growth potential.
引用
收藏
页码:33871 / 33880
页数:10
相关论文
共 60 条
[1]   Epstein-Barr virus immediate-early proteins BZLF1 and BRLF1 activate the ATF2 transcription factor by increasing the levels of phosphorylated p38 and c-Jun N-terminal kinases [J].
Adamson, AL ;
Darr, D ;
Holley-Guthrie, E ;
Johnson, RA ;
Mauser, A ;
Swenson, J ;
Kenney, S .
JOURNAL OF VIROLOGY, 2000, 74 (03) :1224-1233
[2]   CHARACTERIZATION OF THE MAJOR EPSTEIN-BARR VIRUS-SPECIFIC RNA IN BURKITT LYMPHOMA-DERIVED CELLS [J].
ARRAND, JR ;
RYMO, L .
JOURNAL OF VIROLOGY, 1982, 41 (02) :376-389
[3]   2 FAMILIES OF SEQUENCES IN THE SMALL RNA-ENCODING REGION OF EPSTEIN-BARR VIRUS (EBV) CORRELATE WITH EBV TYPE-A AND TYPE-B [J].
ARRAND, JR ;
YOUNG, LS ;
TUGWOOD, JD .
JOURNAL OF VIROLOGY, 1989, 63 (02) :983-986
[4]  
ARRAND JR, 2000, EBV REP, V7, P145
[5]   p53 is a general repressor of RNA polymerase III transcription [J].
Cairns, CA ;
White, RJ .
EMBO JOURNAL, 1998, 17 (11) :3112-3123
[6]   Deregulation of RNA polymerase III transcription in cervical epithelium in response to high-risk human papillomavirus [J].
Daly, NL ;
Arvanitis, DA ;
Fairley, JA ;
Gomez-Roman, N ;
Morton, JP ;
Graham, SV ;
Spandidos, DA ;
White, RJ .
ONCOGENE, 2005, 24 (05) :880-888
[7]   AP-1: A double-edged sword in tumorigenesis [J].
Eferl, R ;
Wagner, EF .
NATURE REVIEWS CANCER, 2003, 3 (11) :859-868
[8]   Activation of the cJun N-terminal kinase (JNK) pathway by the Epstein-Barr virus-encoded latent membrane protein 1 (LMP1) [J].
Eliopoulos, AG ;
Young, LS .
ONCOGENE, 1998, 16 (13) :1731-1742
[9]   The mitogen-activated protein (MAP) kinase ERK induces tRNA synthesis by phosphorylating TFIIIB [J].
Felton-Edkins, ZA ;
Fairley, JA ;
Graham, EL ;
Johnston, IM ;
White, RJ ;
Scott, PH .
EMBO JOURNAL, 2003, 22 (10) :2422-2432
[10]   Multiple mechanisms contribute to the activation of RNA polymerase III transcription in cells transformed by papovaviruses [J].
Felton-Edkins, ZA ;
White, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (50) :48182-48191