Epstein-Barr virus leader protein enhances EBNA-2-mediated transactivation of latent membrane protein 1 expression: a role for the W1W2 repeat domain

Epstein-Barr virus leader protein enhances EBNA-2-mediated transactivation of latent membrane protein 1 expression: a role for the W1W2 repeat domain
复制标题

Epstein-Barr 病毒前导蛋白增强 EBNA-2 介导的潜伏膜蛋白 1 表达的反式激活:W1W2 重复结构域的作用

DOI:
10.1128/jvi.71.9.6619-6628.1997
复制
发表时间:
1997
影响因子:
5.4
通讯作者:
A. Rickinson
A. Rickinson
中科院分区:
医学2区
文献类型:
--
作者:
Fiona Nitsche;A. Bell;A. Rickinson

文献摘要

参考文献

被引文献

相似文献

The Epstein-Barr virus (EBV)-encoded leader protein EBNA-LP is made up of several 66-amino-acid repeats (the W1W2 domains) linked to a unique 45-amino-acid C-terminal sequence (the Y1Y2 domain). This protein is highly expressed along with a second nuclear antigen, EBNA-2, during the initial stages of virus-induced B-cell transformation. While EBNA-2's essential role in transformation as a transcriptional activatory is well documented, very little is known about EBNA-LP function except that recombinant viruses lacking the EBNA-LP Y1Y2 exons show reduced, but still detectable, transforming ability. This was taken as evidence that EBNA-LP plays an auxiliary role but is not essential for transformation. A recent study showed that EBNA-LP could cooperate with EBNA-2 in activating cyclin D2 transcription in resting B cells (A.J. Sinclair, L Palmero, G. Peters, and P.J. Farrell, EMBO J. 13:3321-3328, 1994). Here we report that EBNA-LP can also cooperate with EBNA-2 in up-regulating expression of the major EBV effector protein of B-cell transformation, latent membrane protein 1 (LMP1). In transient-transfection assays, EBNA-LP enhanced the level of EBNA-2-induced LMP1 expression by 5- to 10-fold in one Latency I Burkitt's lymphoma cell line, Eli-BL, and was absolutely required, along with EBNA-2, to induce LMP1 in a second line, Akata-BL. These changes in LMP1 protein expression appeared to be reflected at the transcriptional level. A study of EBNA-LP mutants showed that this cooperative function mapped to the W1W2 repeat domain rather than to Y1Y2. Because a Y1Y2-deleted form of EBNA-LP may therefore retain some aspects of wild-type function, the original data from virus recombinants leave open the possibility that EBNA-LP is actually an essential transforming gene.
DOI: 10.1099/0022-1317-76-10-2423
发表时间: 1995-10-01
影响因子: 3.8
作者:
SZEKELY, L;JIANG, WQ;RINGERTZ, N
通讯作者: RINGERTZ, N
编码 Epstein-Barr 病毒核蛋白的 mRNA 的核苷酸序列:可能的转录起始位点。
DOI: 10.1073/pnas.83.14.5096
发表时间: 1986
影响因子: 11.1
作者:
Sample,J;Hummel,M;Braun,D;Birkenbach,M;Kieff,E
通讯作者: Kieff,E
DOI: 10.1073/pnas.91.16.7568
发表时间: 1994-08-02
影响因子: 11.1
作者:
GROSSMAN, SR;JOHANNSEN, E;KIEFF, E
通讯作者: KIEFF, E
DOI: 10.1016/0042-6822(90)90027-o
发表时间: 1990-06-01
期刊: VIROLOGY
影响因子: 3.7
作者:
PETTI, L;SAMPLE, C;KIEFF, E
通讯作者: KIEFF, E
DOI: 10.1073/pnas.81.12.3806
发表时间: 1984-01-01
期刊: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES
影响因子: --
作者:
YATES, J;WARREN, N;SUGDEN, B
通讯作者: SUGDEN, B