Self-inhibition of synthesis and antigen presentation by Epstein-Barr virus-encoded EBNA1

被引:211
作者
Yin, Y
Manoury, B
Fåhraeus, R [1 ]
机构
[1] Univ Dundee, Fac Life Sci, Div Mol Physiol, Dundee DD1 5EH, Scotland
[2] Univ Dundee, Fac Life Sci, Div Cell Biol & Immunol, Dundee DD1 5EH, Scotland
关键词
D O I
10.1126/science.1088902
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The glycine-alanine repeat domain (GAr) of Epstein-Barr virus-encoded nuclear antigen 1 (EBNA1) prevents major histocompatibility complex (MHC) class I restricted presentation of EBNA1 epitopes to cytotoxic T cells. This effect has previously been attributed to the ability of GAr to inhibit its own proteasomal degradation. Here we show, both in vitro and in vivo, that GAr also inhibits messenger RNA translation of EBNA1 in cis and that this effect can be distinguished from its effect on proteasomal degradation. Hence, inhibition of messenger RNA translation, but not protein degradation, is essential to prevent antigen presentation on MHC class I molecules. Thus, by minimizing translation of the EBNA1 transcript, cells expressing EBNA1 avoid cytotoxic T cell recognition. At the same time, blocking degradation maintains the EBNA1 expression level.
引用
收藏
页码:1371 / 1374
页数:4
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