共 42 条
RBP-J kappa repression activity is mediated by a co-repressor and antagonized by the Epstein-Barr virus transcription factor EBNA2
被引:73
作者:

Waltzer, L
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h-index: 0
机构: Unit de Virologie Humaine, ENS-INSERM U412, Ecole Normale Supeèrieure de Lyon, 69364 Lyon Cedex 07

Bourillot, PY
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h-index: 0
机构: Unit de Virologie Humaine, ENS-INSERM U412, Ecole Normale Supeèrieure de Lyon, 69364 Lyon Cedex 07

Sergeant, A
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机构: Unit de Virologie Humaine, ENS-INSERM U412, Ecole Normale Supeèrieure de Lyon, 69364 Lyon Cedex 07

Manet, E
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h-index: 0
机构: Unit de Virologie Humaine, ENS-INSERM U412, Ecole Normale Supeèrieure de Lyon, 69364 Lyon Cedex 07
机构:
[1] Unit de Virologie Humaine, ENS-INSERM U412, Ecole Normale Supeèrieure de Lyon, 69364 Lyon Cedex 07
关键词:
D O I:
10.1093/nar/23.24.4939
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 Epstein-Barr virus (EBV) protein EBNA2 is a transcriptional activator that can be targeted to its DNA responsive elements by direct interaction with the cellular protein RBP-J kappa. RBP-J kappa is a ubiquitous factor, highly conserved between man, mouse and Drosophila, whose function in mammalian cells is largely unknown, Here we provide evidence that RBP-J kappa is a transcriptional repressor and, more importantly, that RBP-J kappa repression is mediated by a co-repressor, The function of the cc-repressor could be counterbalanced by making a fusion protein (RBP-VP16) between RBP-J kappa and the VP16 activation domain, This RBP-VP16-mediated activation could be strongly increased by an EBNA2 protein deprived of its activation domain, but not by an EBNA2 protein incapable of making physical contact with RBP-J kappa. Our results suggest that EBNA2 activates transcription by both interfering with the function of a co-repressor recruited by RBP-J kappa and providing an activation domain.
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页码:4939 / 4945
页数:7
相关论文
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