HIV-1 Nef mimics an integrin receptor signal that recruits the polycomb group protein Eed to the plasma membrane

被引:71
作者
Witte, V
Laffert, B
Rosorius, O
Lischka, P
Blume, K
Galler, G
Stilper, A
Willbold, D
D'Aloja, P
Sixt, M
Kolanus, J
Ott, M
Kolanus, W
Schuler, G
Baur, AS
机构
[1] Univ Erlangen Nurnberg, Dept Dermatol, D-91052 Erlangen, Germany
[2] Univ Erlangen Nurnberg, Dept Physiol Chem, D-91052 Erlangen, Germany
[3] Univ Erlangen Nurnberg, Inst Clin & Mol Virol, D-91052 Erlangen, Germany
[4] Nikolaus Fiebiger Ctr Mol Med, D-91054 Erlangen, Germany
[5] Univ Dusseldorf, Inst Phys Biol, D-52425 Julich, Germany
[6] Inst Expt Pathol, S-22362 Lund, Sweden
[7] Univ Bonn, Inst Mol Physiol & Dev Biol, D-53115 Bonn, Germany
[8] Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94103 USA
关键词
D O I
10.1016/S1097-2765(04)00004-8
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 Nef protein of human and simian immunodeficiency virus (HIV/SIV) is believed to interfere with T cell activation signals by forming a signaling complex at the plasma membrane. Composition and function of the complex are not fully understood. Here we report that Nef recruits the Polycomb Group (PcG) protein Eed, so far known as a nuclear factor and repressor of transcription, to the membrane of cells. The Nef-induced translocation of Eed led to a potent stimulation of Tat-dependent HIV transcription, implying that Eed removal from the nucleus is required for optimal Tat function. Similar to Nef action, activation of integrin receptors recruited Eed to the plasma membrane, also leading to enhanced Tat/Nef-mediated transcription. Our results suggest a link between membrane-associated activation processes and transcriptional derepression and demonstrate how HIV exploits this mechanism.
引用
收藏
页码:179 / 190
页数:12
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