Witte Vanessa, Laffert Bernd, Rosorius Olaf, Lischka Peter, Blume Katja, Galler Gunther, Stilper Andrea, Willbold Dieter, D'Aloja Paola, Sixt Michael, Kolanus Johanna, Ott Melanie, Kolanus Waldemar, Schuler Gerold, Baur Andreas S
Department of Dermatology, University of Erlangen/Nürnberg, 91052 Erlangen, Germany.
Mol Cell. 2004 Jan 30;13(2):179-90. doi: 10.1016/s1097-2765(04)00004-8.
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.
人类免疫缺陷病毒(HIV)和猿猴免疫缺陷病毒(SIV)的Nef蛋白被认为通过在质膜上形成信号复合物来干扰T细胞激活信号。该复合物的组成和功能尚未完全了解。在此,我们报告Nef将多梳蛋白家族(PcG)蛋白Eed招募到细胞膜上,Eed迄今为止被认为是一种核因子和转录抑制因子。Nef诱导的Eed易位导致Tat依赖的HIV转录受到强烈刺激,这意味着从细胞核中去除Eed是Tat发挥最佳功能所必需的。与Nef的作用类似,整合素受体的激活将Eed招募到质膜上,也导致Tat/Nef介导的转录增强。我们的结果表明膜相关激活过程与转录去抑制之间存在联系,并证明了HIV如何利用这一机制。