AI Article Synopsis

  • Nef protein from HIV/SIV disrupts T cell activation by forming a signaling complex at the plasma membrane, though its full composition and function are unclear.
  • Nef recruits the Polycomb Group protein Eed to the cell membrane, which enhances Tat-dependent HIV transcription by removing Eed from the nucleus.
  • This study reveals how HIV uses membrane-associated processes to boost transcription, linking receptor activation to transcriptional changes.

Article Abstract

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.

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Source
http://dx.doi.org/10.1016/s1097-2765(04)00004-8DOI Listing

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