Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94158, USA.
Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94158, USA.
Sci Adv. 2024 Jan 19;10(3):eadi4162. doi: 10.1126/sciadv.adi4162.
The Tat proteins of HIV-1 and simian immunodeficiency virus (SIV) are essential for activating viral transcription. In addition, Tat stimulates nuclear factor κB (NF-κB) signaling pathways to regulate viral gene expression although its molecular mechanism is unclear. Here, we report that Tat directly activates NF-κB through the interaction with TRAF6, which is an essential upstream signaling molecule of the canonical NF-κB pathway. This interaction increases TRAF6 oligomerization and auto-ubiquitination, as well as the synthesis of K63-linked polyubiquitin chains to further activate the NF-κB pathway and HIV-1 transcription. Moreover, ectopic expression of TRAF6 significantly activates HIV-1 transcription, whereas TRAF6 knockdown inhibits transcription. Furthermore, Tat-mediated activation of NF-κB through TRAF6 is conserved among HIV-1, HIV-2, and SIV isolates. Our study uncovers yet another mechanism by which HIV-1 subverts host transcriptional pathways to enhance its own transcription.
HIV-1 和猴免疫缺陷病毒(SIV)的 Tat 蛋白对于激活病毒转录至关重要。此外,尽管其分子机制尚不清楚,但 Tat 通过与 TRAF6 的相互作用刺激核因子 κB(NF-κB)信号通路来调节病毒基因表达,TRAF6 是经典 NF-κB 途径的必需上游信号分子。本研究报告称,Tat 通过与 TRAF6 相互作用直接激活 NF-κB,这种相互作用会增加 TRAF6 的寡聚化和自身泛素化,以及合成 K63 连接的多泛素链,从而进一步激活 NF-κB 途径和 HIV-1 转录。此外,TRAF6 的异位表达可显著激活 HIV-1 转录,而 TRAF6 的敲低则抑制转录。此外,Tat 通过 TRAF6 介导的 NF-κB 激活在 HIV-1、HIV-2 和 SIV 分离株中是保守的。本研究揭示了 HIV-1 颠覆宿主转录途径以增强自身转录的另一种机制。