Laboratory of Human Retrovirology, Institut de Recherches Cliniques de Montréal (IRCM), Montreal, Quebec, Canada.
PLoS Pathog. 2010 Sep 2;6(9):e1001080. doi: 10.1371/journal.ppat.1001080.
HIV-1 Viral protein R (Vpr) induces a cell cycle arrest at the G2/M phase by activating the ATR DNA damage/stress checkpoint. Recently, we and several other groups showed that Vpr performs this activity by recruiting the DDB1-CUL4A (VPRBP) E3 ubiquitin ligase. While recruitment of this E3 ubiquitin ligase complex has been shown to be required for G2 arrest, the subcellular compartment where this complex forms and functionally acts is unknown. Herein, using immunofluorescence and confocal microscopy, we show that Vpr forms nuclear foci in several cell types including HeLa cells and primary CD4+ T-lymphocytes. These nuclear foci contain VPRBP and partially overlap with DNA repair foci components such as gamma-H2AX, 53BP1 and RPA32. While treatment with the non-specific ATR inhibitor caffeine or depletion of VPRBP by siRNA did not inhibit formation of Vpr nuclear foci, mutations in the C-terminal domain of Vpr and cytoplasmic sequestration of Vpr by overexpression of Gag-Pol resulted in impaired formation of these nuclear structures and defective G2 arrest. Consistently, we observed that G2 arrest-competent sooty mangabey Vpr could form these foci but not its G2 arrest-defective paralog Vpx, suggesting that formation of Vpr nuclear foci represents a critical early event in the induction of G2 arrest. Indeed, we found that Vpr could associate to chromatin via its C-terminal domain and that it could form a complex with VPRBP on chromatin. Finally, analysis of Vpr nuclear foci by time-lapse microscopy showed that they were highly mobile and stable structures. Overall, our results suggest that Vpr recruits the DDB1-CUL4A (VPRBP) E3 ligase to these nuclear foci and uses these mobile structures to target a chromatin-bound cellular substrate for ubiquitination in order to induce DNA damage/replication stress, ultimately leading to ATR activation and G2 cell cycle arrest.
HIV-1 病毒蛋白 R(Vpr)通过激活 ATR 损伤/应激检查点,将细胞周期阻滞在 G2/M 期。最近,我们和其他几个小组表明,Vpr 通过招募 DDB1-CUL4A(VPRBP)E3 泛素连接酶来发挥这种作用。虽然已经表明该 E3 泛素连接酶复合物的募集对于 G2 期阻滞是必需的,但该复合物形成和发挥功能的亚细胞区室尚不清楚。在此,我们使用免疫荧光和共聚焦显微镜,显示 Vpr 在包括 HeLa 细胞和原代 CD4+T 淋巴细胞在内的几种细胞类型中形成核斑点。这些核斑点包含 VPRBP,并且与 DNA 修复斑点成分如γ-H2AX、53BP1 和 RPA32 部分重叠。虽然用非特异性 ATR 抑制剂咖啡因处理或 siRNA 耗尽 VPRBP 不会抑制 Vpr 核斑点的形成,但 Vpr C 末端结构域的突变和 Gag-Pol 的过度表达导致这些核结构的形成受损和 G2 期阻滞缺陷。一致地,我们观察到具有 G2 期阻滞能力的食蟹猴 Vpr 可以形成这些斑点,但缺乏 G2 期阻滞缺陷的 Vpx 则不能,这表明 Vpr 核斑点的形成代表了诱导 G2 期阻滞的一个关键早期事件。事实上,我们发现 Vpr 可以通过其 C 末端结构域与染色质结合,并且它可以在染色质上与 VPRBP 形成复合物。最后,通过延时显微镜分析 Vpr 核斑点,发现它们是高度移动和稳定的结构。总体而言,我们的结果表明,Vpr 将 DDB1-CUL4A(VPRBP)E3 连接酶招募到这些核斑点,并利用这些可移动结构来靶向染色质结合的细胞底物进行泛素化,从而诱导 DNA 损伤/复制应激,最终导致 ATR 激活和 G2 细胞周期阻滞。