Guenzel Carolin A, Hérate Cécile, Benichou Serge
Cochin Institute, INSERM U1016, Centre National de la Recherche Scientifique UMR8104, Université Paris-Descartes Paris, France.
Front Microbiol. 2014 Mar 31;5:127. doi: 10.3389/fmicb.2014.00127. eCollection 2014.
Like other HIV-1 auxiliary proteins, Vpr is conserved within all the human (HIV-1, HIV-2) and simian (SIV) immunodeficiency viruses. However, Vpr and homologous HIV-2, and SIV Vpx are the only viral auxiliary proteins specifically incorporated into virus particles through direct interaction with the Gag precursor, indicating that this presence in the core of the mature virions is mainly required for optimal establishment of the early steps of the virus life cycle in the newly infected cell. In spite of its small size, a plethora of effects and functions have been attributed to Vpr, including induction of cell cycle arrest and apoptosis, modulation of the fidelity of reverse transcription, nuclear import of viral DNA in macrophages and other non-dividing cells, and transcriptional modulation of viral and host cell genes. Even if some more recent studies identified a few cellular targets that HIV-1 Vpr may utilize in order to perform its different tasks, the real role and functions of Vpr during the course of natural infection are still enigmatic. In this review, we will summarize the main reported functions of HIV-1 Vpr and their significance in the context of the viral life cycle.
与其他HIV-1辅助蛋白一样,Vpr在所有人类(HIV-1、HIV-2)和猿猴(SIV)免疫缺陷病毒中都具有保守性。然而,Vpr以及同源的HIV-2和SIV Vpx是仅有的通过与Gag前体直接相互作用而特异性掺入病毒颗粒的病毒辅助蛋白,这表明成熟病毒粒子核心中的这种存在对于在新感染细胞中最佳地建立病毒生命周期早期步骤主要是必需的。尽管Vpr体积小,但它具有多种效应和功能,包括诱导细胞周期停滞和凋亡、调节逆转录保真度、促进病毒DNA在巨噬细胞和其他非分裂细胞中的核输入以及调节病毒和宿主细胞基因的转录。即使最近的一些研究确定了HIV-1 Vpr可能用于执行其不同任务的一些细胞靶点,但Vpr在自然感染过程中的真正作用和功能仍然是个谜。在本综述中,我们将总结HIV-1 Vpr的主要报道功能及其在病毒生命周期中的意义。