Division of Cell Biology and Immunology, Department of Pathology, University of Utah School of Medicine, 15 North Medical Drive East #2100-Room 2520, Salt Lake City, Utah 84112, USA.
Curr Top Microbiol Immunol. 2009;339:177-200. doi: 10.1007/978-3-642-02175-6_9.
Like most viral regulatory proteins, HIV-1 Vpr and homologous proteins from primate lentiviruses are small and multifunctional. They are associated with a plethora of effects and functions, including induction of cell cycle arrest in the G(2) phase, induction of apoptosis, transactivation, enhancement of the fidelity of reverse transcription, and nuclear import of viral DNA in macrophages and other nondividing cells. This review focuses on the cellular proteins that have been reported to interact with Vpr and their significance with respect to the known functions and effects of Vpr on cells and on viral replication.
与大多数病毒调节蛋白一样,HIV-1 Vpr 和灵长类慢病毒的同源蛋白体积小且多功能。它们与多种作用和功能相关,包括诱导 G2 期细胞周期停滞、诱导细胞凋亡、反式激活、提高逆转录保真度以及在巨噬细胞和其他非分裂细胞中导入病毒 DNA。这篇综述重点介绍了已报道与 Vpr 相互作用的细胞蛋白,以及它们对 Vpr 已知功能和对细胞及病毒复制的影响的意义。