Joseph Ajith Mathew, Ladha Jayashree S, Mojamdar Manoj, Mitra Debashis
National Centre for Cell Science, Ganeshkhind, Pune 411007, India.
FEBS Lett. 2003 Jul 31;548(1-3):37-42. doi: 10.1016/s0014-5793(03)00725-7.
The human immunodeficiency virus (HIV-1) Nef protein is now regarded as a regulatory protein responsible not only for establishment of infection and increased pathogenesis but also for enhancement of viral replication. However, the mechanism of Nef-induced activation of viral replication remains to be clearly understood. Using transient transfection assay, co-immunoprecipitation and pull-down analysis, we demonstrate in this report that the HIV-1 Nef protein physically interacts with Tat, the principal transactivating protein of HIV-1. Our observations with single cycle replication experiments further indicate that this interaction results not only in enhancement of Tat-induced HIV-1 long terminal repeat-mediated gene expression but also in virus production.
人类免疫缺陷病毒1型(HIV-1)Nef蛋白现在被视为一种调节蛋白,不仅负责感染的建立和发病机制的增强,还负责促进病毒复制。然而,Nef诱导病毒复制激活的机制仍有待明确。在本报告中,我们通过瞬时转染试验、免疫共沉淀和下拉分析证明,HIV-1 Nef蛋白与HIV-1的主要反式激活蛋白Tat发生物理相互作用。我们单周期复制实验的观察结果进一步表明,这种相互作用不仅导致Tat诱导的HIV-1长末端重复序列介导的基因表达增强,还导致病毒产生。