Pomerantz R J, Seshamma T, Trono D
Department of Medicine, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.
J Virol. 1992 Mar;66(3):1809-13. doi: 10.1128/JVI.66.3.1809-1813.1992.
The Rev protein of human immunodeficiency virus type 1 (HIV-1) is essential for the expression of the structural genes of HIV-1. To determine whether a functional threshold level of Rev is required to allow efficient HIV-1 replication, CD4-positive HeLa cells, constitutively expressing a Rev-deficient provirus, were transfected with various quantities of a Rev-expressing plasmid. Compared with the quantity of the Rev-producing plasmid transfected, HIV-1 replication was distinctly nonlinear as measured by HIV-1 p24 antigen and HIV-1-specific RNA production. A quantitative RNA polymerase chain reaction (PCR) demonstrated that Rev mRNA expression was linearly correlated with the quantity of Rev-expressing plasmid which was transfected into these cells. These data suggest that a critical threshold of Rev is required for a highly productive HIV-1 infection. This threshold level of Rev may be involved in the generation and maintenance of HIV-1 proviral latency.
人类免疫缺陷病毒1型(HIV-1)的Rev蛋白对于HIV-1结构基因的表达至关重要。为了确定是否需要Rev的功能阈值水平以允许高效的HIV-1复制,将持续表达Rev缺陷型前病毒的CD4阳性HeLa细胞用不同量的Rev表达质粒进行转染。与转染的Rev产生质粒的量相比,通过HIV-1 p24抗原和HIV-1特异性RNA产生来测量,HIV-1复制明显呈非线性。定量RNA聚合酶链反应(PCR)表明,Rev mRNA表达与转染到这些细胞中的Rev表达质粒的量呈线性相关。这些数据表明,高效的HIV-1感染需要Rev的临界阈值。Rev的这个阈值水平可能参与HIV-1前病毒潜伏期的产生和维持。