Dayton E T, Konings D A, Lim S Y, Hsu R K, Butini L, Pantaleo G, Dayton A I
National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.
J Virol. 1993 May;67(5):2871-8. doi: 10.1128/JVI.67.5.2871-2878.1993.
As part of a general program investigating the mechanism of the Rev axis of human immunodeficiency virus type 1 (HIV-1) autoregulation, a series of proviral HIV-1 mutants which differ from the parental HXB2 strain at selected positions within the RRE were constructed. All of the mutations were designed to perturb the RRE by introducing local helix disruptions without altering the coding potential of the overlapping envelope open reading frame. Viral replication in various cell types was monitored by a cell supernatant reverse transcriptase assay and Northern (RNA blot) analysis. All proviral RRE mutants displayed at least some impairment in replication. However, the relative impairment varied drastically among the various cell types tested. This suggests that the RRE may contribute to cell-type-specific viral tropism.
作为一项研究人类免疫缺陷病毒1型(HIV-1)自身调节Rev轴机制的总体计划的一部分,构建了一系列原病毒HIV-1突变体,这些突变体在RRE内的选定位置与亲本HXB2菌株不同。所有突变的设计都是通过引入局部螺旋破坏来干扰RRE,而不改变重叠包膜开放阅读框的编码潜力。通过细胞上清液逆转录酶测定和Northern(RNA印迹)分析监测各种细胞类型中的病毒复制。所有原病毒RRE突变体在复制中均表现出至少一些损害。然而,在所测试的各种细胞类型中,相对损害差异很大。这表明RRE可能有助于细胞类型特异性病毒嗜性。