Malim M H, Böhnlein S, Fenrick R, Le S Y, Maizel J V, Cullen B R
Howard Hughes Medical Institute, Duke University Medical Center, Durham, NC 27710.
Proc Natl Acad Sci U S A. 1989 Nov;86(21):8222-6. doi: 10.1073/pnas.86.21.8222.
The known primate lentiviruses can be divided into two subgroups consisting of the human immunodeficiency virus type 1 (HIV-1) isolates and the related HIV type 2 (HIV-2) and simian immunodeficiency virus (SIV) isolates. HIV-1 has been shown to encode a post-transcriptional trans-activator of viral structural gene expression, termed Rev, that is essential for viral replication in culture. Here, we demonstrate that HIV-2 and SIVmac also encode functional Rev proteins. As in the case of HIV-1, these Rev trans-activators are shown to induce the cytoplasmic expression of the unspliced viral transcripts that encode the viral structural proteins. Unexpectedly, the Rev proteins of HIV-2 and SIVmac proved incapable of activating the cytoplasmic expression of unspliced HIV-1 transcripts, whereas HIV-1 Rev was fully functional in the HIV-2/SIV system. This nonreciprocal complementation may imply a direct role for Rev in mediating the recognition of its viral RNA target sequence.
已知的灵长类慢病毒可分为两个亚组,一组由1型人类免疫缺陷病毒(HIV-1)分离株组成,另一组由相关的2型HIV(HIV-2)和猴免疫缺陷病毒(SIV)分离株组成。已证明HIV-1编码一种病毒结构基因表达的转录后反式激活因子,称为Rev,它对于病毒在培养中的复制至关重要。在此,我们证明HIV-2和SIVmac也编码功能性Rev蛋白。与HIV-1的情况一样,这些Rev反式激活因子可诱导编码病毒结构蛋白的未剪接病毒转录本在细胞质中表达。出乎意料的是,HIV-2和SIVmac的Rev蛋白无法激活未剪接的HIV-1转录本的细胞质表达,而HIV-1 Rev在HIV-2/SIV系统中功能完全正常。这种非相互互补可能意味着Rev在介导其病毒RNA靶序列识别中起直接作用。