Sakai H, Shibata R, Miura T, Hayami M, Ogawa K, Kiyomasu T, Ishimoto A, Adachi A
Department of Viral Oncology, Kyoto University, Japan.
J Virol. 1990 May;64(5):2202-7. doi: 10.1128/JVI.64.5.2202-2207.1990.
The functional exchangeability of the rev gene was assessed in transient transfection experiments by using in vitro-constructed rev and gag mutants of the following three primate lentiviruses: human immunodeficiency virus type 1 (HIV-1), HIV-2, and simian immunodeficiency virus from the African green monkey (SIV AGM). Cotransfection into SW480 cells of the rev and gag mutants derived from the DNA of each infectious virus resulted in the generation of progeny particles as determined by reverse transcriptase assay. rev gene mutants of HIV-2 and SIV AGM were also complemented by all gag mutants derived from the three viruses. In contrast, no evidence of complementation was obtained following cotransfection of the HIV-1 rev mutant and the gag mutant of HIV-2 or SIV AGM.
通过使用体外构建的以下三种灵长类慢病毒的rev和gag突变体,在瞬时转染实验中评估rev基因的功能互换性:1型人类免疫缺陷病毒(HIV-1)、HIV-2以及来自非洲绿猴的猴免疫缺陷病毒(SIV AGM)。将源自每种感染性病毒DNA的rev和gag突变体共转染到SW480细胞中,通过逆转录酶测定确定产生了子代颗粒。HIV-2和SIV AGM的rev基因突变体也被源自这三种病毒的所有gag突变体所互补。相比之下,HIV-1 rev突变体与HIV-2或SIV AGM的gag突变体共转染后,未获得互补的证据。