Mazarin V, Gourdou I, Querat G, Sauze N, Audoly G, Vitu C, Russo P, Rousselot C, Filippi P, Vigne R
Laboratoire de Virologie, Faculté de Médecine Nord, Marseille, France.
Virology. 1990 Sep;178(1):305-10. doi: 10.1016/0042-6822(90)90410-s.
The 1.4-kb mRNA of visna lentivirus is expressed early during the lytic infection of sheep choroid plexus cell cultures. It encodes for visna early gene 1 (VEG1) product, since renamed rev gene product (or Rev), based on significant amino acid sequence homologies between this protein and the proteins of simian immunodeficiency virus of macaque and human immunodeficiency virus type 2. In this report, we examined the subcellular localization and time course appearance of the Rev protein in visna virus-infected cells. Immunoprecipitation assays of [35S]methionine-labeled cell lysates with antisera raised against the Rev protein revealed a polypeptide of 19 kDa (p19rev). This protein was predominant early in the viral replication cycle and accumulated preferentially in the cytoplasmic/membrane fraction of infected cells. Indirect immunofluorescence staining of infected cells confirmed the cytoplasmic location of visna Rev protein and could reveal in some stained cells a higher concentration of Rev at the cellular plasma membrane. The regulating protein, still present late in the viral lytic cycle, is packaged into mature viral particles along with the structural gag and env gene products.
维斯纳慢病毒1.4kb的mRNA在绵羊脉络丛细胞培养物的裂解感染早期表达。它编码维斯纳早期基因1(VEG1)产物,基于该蛋白质与猕猴猿猴免疫缺陷病毒和人类免疫缺陷病毒2型蛋白质之间显著的氨基酸序列同源性,后来将其重新命名为rev基因产物(或Rev)。在本报告中,我们研究了Rev蛋白在维斯纳病毒感染细胞中的亚细胞定位和出现的时间进程。用针对Rev蛋白产生的抗血清对[35S]甲硫氨酸标记的细胞裂解物进行免疫沉淀分析,发现了一种19kDa的多肽(p19rev)。该蛋白在病毒复制周期早期占主导地位,并优先在感染细胞的细胞质/膜部分积累。对感染细胞进行间接免疫荧光染色证实了维斯纳Rev蛋白的细胞质定位,并且在一些染色细胞中可以发现Rev在细胞质膜处浓度更高。这种调节蛋白在病毒裂解周期后期仍然存在,它与结构性gag和env基因产物一起被包装到成熟的病毒颗粒中。