Sakuragi J, Sakai H, Sakuragi S, Shibata R, Wain-Hobson S, Hayami M, Adachi A
Department of Virai Oncology, Kyoto University, Japan.
Virology. 1992 Jul;189(1):354-8. doi: 10.1016/0042-6822(92)90715-2.
In reporter-based transient expression systems, we characterized simian immunodeficiency virus from a chimpanzee (SIVCPZ), with special reference to the human immunodeficiency virus type 1 (HIV-1). SIVCPZ was not equally activated by tat and rev transactivators derived from representative primate lentiviruses. HIV-1 alone activated SIVCPZ to the full extent in both tat and rev assays. The tat and rev gene products of SIVCPZ, as well as those of HIV-1, efficiently transactivated the other viruses. These results indicate that SIVCPZ is identical to HIV-1 with regard to the compatibility of tat and rev gene activities among four subgroups of primate lentiviruses.
在基于报告基因的瞬时表达系统中,我们对来自黑猩猩的猿猴免疫缺陷病毒(SIVCPZ)进行了特性分析,特别参照了1型人类免疫缺陷病毒(HIV-1)。源自代表性灵长类慢病毒的tat和rev反式激活因子对SIVCPZ的激活效果并不相同。仅HIV-1在tat和rev检测中均能将SIVCPZ完全激活。SIVCPZ以及HIV-1的tat和rev基因产物均能有效地反式激活其他病毒。这些结果表明,在灵长类慢病毒的四个亚组中,就tat和rev基因活性的兼容性而言,SIVCPZ与HIV-1是相同的。