Markovitz D M, Kenney S, Kamine J, Smith M S, Davis M, Huang E S, Rosen C, Pagano J S
Department of Medicine, University of North Carolina, Chapel Hill 27599.
Virology. 1989 Dec;173(2):750-4. doi: 10.1016/0042-6822(89)90591-6.
The BMLF1 region of the Epstein-Barr virus (EBV) genome and the immediate-early (IE) region of human cytomegalovirus (HCMV) both encode proteins which can trans-activate heterologous promoter/chloramphenicol acetyl transferase (CAT) constructs, including a human immunodeficiency virus type-1 promoter/CAT construct. We demonstrate here that this trans-activation by the EBV BMLF1 gene product, which we have previously shown to be largely post-transcriptional, is reporter gene dependent. In contrast, trans-activation by the HCMV-IE gene product(s), previously shown to be mediated at the RNA level, is seen regardless of whether CAT, human growth hormone, or beta-galactosidase is used as the reporter gene. Mutational analysis revealed no specific cis-acting sequences within the HIV-1 promoter which were required for trans-activation by the HCMV-IE gene product(s).
爱泼斯坦-巴尔病毒(EBV)基因组的BMLF1区域和人巨细胞病毒(HCMV)的立即早期(IE)区域均编码能反式激活异源启动子/氯霉素乙酰转移酶(CAT)构建体的蛋白质,包括1型人类免疫缺陷病毒启动子/CAT构建体。我们在此证明,EBV BMLF1基因产物的这种反式激活作用(我们之前已表明其主要发生在转录后水平)依赖于报告基因。相比之下,HCMV-IE基因产物的反式激活作用(之前已表明其在RNA水平介导),无论使用CAT、人生长激素还是β-半乳糖苷酶作为报告基因均可观察到。突变分析显示,HIV-1启动子内不存在HCMV-IE基因产物反式激活所需的特定顺式作用序列。