Pizzella T, Banerjee R
Department of Biochemistry, Mount Sinai School of Medicine, New York, NY 10029.
DNA Cell Biol. 1994 Jan;13(1):67-74. doi: 10.1089/dna.1994.13.67.
Recently, we have shown that the human immunodeficiency virus (HIV-1) long terminal repeat (LTR) directed chloramphenicol acetyltransferase (CAT) gene is efficiently expressed in human hepatoblastoma HepG2 cells and these cells can support productive HIV-1 replication. In this study we show that HepG2 cells contain a nuclear factor that binds to the HIV-1 trans-activating region (TAR), which we named HepG2-derived TAR binding protein (HTBP). Gel retardation assays using synthetic oligonucleotide probes carrying different mutations in the TAR region and competition DNA mobility-shift experiments using these oligonucleotides revealed the binding site encompassing between +7 and +13 nucleotides (5'-TCTGGTT-3') in the HIV-1 LTR. An in vivo CAT competition assay using -65HIV-1 LTR CAT as a reporter plasmid and various competitor plasmids containing these mutated oligonucleotides also demonstrated that HTBP can influence the HIV-1 LTR-directed CAT gene expression in HepG2 cells by interaction with a specific sequence in the TAR region.
最近,我们已经表明,人类免疫缺陷病毒(HIV-1)长末端重复序列(LTR)指导的氯霉素乙酰转移酶(CAT)基因在人肝癌HepG2细胞中高效表达,并且这些细胞能够支持HIV-1的有效复制。在本研究中,我们发现HepG2细胞含有一种与HIV-1反式激活区(TAR)结合的核因子,我们将其命名为HepG2来源的TAR结合蛋白(HTBP)。使用在TAR区域携带不同突变的合成寡核苷酸探针进行的凝胶阻滞试验,以及使用这些寡核苷酸进行的竞争DNA迁移率变动实验,揭示了HIV-1 LTR中包含第+7至+13个核苷酸(5'-TCTGGTT-3')之间的结合位点。使用-65HIV-1 LTR CAT作为报告质粒以及包含这些突变寡核苷酸的各种竞争质粒进行的体内CAT竞争试验也表明,HTBP可以通过与TAR区域中的特定序列相互作用来影响HepG2细胞中HIV-1 LTR指导下的CAT基因表达。