Chen G, Willems L, Portetelle D, Willard-Gallo K E, Burny A, Gheysen D, Kettmann R
Faculty of Agronomy, Gembloux, Belgium.
Virology. 1989 Nov;173(1):343-7. doi: 10.1016/0042-6822(89)90254-7.
The bovine leukemia virus (BLV) p34tax (also called tat, p34, XLOR gene product) is a 34-kDa polypeptide encoded in the 3'-terminal region of the virus. This protein is responsible for positive transcriptional trans-activation of promoter elements located within the BLV long-terminal repeat. We introduced the protein-coding region of BLV p34tax into the genome of the baculovirus Autographa californica nuclear polyhedrosis virus. After infection of the insect Spodoptera frugiperda (SF9) cell line, this recombinant strain of baculovirus produced approximately 100 to 150 mg of p34tax per 2 X 10(9) cells. This protein, when introduced into mammalian fibroblasts by using a cell-to-cell fusion technique, functionally trans-activated the BLV long-terminal repeat. Analysis of 32P-labeled proteins of SF9 cells expressing BLV tax by two-dimensional gel electrophoresis indicated that the BLV p34tax was phosphorylated.
牛白血病病毒(BLV)p34tax(也称为tat、p34、XLOR基因产物)是一种由病毒3'端区域编码的34 kDa多肽。该蛋白负责对位于BLV长末端重复序列内的启动子元件进行正向转录反式激活。我们将BLV p34tax的蛋白编码区导入了苜蓿银纹夜蛾核型多角体病毒的基因组中。在感染昆虫草地贪夜蛾(SF9)细胞系后,这种重组杆状病毒每2×10⁹个细胞可产生约100至150 mg的p34tax。当通过细胞间融合技术将该蛋白导入哺乳动物成纤维细胞时,它能功能性地反式激活BLV长末端重复序列。通过二维凝胶电泳对表达BLV tax的SF9细胞的³²P标记蛋白进行分析表明,BLV p34tax发生了磷酸化。