Itohara S, Tomiyama T, Ushimi C, Sekikawa K
Laboratory of Biophysics, National Institute of Animal Health, Ibaraki, Japan.
J Gen Virol. 1988 Apr;69 ( Pt 4):797-804. doi: 10.1099/0022-1317-69-4-797.
Bovine leukaemia virus (BLV) induces syncytia in productively infected ovine and bovine monolayer cells. Expression of the env gene directly determines the syncytium-forming activity, since the expression of a cloned env gene directed by the simian virus 40 (SV40) early promoter efficiently induced syncytia in transfected ovine embryonic (OE) cells. However a BLV long terminal repeat (LTR)-directed expression plasmid (pLTRenv) failed to induce syncytia in transfected OE cells, suggesting insufficient promoter activity of the LTR sequences. To assess the role of the XBL genes, which are located in the 3' distal region of the genome, in viral gene expression we constructed SV40 early promoter-directed expression plasmids. These contained open reading frames (ORFs) in the XBL region, and were examined for syncytium-inducing activity by cotransfection with pLTRenv. The results suggest that both XBL-I (the longest ORF: x-lor) and XBL-II (a shorter overlapping ORF: x-sor) are trans-acting genes which cooperatively activate LTR-directed viral gene expression.
牛白血病病毒(BLV)在高效感染的绵羊和牛单层细胞中诱导形成多核巨细胞。env基因的表达直接决定了多核巨细胞形成活性,因为由猴病毒40(SV40)早期启动子指导的克隆env基因的表达能在转染的绵羊胚胎(OE)细胞中有效诱导多核巨细胞形成。然而,一个由BLV长末端重复序列(LTR)指导的表达质粒(pLTRenv)未能在转染的OE细胞中诱导多核巨细胞形成,这表明LTR序列的启动子活性不足。为了评估位于基因组3'远端区域的XBL基因在病毒基因表达中的作用,我们构建了由SV40早期启动子指导的表达质粒。这些质粒在XBL区域含有开放阅读框(ORF),并通过与pLTRenv共转染来检测其诱导多核巨细胞形成的活性。结果表明,XBL-I(最长的ORF:x-lor)和XBL-II(较短的重叠ORF:x-sor)都是反式作用基因,它们协同激活LTR指导的病毒基因表达。