Haishi S, Imai H, Hirai K, Igarashi A, Kato S
Department of Virology, Nagasaki University, Japan.
Acta Virol. 1989 Dec;33(6):497-503.
Vaccinia virus recombinants inserted with cDNA clones of Japanese encephalitis (JE) virus envelope glycoprotein (E) gene were constructed. The E gene product was detected in the recombinant virus-infected BHK21 cells by immunofluorescence (IF) and Western blotting. The intensity of IF observed was higher by the recombinant of the TK promoter--P7.5 promoter--inserted cDNA construct than by the P7.5 promoter--TK promoter--inserted cDNA construct. The E gene product was hardly detected by the recombinant carrying the TK promoter only upstream to the inserted cDNA, although the glycoprotein E mRNA had been transcribed.
构建了插入日本脑炎(JE)病毒包膜糖蛋白(E)基因cDNA克隆的痘苗病毒重组体。通过免疫荧光(IF)和蛋白质印迹法在重组病毒感染的BHK21细胞中检测到E基因产物。观察到的IF强度,TK启动子-P7.5启动子-插入cDNA构建体的重组体比P7.5启动子-TK启动子-插入cDNA构建体的更高。仅在插入cDNA上游携带TK启动子的重组体中几乎检测不到E基因产物,尽管糖蛋白E mRNA已经转录。