Guarino Linda A, Mistretta Toni-Ann, Dong Wen
Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas 77843-2128, USA.
J Virol. 2002 Dec;76(23):12032-43. doi: 10.1128/jvi.76.23.12032-12043.2002.
The baculovirus lef-12 (orf41) gene is required for transient expression of baculovirus late genes. To analyze the role of LEF-12 in the context of infected cells, two mutant viruses were constructed. Both mutants were viable in Trichoplusia ni High 5 and Spodoptera frugiperda Sf9 cells. Single-step growth curves, however, indicated that virus yields were reduced approximately fivefold in the absence of LEF-12. Pulse-labeling of infected cells revealed that LEF-12 mutant viruses entered the late phase and synthesized late proteins at levels equivalent to or only twofold lower than those of wild-type virus-infected cells. Western blot analyses confirmed that LEF-12 was not synthesized in cells infected with mutant virus. In wild-type virus-infected cells, LEF-12 was not detected until 18 h postinfection, and accumulation of LEF-12 peaked at 24 to 36 h postinfection. Primer extension mapping revealed that lef-12 mRNA was synthesized by 12 h postinfection and peaked between 18 and 24 h postinfection. Furthermore, synthesis of lef-12 mRNA and LEF-12 protein were inhibited by the addition of aphidicolin, indicating that lef-12 is expressed after DNA replication.
杆状病毒lef - 12(orf41)基因是杆状病毒晚期基因瞬时表达所必需的。为了分析LEF - 12在被感染细胞中的作用,构建了两种突变病毒。这两种突变体在粉纹夜蛾High 5细胞和草地贪夜蛾Sf9细胞中均能存活。然而,单步生长曲线表明,在没有LEF - 12的情况下,病毒产量降低了约五倍。对被感染细胞进行脉冲标记显示,LEF - 12突变病毒进入晚期阶段,并合成晚期蛋白,其水平与野生型病毒感染细胞相当或仅低两倍。蛋白质免疫印迹分析证实,在感染突变病毒的细胞中未合成LEF - 12。在野生型病毒感染的细胞中,直到感染后18小时才检测到LEF - 12,并且LEF - 12的积累在感染后24至36小时达到峰值。引物延伸图谱显示,lef - 12 mRNA在感染后12小时合成,并在感染后18至24小时达到峰值。此外,添加阿非迪霉素可抑制lef - 12 mRNA和LEF - 12蛋白的合成,这表明lef - 12在DNA复制后表达。