Carbonell L F, Hodge M R, Tomalski M D, Miller L K
Department of Genetics, University of Georgia, Athens 30602.
Gene. 1988 Dec 20;73(2):409-18. doi: 10.1016/0378-1119(88)90505-7.
We have explored the possibility of improving baculovirus pesticides by incorporating an insect-specific neurotoxin gene into a baculovirus genome. A 112-bp gene (BeIt) encoding insectotoxin-1 of the scorpion Buthus eupeus was synthesized and cloned in Escherichia coli. For expression, BeIt was transferred to the DNA genome of Autographa californica nuclear polyhedrosis virus (AcMNPV). Three different recombinant AcMNPVs, carrying BeIt under the control of the strong AcMNPV polyhedrin promoter, were constructed and expression of BeIt was monitored upon infection of Spodoptera frugiperda (Sf) cells. Toxin expression was low using a recombinant virus in which BeIt was inserted 6 nucleotides (nt) downstream from the intact polyhedrin mRNA leader. More expression was observed when a signal-peptide was attached in-frame to the N terminus of BeIt. The highest level of expression was observed with a fusion gene comprised of the 58 N-terminal codons of polyhedrin fused to BeIt; however, the level of expression was ten- to twenty-fold below that for polyhedrin. Polyhedrin promoter-directed transcripts of all three recombinants accumulated to levels similar to those of wild-type polyhedrin transcripts, indicating that the limitation to expression of unfused BeIt was not at the level of transcription but rather at the posttranscriptional level including translation or protein stability. Paralytic activity of the toxin products was not detected.
我们探索了通过将昆虫特异性神经毒素基因整合到杆状病毒基因组中来改进杆状病毒杀虫剂的可能性。合成了一个编码蝎子东亚钳蝎昆虫毒素-1的112碱基对基因(BeIt),并将其克隆到大肠杆菌中。为了进行表达,将BeIt转移到苜蓿银纹夜蛾核型多角体病毒(AcMNPV)的DNA基因组中。构建了三种不同的重组AcMNPV,它们在强AcMNPV多角体蛋白启动子的控制下携带BeIt,并在感染草地贪夜蛾(Sf)细胞后监测BeIt的表达。使用一种重组病毒时毒素表达较低,在这种重组病毒中,BeIt插入到完整多角体蛋白mRNA前导序列下游6个核苷酸(nt)处。当一个信号肽与BeIt的N端框内连接时,观察到更多的表达。在由多角体蛋白的58个N端密码子与BeIt融合组成的融合基因中观察到最高水平的表达;然而,表达水平比多角体蛋白低10到20倍。所有三种重组体的多角体蛋白启动子指导的转录本积累到与野生型多角体蛋白转录本相似的水平,这表明未融合的BeIt表达的限制不在转录水平,而是在转录后水平,包括翻译或蛋白质稳定性。未检测到毒素产物的麻痹活性。