Lu A, Miller L K
Department of Entomology, University of Georgia, Athens 30602-2603.
J Virol. 1994 Oct;68(10):6710-8. doi: 10.1128/JVI.68.10.6710-6718.1994.
A transient transactivation assay system was used in combination with an overlapping Autographa californica nuclear polyhedrosis virus clone library to identify genes involved in late and very late baculovirus gene expression. We have identified three genes within the 33.8- to 43.4-map-unit region of the A. californica nuclear polyhedrosis virus genome which contribute to expression from promoters of the vp39 major capsid protein and polyhedrin genes. One of these three genes corresponds to the previously identified DNA polymerase gene, while the other two genes encode previously unidentified polypeptides of 59,418 and 8,706 Da. None of these genes were required for expression from the early etl promoter.
使用瞬时反式激活检测系统与一个重叠的苜蓿银纹夜蛾核型多角体病毒克隆文库相结合,以鉴定参与杆状病毒晚期和极晚期基因表达的基因。我们在苜蓿银纹夜蛾核型多角体病毒基因组的33.8至43.4图谱单位区域内鉴定出三个基因,这些基因有助于vp39主要衣壳蛋白和多角体蛋白基因启动子的表达。这三个基因中的一个对应于先前鉴定的DNA聚合酶基因,而另外两个基因编码先前未鉴定的59418和8706 Da的多肽。早期etl启动子的表达不需要这些基因中的任何一个。