Beames B, Summers M D
Department of Entomology, Texas A&M Unitersity, College Station, Texas 77843-2475.
Virology. 1988 Jan;162(1):206-20. doi: 10.1016/0042-6822(88)90410-2.
Few polyhedgra (FP) mutants of Autographa californica nuclear polyhedrosis virus (AcNPV) and the closely related strain Galleria mellonella (Gm)NPV have been reported which contain Trichoplusia ni host cell DNA sequences inserted into the viral genome between map units 35.0 and 37.7. New FP mutants are described with alterations of the HindIII-I restriction enzyme fragment (33.8 to 37.7 map units) of AcNPV, either deletions of viral DNA sequences or insertions of spodoptera frugiperda host cell DNA sequences. S. frugiperda DNA insertions from FP mutants were compared to T. ni host DNA insertions from FP mutants previously isolated (M.J. Fraser, G.E. Smith, and M.D. Summers (1983) J. Virol. 47, 287-300). Two host cell DNA sequences isolated from FP mutants, one of T. ni origin and one from S. frugiperda DNA, were transcribed in infected cells. Deletions of viral DNA sequences and insertions of host DNA sequences produce altered transcripts at the site of mutation as determined by both Northern and S1 nuclease analysis. Cell-free translation of cRNAs transcribed from wild-type viral DNA revealed an open reading frame coding for a 25-kDa protein at the site where host cell DNA insertions have been mapped. This was the same size as an infected-cell protein missing from most FP mutants examined.
已报道了苜蓿银纹夜蛾核型多角体病毒(AcNPV)以及密切相关的菌株大蜡螟(Gm)NPV的少数多面体(FP)突变体,这些突变体包含插入到病毒基因组中位于图谱单位35.0至37.7之间的粉纹夜蛾宿主细胞DNA序列。本文描述了新的FP突变体,其具有AcNPV的HindIII-I限制性酶切片段(图谱单位33.8至37.7)的改变,要么是病毒DNA序列的缺失,要么是草地贪夜蛾宿主细胞DNA序列的插入。将来自FP突变体的草地贪夜蛾DNA插入片段与先前分离的来自FP突变体的粉纹夜蛾宿主DNA插入片段(M.J.弗雷泽、G.E.史密斯和M.D.萨默斯(1983年)《病毒学杂志》47卷,287 - 300页)进行了比较。从FP突变体中分离出的两个宿主细胞DNA序列,一个源自粉纹夜蛾,另一个来自草地贪夜蛾DNA,在受感染细胞中被转录。通过Northern印迹分析和S1核酸酶分析确定,病毒DNA序列的缺失和宿主DNA序列的插入在突变位点产生了改变的转录本。从野生型病毒DNA转录的cRNAs的无细胞翻译揭示,在宿主细胞DNA插入位点映射到的位置有一个编码25 kDa蛋白质的开放阅读框。这与大多数所检测的FP突变体中缺失的一种感染细胞蛋白大小相同。