Lu A, Carstens E B
Department of Microbiology and Immunology, Queen's University, Kingston, Ontario, Canada.
Virology. 1992 Sep;190(1):201-9. doi: 10.1016/0042-6822(92)91206-a.
The 67.2- to 68.5-m.u. region of Autographa californica nuclear polyhedrosis virus was sequenced. A large open reading frame (ORF) was identified in the clockwise direction on the circular genome map which could potentially encode an 80-kDa polypeptide. Analysis of the predicted amino acid sequence of this ORF indicated that it was a homologue of the p87 capsid-associated gene of Orgyia pseudotsugata MNPV with an overall amino acid similarity of 34.3%. A late transcript of 2.1 kb was mapped to this open reading frame. An antisense 3.1-kb transcript partially overlapped the 5' end of the 2.1-kb RNA. Anti-extracellular virus sera reacted with a fusion protein consisting of a portion of the AcMNPV p80 gene fused to the bacterial trpE gene product, suggesting that the AcMNPV p80 gene product was also a component of the virus capsid.
对苜蓿银纹夜蛾核型多角体病毒67.2至68.5个图距单位的区域进行了测序。在环状基因组图谱上,从顺时针方向鉴定出一个大的开放阅读框(ORF),它可能编码一个80 kDa的多肽。对该ORF预测的氨基酸序列分析表明,它是云杉毒蛾核型多角体病毒p87衣壳相关基因的同源物,总体氨基酸相似性为34.3%。一个2.1 kb的晚期转录本被定位到这个开放阅读框。一个3.1 kb的反义转录本部分重叠2.1 kb RNA的5'端。抗细胞外病毒血清与一种融合蛋白发生反应,该融合蛋白由苜蓿银纹夜蛾核型多角体病毒p80基因的一部分与细菌trpE基因产物融合而成,这表明苜蓿银纹夜蛾核型多角体病毒p80基因产物也是病毒衣壳的一个组成部分。