Woo Soo-Dong, Choi Jae Young, Je Yeon Ho, Jin Byung Rae
Department of Plant Medicine, College of Agriculture, Life and Environment Sciences, Chungbuk National University, Cheongju 361-763, Korea.
J Biosci. 2006 Sep;31(3):329-38. doi: 10.1007/BF02704105.
A local strain of Helicoverpa assulta nucleopolyhedrovirus (HasNPV) was isolated from infected H.assulta larvae in Korea. Restriction endonuclease fragment analysis, using 4 restriction enzymes, estimated that the total genome size of HasNPV is about 138 kb. A degenerate polymerase chain reaction (PCR) primer set for the polyhedrin gene successfully amplified the partial polyhedrin gene of HasNPV. The sequencing results showed that the about 430 bp PCR product was a fragment of the corresponding polyhedrin gene. Using HasNPV partial predicted polyhedrin to probe the Southern blots, we identified the location of the polyhedrin gene within the 6 kb Eco RI, 15 kb Nco I, 20 kb Xho I, 17 kb Bgl II and 3 kb Cla I fragments, respectively. The 3 kb Cla I fragment was cloned and the nucleotide sequences of the polyhedrin coding region and its flaking regions were determined. Nucleotide sequence analysis indicated the presence of an open reading frame of 735 nucleotides which could encode 245 amino acids with a predicted molecular mass of 29 kDa. The nucleotide sequences within the coding region of HasNPV polyhedrin shared 73.7% identity with the polyhedrin gene from Autographa californica NPV but were most closely related to Helicoverpa and Heliothis species NPVs with over 99% sequence identity.
从韩国感染的烟青虫幼虫中分离出了一株本地烟青虫核型多角体病毒(HasNPV)。使用4种限制性内切酶进行的限制性内切酶片段分析估计,HasNPV的总基因组大小约为138 kb。一组用于多角体蛋白基因的简并聚合酶链反应(PCR)引物成功扩增出了HasNPV的部分多角体蛋白基因。测序结果表明,约430 bp的PCR产物是相应多角体蛋白基因的一个片段。用HasNPV部分预测的多角体蛋白探测Southern杂交印迹,我们分别在6 kb的Eco RI、15 kb的Nco I、20 kb的Xho I、17 kb的Bgl II和3 kb的Cla I片段中确定了多角体蛋白基因的位置。克隆了3 kb的Cla I片段,并测定了多角体蛋白编码区及其侧翼区的核苷酸序列。核苷酸序列分析表明存在一个735个核苷酸的开放阅读框,它可以编码245个氨基酸,预测分子量为29 kDa。HasNPV多角体蛋白编码区内的核苷酸序列与苜蓿银纹夜蛾核型多角体病毒的多角体蛋白基因有73.7%的同源性,但与烟青虫和棉铃虫属物种的核型多角体病毒关系最为密切,序列同源性超过99%。