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首页> 外文期刊>Insect Science >Analysis of a late gene, orf 101 from Helicoverpa armigera single nucleocapsid nucleopolyhedrovirus
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Analysis of a late gene, orf 101 from Helicoverpa armigera single nucleocapsid nucleopolyhedrovirus

机译:棉铃虫单核衣壳核多角体病毒的晚期基因orf 101的分析

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Helicoverpa armigera single nucleocapsid nucleopolyhedrovirus open reading frame 101 (ha101) is 762 nts in length and encodes a 254 amino acid peptide with predicted 29 kDa molecular weight. The homologues of ha101 were explored using BLASTP searching tool in the updated GenBank/EMBL and SWISS-PROT databases. The results showed that the homologues of ha101 were present in all the completely sequenced lepidopteran nucleopolyhedroviruses and granuloviruses, suggesting that ha101 might be a functional gene associated with their lepidopteran hosts. Sequence alignment of ha101 and its homologues revealed that 10 amino acids were completely conserved. RT-PCR analysis of ha101 manifested that the transcript of ha101 was first detected at 24 hpi and remained detectable at up to 122 hpi, suggesting that ha101 was transcribed during late stages of infection. Ha 101 was expressed using Bac to Bac system in Tn5B-1-4 cells. The product of ha101 expressed in Tn5B-1-4 cells was approximately 29 kDa, consistent with the predicted molecular weight, and the results were confirmed by western blot analysis. The subcellular localization indicated that ha101 was aggregated along nuclear envelope during the early stages of infection and spread out to the entire nucleus including virogenic stroma in late stages of infection, suggesting that ha101 may play a specific role in virion assembly process or virogenic stroma arrangement.
机译:棉铃虫单核衣壳核多角体病毒开放阅读框101(ha101)的长度为762 nt,编码一个254个氨基酸的肽,预测的分子量为29 kDa。在更新的GenBank / EMBL和SWISS-PROT数据库中使用BLASTP搜索工具探索了ha101的同源物。结果表明,在所有完全测序的鳞翅目核多角体病毒和颗粒病毒中均存在ha101的同源基因,这表明ha101可能是与其鳞翅目宿主相关的功能基因。 ha101及其同源物的序列比对揭示了10个氨基酸是完全保守的。 ha101的RT-PCR分析表明,ha101的转录本在24 hpi时首次被检测到,直到122 hpi仍可被检测到,这表明ha101在感染后期被转录。 Ha 101使用Bac to Bac系统在Tn5B-1-4细胞中表达。在Tn5B-1-4细胞中表达的ha101产物约为29 kDa,与预测的分子量相符,并且结果通过蛋白质印迹分析得到了证实。亚细胞定位表明,ha101在感染的早期沿核被膜聚集,并在感染的后期扩散到整个核,包括病毒源性基质,这表明ha101可能在病毒体组装过程或病毒源性基质排列中起特定作用。

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