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棉铃虫和小地老虎颗粒体病毒增强蛋白基因的特性分析

Characterization of the Helicoverpa armigera and Pseudaletia unipuncta granulovirus enhancin genes.

作者信息

Roelvink P W, Corsaro B G, Granados R R

机构信息

Boyce Thompson Institute for Plant Research, Cornell University, Ithaca, NY 14853, USA.

出版信息

J Gen Virol. 1995 Nov;76 ( Pt 11):2693-705. doi: 10.1099/0022-1317-76-11-2693.

DOI:10.1099/0022-1317-76-11-2693
PMID:7595376
Abstract

Enhancins are baculovirus proteins capable of enhancing infections in insect larvae by other baculoviruses. We have identified the enhancin proteins in four species of granulovirus (GV). In this paper we describe the cloning and sequencing of the enhancin genes of the Pseudaletia unipuncta granulovirus-Hawaiian strain (PsunGV-H) and the Helicoverpa (Heliothis) armigera granulovirus (HearGV). The PsunGV-H enhancin gene is virtually identical to the previously characterized Trichoplusia ni GV (TnGV) enhancin gene. In contrast, a comparison of the predicted amino acid sequences of TnGV enhancin (901 amino acids) and HearGV enhancin (902 amino acids) revealed an overall identity of only 80%, with greater conservation (88%) from amino acids 1-550. Primer extension analysis of enhancin RNAs identified the baculovirus late promoter motif that serves as the transcriptional start site in the HearGV enhancin gene. It is located three nucleotides from the putative enhancin translational initiator codon. RNase protection analysis demonstrated that both read-through and termination occur at the 3' end of the gene. Since a partial open reading frame (ORF) was identified immediately downstream of the 3' end of the enhancin ORF, these data suggested that a sizeable fraction of the enhancin mRNAs may be bi-cistronic and share a common 3' end with a downstream transcription unit.

摘要

增强蛋白是杆状病毒蛋白,能够增强其他杆状病毒对昆虫幼虫的感染。我们已在四种颗粒体病毒(GV)中鉴定出增强蛋白。在本文中,我们描述了伪夜蛾颗粒体病毒-夏威夷株(PsunGV-H)和棉铃虫颗粒体病毒(HearGV)增强蛋白基因的克隆和测序。PsunGV-H增强蛋白基因实际上与先前鉴定的粉纹夜蛾颗粒体病毒(TnGV)增强蛋白基因相同。相比之下,对TnGV增强蛋白(901个氨基酸)和HearGV增强蛋白(902个氨基酸)的预测氨基酸序列进行比较后发现,总体同一性仅为80%,在氨基酸1-550之间的保守性更高(88%)。对增强蛋白RNA进行引物延伸分析,确定了杆状病毒晚期启动子基序,该基序是HearGV增强蛋白基因的转录起始位点。它位于推测的增强蛋白翻译起始密码子的三个核苷酸处。核糖核酸酶保护分析表明,通读和终止均发生在该基因的3'端。由于在增强蛋白开放阅读框(ORF)的3'端下游立即鉴定出一个部分开放阅读框,这些数据表明,相当一部分增强蛋白mRNA可能是双顺反子的,并与下游转录单元共享一个共同的3'端。

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