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埃及棉铃虫核型多角体病毒B型lef-3基因的鉴定与特性分析

Identification and characterization of the Spodoptera littoralis nucleopolyhedrovirus type B lef-3 gene.

作者信息

Wolff J L, Herzog L M, Sun L, Levin D B

机构信息

Department of Biology, University of Victoria, Canada.

出版信息

Arch Virol. 1998;143(4):743-67. doi: 10.1007/s007050050327.

DOI:10.1007/s007050050327
PMID:9638145
Abstract

We have identified a gene from the Spodoptera littoralis nucleopolyhedrovirus type B (SpliNPV-B) with several characteristics that suggest that it is homologous to the lef-3 genes of the Autographa californica and Orgyia pseudotsugata NPVs (AcMNPV and OpMNPV, respectively). The SpliNPV-B lef-3 gene was mapped between 43.6 and 45.5 map units of the SpliNPV-B genome. Northern blot analysis showed that SpliNPV-B lef-3 was expressed as a 1.6 Kb transcript at 5 h post infection (p.i.), reached high levels at 24 h p.i., and remained highly expressed at 56 h p.i. Transcription of SpliNPV-B lef-3 initiated at two distinct sites downstream from a TATA-box motif and terminated 25 nucleotides downstream from the translation stop site of the putative LEF-3 polypeptide. The 5'-boundaries of lef-3 promoter elements were investigated by transient expression assays, which revealed that the major components of the lef-3 promoter are within a 183 base pair region upstream of the distal transcription initiation site. Transfection of SpliNPV-B infected Sf9 cells with anti-sense oligonucleotides designed to inhibit LEF-3 expression resulted in substantial reduction of viral DNA replication, suggesting that the role of SpliNPV-B lef-3 may be similar to that of AcMNPV and OpMNPV lef-3 genes, which are essential for viral DNA replication.

摘要

我们从滨海灰翅夜蛾核型多角体病毒B型(SpliNPV - B)中鉴定出一个基因,该基因具有若干特征,表明它与苜蓿银纹夜蛾核型多角体病毒(AcMNPV)和云杉毒蛾核型多角体病毒(OpMNPV)的lef - 3基因同源。SpliNPV - B lef - 3基因定位于SpliNPV - B基因组的43.6至45.5个图谱单位之间。Northern印迹分析表明,SpliNPV - B lef - 3在感染后5小时(p.i.)表达为1.6 Kb的转录本,在感染后24小时达到高水平,并在感染后56小时保持高表达。SpliNPV - B lef - 3的转录起始于TATA框基序下游的两个不同位点,并在假定的LEF - 3多肽翻译终止位点下游25个核苷酸处终止。通过瞬时表达分析研究了lef - 3启动子元件的5'边界,结果表明lef - 3启动子的主要成分位于远端转录起始位点上游183个碱基对区域内。用设计用于抑制LEF - 3表达的反义寡核苷酸转染SpliNPV - B感染的Sf9细胞,导致病毒DNA复制大幅减少,这表明SpliNPV - B lef - 3的作用可能与AcMNPV和OpMNPV lef - 3基因相似,它们对病毒DNA复制至关重要。

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