Liu J C, Maruniak J E
Entomology and Nematology Department, University of Florida, Gainesville 32611-0620, USA.
J Gen Virol. 1995 Jun;76 ( Pt 6):1443-50. doi: 10.1099/0022-1317-76-6-1443.
The Spodoptera frugiperda multiple nucleocapsid nuclear polyhedrosis virus (SfMNPV) gp41 structural protein gene was located in the 1.9 kbp EcoRI-S fragment and sequenced. An open reading frame (ORF) of 999 nucleotides was detected that encoded a protein of 332 amino acids. The gp41 gene transcript was detected after 12 h post-infection (p.i.) and remained detectable at 48 h p.i. Two major mRNAs, about 1.6 and 2.8 kb in length, were determined by Northern blot analysis. Primer extension analysis demonstrated that the gp41 gene promoter region contains three transcription start sites. Two of the gp41 gene transcription start sites were located at -42 and -41 nucleotides from the ATG translation start codon within a consensus late transcription start site (TAAG) and another transcription start site was located at -140 nucleotides from the ATG translation start codon for which no consensus motif has been determined. Comparison of SfMNPV gp41 nucleotide and amino acid sequences with the gp41 genes from Autographa californica, Bombyx mori, and Helicoverpa zea NPVs showed 60% homology of nucleotide sequences and 70% similarity of amino acid sequences.
草地贪夜蛾多核衣壳核型多角体病毒(SfMNPV)的gp41结构蛋白基因位于1.9kbp的EcoRI - S片段中并进行了测序。检测到一个999个核苷酸的开放阅读框(ORF),其编码一个332个氨基酸的蛋白质。在感染后12小时(p.i.)检测到gp41基因转录本,并且在感染后48小时仍可检测到。通过Northern印迹分析确定了两个主要的mRNA,长度分别约为1.6kb和2.8kb。引物延伸分析表明,gp41基因启动子区域包含三个转录起始位点。其中两个gp41基因转录起始位点位于距ATG翻译起始密码子-42和-41个核苷酸处,处于一个共有晚期转录起始位点(TAAG)内,另一个转录起始位点位于距ATG翻译起始密码子-140个核苷酸处,尚未确定其共有基序。将SfMNPV gp41核苷酸和氨基酸序列与来自苜蓿银纹夜蛾、家蚕和玉米螟NPV的gp41基因进行比较,结果显示核苷酸序列同源性为60%,氨基酸序列相似性为70%。