Bicknell J N, Leisy D J, Rohrmann G F, Beaudreau G S
Department of Agricultural Chemistry, Oregon State University, Corvallis 97331.
Virology. 1987 Dec;161(2):589-92. doi: 10.1016/0042-6822(87)90155-3.
A 1.1-kb region of DNA containing the p26 gene of the multicapsid nuclear polyhedrosis virus of Orgyia pseudotsugata (OpMNPV) was sequenced, transcriptionally mapped, and compared to the same region in the MNPV of Autographa californica (AcMNPV). The mRNA start site of the p26 gene occurs about 22 nucleotides downstream from an A/T-rich putative promoter sequence that is highly conserved between AcMNPV and OpMNPV. The p26 mRNA is transcribed through the p26 gene and coterminates with the p10 gene resulting in a mRNA containing copies of both genes. The reading frames of the OpMNPV and AcMNPV p26 genes showed 47% amino acid sequence homology which is clustered in six regions with over 65% amino acid homology. There was a distinct bias toward incorporation of G/C-rich codons in the OpMNPV p26 gene. No DNA homology was observed between the region upstream of the p26 gene in AcMNPV and OpMNPV. In AcMNPV, this region contains the homologous repeated (hr) sequence hr5. Hybridization of a plasmid containing an AcMNPV-repeated sequence (hr5) to Southern blots of the OpMNPV genome indicated that this repeated sequence is lacking in OpMNPV.
对包含伪黄杉毒蛾多核衣壳核型多角体病毒(OpMNPV)p26基因的1.1千碱基对DNA区域进行了测序、转录图谱分析,并与苜蓿银纹夜蛾核型多角体病毒(AcMNPV)的相同区域进行了比较。p26基因的mRNA起始位点位于一个富含A/T的推定启动子序列下游约22个核苷酸处,该序列在AcMNPV和OpMNPV之间高度保守。p26 mRNA通过p26基因转录,并与p10基因共末端,产生一个包含两个基因拷贝的mRNA。OpMNPV和AcMNPV p26基因的阅读框显示出47%的氨基酸序列同源性,这些同源性集中在六个区域,氨基酸同源性超过65%。OpMNPV p26基因在富含G/C的密码子掺入方面存在明显偏向。在AcMNPV和OpMNPV的p26基因上游区域未观察到DNA同源性。在AcMNPV中,该区域包含同源重复(hr)序列hr5。一个含有AcMNPV重复序列(hr5)的质粒与OpMNPV基因组的Southern印迹杂交表明,OpMNPV中缺乏这个重复序列。