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云杉芽卷叶蛾多粒包埋核型多角体病毒主要结构蛋白p39编码基因的核苷酸序列、转录图谱及时间表达

Nucleotide sequence, transcriptional mapping, and temporal expression of the gene encoding p39, a major structural protein of the multicapsid nuclear polyhedrosis virus of Orgyia pseudotsugata.

作者信息

Blissard G W, Quant-Russell R L, Rohrmann G F, Beaudreau G S

机构信息

Department of Agricultural Chemistry, Oregon State University, Corvallis 97331-6502.

出版信息

Virology. 1989 Feb;168(2):354-62. doi: 10.1016/0042-6822(89)90276-6.

DOI:10.1016/0042-6822(89)90276-6
PMID:2644736
Abstract

The gene encoding the 39-kDa major structural protein (p39) of Orgyia pseudotsugata nuclear polyhedrosis virus (OpMNPV) was sequenced and transcriptionally mapped, and its expression was examined at various times postinfection. By Northern hybridization, primer extension, and S1 nuclease analysis, we identified p39 mRNAs of approximately 2600 nt. By primer extension analysis, we identified two major sets of transcripts which initiated around -48 and -96 nt upstream of the translation start codon. The transcription start sites were located within the conserved baculovirus late gene consensus sequence, ATAAG, which is duplicated in the p39 5' flanking region. In OpMNPV-infected Lymantria dispar cells, the p39 mRNAs were expressed abundantly at 24 and 36 hr p.i. but were present in lower quantities at 48 hr p.i. The p39 gene contained an open reading frame of 1053 nt which encodes a predicted protein of 351 amino acids with an estimated molecular weight of 39.5 kDa. Three repeats of the amino acid sequence Ala-Pro-Ala-Ala-Pro were identified at the C-terminus of the predicted p39 protein.

摘要

对云杉芽卷叶蛾核型多角体病毒(OpMNPV)编码39 kDa主要结构蛋白(p39)的基因进行了测序和转录图谱分析,并检测了其在感染后不同时间的表达情况。通过Northern杂交、引物延伸和S1核酸酶分析,我们鉴定出约2600 nt的p39 mRNA。通过引物延伸分析,我们鉴定出两组主要转录本,它们在翻译起始密码子上游约-48和-96 nt处起始。转录起始位点位于保守的杆状病毒晚期基因共有序列ATAAG内,该序列在p39 5'侧翼区域重复。在OpMNPV感染的舞毒蛾细胞中,p39 mRNA在感染后24和36小时大量表达,但在感染后48小时表达量较低。p39基因包含一个1053 nt的开放阅读框,编码一个预测的351个氨基酸的蛋白质,估计分子量为39.5 kDa。在预测的p39蛋白的C末端鉴定出氨基酸序列Ala-Pro-Ala-Ala-Pro的三个重复序列。

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