Wu J G, Miller L K
Department of Entomology, University of Georgia, Athens 30602.
J Gen Virol. 1989 Sep;70 ( Pt 9):2449-59. doi: 10.1099/0022-1317-70-9-2449.
A 1.4 kb region downstream of the DNA polymerase gene of Autographa californica nuclear polyhedrosis virus was sequenced. Two open reading frames (ORFs) were identified of 927 and 474 bases in length. The 927 base ORF encodes a 34.8K protein as determined by in vitro translation of both hybrid-selected RNA and RNA synthesized in vitro from a 927 base ORF template. The predicted amino acid sequence of the 34.8K polypeptide (p34.8) reveals a hydrophobic N terminus, two potential N-glycosylation sites, and potential sites for phosphorylation by casein kinase I and protein kinase C. The p34.8 gene has a strong codon usage bias which is strikingly different from that of the polyhedrin gene. The two 5' ends of the 927 base ORF transcripts initiate from an ATAAG sequence and a GTAAG sequence 11 and 87 bases upstream of the ATG codon respectively. A short upstream reading frame is present in the leader sequence of the longer RNA. The transcripts have multiple 3' ends; the most proximal endpoint correlates with a polyadenylation signal overlapping the translational termination codon of the 927 base ORF. Transcripts of the latter were not observed early in the infection cycle but appeared 6 h after infection and were maximally expressed at 12 to 24 h post-infection. The late nature of these transcripts was confirmed by their sensitivity to aphidicolin and cycloheximide, inhibitors of DNA replication and protein synthesis respectively. Attempts to construct viral mutants carrying a deletion of the p34.8 gene and fusion with the beta-galactosidase gene suggest that the former gene is essential for viral replication.
对苜蓿银纹夜蛾核型多角体病毒DNA聚合酶基因下游的一个1.4kb区域进行了测序。鉴定出两个开放阅读框(ORF),长度分别为927和474个碱基。通过对杂交选择的RNA以及从927碱基ORF模板体外合成的RNA进行体外翻译,确定927碱基的ORF编码一种34.8K的蛋白质。预测的34.8K多肽(p34.8)的氨基酸序列显示出一个疏水的N末端、两个潜在的N-糖基化位点以及酪蛋白激酶I和蛋白激酶C的潜在磷酸化位点。p34.8基因具有很强的密码子使用偏好性,这与多角体蛋白基因的密码子使用偏好性显著不同。927碱基ORF转录本的两个5'端分别从ATG密码子上游11和87个碱基处的ATAAG序列和GTAAG序列起始。在较长RNA的前导序列中存在一个短的上游阅读框。转录本有多个3'端;最靠近的终点与一个多聚腺苷酸化信号相关,该信号与927碱基ORF的翻译终止密码子重叠。在感染周期早期未观察到后者的转录本,但在感染后6小时出现,并在感染后12至24小时达到最大表达。这些转录本的晚期性质通过它们对阿非迪霉素和放线菌酮(分别为DNA复制和蛋白质合成的抑制剂)的敏感性得到证实。构建携带p34.8基因缺失并与β-半乳糖苷酶基因融合的病毒突变体的尝试表明,前一个基因对于病毒复制是必不可少的。