Friesen P D, Miller L K
J Virol. 1987 Jul;61(7):2264-72. doi: 10.1128/JVI.61.7.2264-2272.1987.
The organization of viral genes within the 3.7-kilobase-pair HindIII-K/EcoRI-S region of the Autographa californica nuclear polyhedrosis virus genome (85 to 88 map units) was determined by using a combination of nucleotide sequencing, transcriptional mapping, and in vitro translation of hybrid selected RNA. Two nonoverlapping genes, extending in opposite directions and encoding polypeptides with molecular weights of 35,000 and 94,000 (35K and 94K polypeptides), were identified. Unspliced, messenger-active RNAs were transcribed from both genes early (2 h) after infection. Indicative of immediate-early genes, transcription of the divergent RNAs was unaffected by the protein synthesis inhibitor, cycloheximide. Late in infection, abundant RNAs were transcribed from promoters located at least 2.5 kilobase pairs upstream from the gene encoding the 35K polypeptide. These transcripts completely overlapped both the 35K and 94K polypeptide genes but apparently lacked protein-coding potential, suggesting that the transcripts may play a role in the suppression of early viral gene expression.
通过结合核苷酸测序、转录图谱分析以及杂交筛选RNA的体外翻译,确定了苜蓿银纹夜蛾核型多角体病毒基因组3.7千碱基对的HindIII-K/EcoRI-S区域(85至88个图谱单位)内病毒基因的组织方式。鉴定出两个不重叠的基因,它们向相反方向延伸,编码分子量分别为35,000和94,000的多肽(35K和94K多肽)。感染后早期(2小时),两个基因均转录出未剪接的、具有信使活性的RNA。作为立即早期基因的标志,这两种不同方向的RNA转录不受蛋白质合成抑制剂环己酰亚胺的影响。感染后期,大量RNA从位于编码35K多肽基因上游至少2.5千碱基对处的启动子转录而来。这些转录本完全重叠35K和94K多肽基因,但显然缺乏蛋白质编码潜力,这表明这些转录本可能在抑制早期病毒基因表达中发挥作用。