Rosel J L, Earl P L, Weir J P, Moss B
J Virol. 1986 Nov;60(2):436-49. doi: 10.1128/JVI.60.2.436-449.1986.
The sequence of the 8,600-base-pair HindIII H fragment, located at the center of the vaccinia virus genome, was determined to analyze several late genes. Seven major complete open reading frames (ORFs) and two that started from or continued into adjacent DNA segments were identified. ORFs were closely spaced and present on both DNA strands. Some adjacent ORFs had oppositely oriented overlapping termination codons or contiguous stop and start codons. Nucleotide compositional analysis indicated that the A-T frequency was consistently lowest in the first codon position. The sizes of the polypeptides predicted from the DNA sequence were compared with those determined by polyacrylamide gel electrophoresis of cell-free translation products of mRNAs selected by hybridization to cloned single-stranded DNA segments or synthesized in vitro by bacteriophage T7 RNA polymerase. Six transcripts that initiated within the HindIII H DNA fragment were detected, and of these, four were synthesized only at late times, one was synthesized only early, and one was synthesized early and late. The sites on the genome corresponding to the 5' ends of the transcripts were located by high-resolution nuclease S1 analysis. For late genes, the transcriptional and translational initiation sites mapped within a few nucleotides of each other, and in each case the sequence TAAATGG occurred at the start of the ORF. The extremely short leader and the absence of A or G in the -3 position, relative to the first nucleotide of the initiation codon, distinguishes the majority of vaccinia virus late genes from eucaryotic and vaccinia virus early genes.
位于痘苗病毒基因组中心的8600个碱基对的HindIII H片段的序列被测定,以分析几个晚期基因。鉴定出七个主要的完整开放阅读框(ORF)以及两个起始于或延伸至相邻DNA片段的开放阅读框。开放阅读框间隔紧密,存在于两条DNA链上。一些相邻的开放阅读框具有相反方向的重叠终止密码子或相邻的终止和起始密码子。核苷酸组成分析表明,A-T频率在第一个密码子位置始终最低。将根据DNA序列预测的多肽大小与通过与克隆的单链DNA片段杂交选择的mRNA的无细胞翻译产物或由噬菌体T7 RNA聚合酶体外合成的产物进行聚丙烯酰胺凝胶电泳测定的大小进行比较。检测到六个在HindIII H DNA片段内起始的转录本,其中四个仅在晚期合成,一个仅在早期合成,一个在早期和晚期都合成。通过高分辨率核酸酶S1分析确定了基因组上与转录本5'端相对应的位点。对于晚期基因,转录起始位点和翻译起始位点在彼此几个核苷酸的范围内定位,并且在每种情况下,序列TAAATGG出现在开放阅读框的起始处。相对于起始密码子的第一个核苷酸,-3位置的极短前导序列以及A或G的缺失将大多数痘苗病毒晚期基因与真核生物和痘苗病毒早期基因区分开来。