Roseman N A, Hruby D E
J Virol. 1987 May;61(5):1398-406. doi: 10.1128/JVI.61.5.1398-1406.1987.
A vaccinia virus (VV) gene required for DNA replication has been mapped to the left side of the 16-kilobase (kb) VV HindIII D DNA fragment by marker rescue of a DNA- temperature-sensitive mutant, ts17, using cloned fragments of the viral genome. The region of VV DNA containing the ts17 locus (3.6 kb) was sequenced. This nucleotide sequence contains one complete open reading frame (ORF) and two incomplete ORFs reading from left to right. Analysis of this region at early times revealed that transcription from the incomplete upstream ORF terminates coincidentally with the complete ORF encoding the ts17 gene product, which is directly downstream. The predicted proteins encoded by this region correlate well with polypeptides mapped by in vitro translation of hybrid-selected early mRNA. The nucleotide sequences of a 1.3-kb BglII fragment derived from ts17 and from two ts17 revertants were also determined, and the nature of the ts17 mutation was identified. S1 nuclease protection studies were carried out to determine the 5' and 3' ends of the transcripts and to examine the kinetics of expression of the ts17 gene during viral infection. The ts17 transcript is present at both early and late times postinfection, indicating that this gene is constitutively expressed. Surprisingly, the transcriptional start throughout infection occurs at the proposed late regulatory element TAA, which immediately precedes the putative initiation codon ATG. Although the biological activity of the ts17-encoded polypeptide was not identified, it was noted that in ts17-infected cells, expression of a nonlinked VV immediate-early gene (thymidine kinase) was deregulated at the nonpermissive temperature. This result may indicate that the ts17 gene product is functionally required at an early step of the VV replicative cycle.
通过利用病毒基因组的克隆片段对DNA温度敏感突变体ts17进行标记拯救,已将痘苗病毒(VV)DNA复制所需的一个基因定位到16千碱基(kb)VV HindIII D DNA片段的左侧。对包含ts17基因座(3.6 kb)的VV DNA区域进行了测序。该核苷酸序列包含一个完整的开放阅读框(ORF)和两个从左到右的不完整ORF。对该区域早期的分析表明,来自上游不完整ORF的转录与编码ts17基因产物的完整ORF同时终止,该完整ORF就在其直接下游。该区域预测的蛋白质与通过杂交选择的早期mRNA体外翻译定位的多肽相关性良好。还确定了源自ts17和两个ts17回复株的1.3 kb BglII片段的核苷酸序列,并确定了ts17突变的性质。进行了S1核酸酶保护研究,以确定转录本的5'和3'末端,并检查病毒感染期间ts17基因的表达动力学。ts17转录本在感染后的早期和晚期均存在,表明该基因是组成型表达的。令人惊讶的是,整个感染过程中的转录起始发生在假定的晚期调控元件TAA处,该元件紧接在假定的起始密码子ATG之前。尽管未确定ts17编码多肽的生物学活性,但注意到在ts17感染的细胞中,未连锁的VV立即早期基因(胸苷激酶)的表达在非允许温度下失调。该结果可能表明ts17基因产物在VV复制周期的早期阶段在功能上是必需的。