Mansour S L, Grodzicker T, Tjian R
Mol Cell Biol. 1986 Jul;6(7):2684-94. doi: 10.1128/mcb.6.7.2684-2694.1986.
We analyzed a set of adenovirus-simian virus 40 (SV40) hybrids in which the SV40 T antigen coding sequences are inserted downstream from the adenovirus major late promoter within the first, second, and third segments of the tripartite leader. In infected cells, these viruses give rise to a matched set of hybrid SV40 mRNAs that differ only in the number of tripartite leader segments attached to the complete SV40 T antigen coding region. We found that the number of tripartite leader segments present at the 5' end of the hybrid SV40 mRNAs had little effect on the efficiency of T antigen translation. Surprisingly, insertion of SV40 sequences within the first leader segment, at +33 relative to the start of transcription, significantly reduced the frequency of transcription initiation from the major late promoter. The 3' boundary of this downstream transcriptional control element was mapped between +33 and +190 by showing that insertion of SV40 sequences within the intron after the first leader segment at +190 had very little effect on transcription initiation from the late promoter. A transient expression assay was used to show that the effect of downstream sequences on transcription initiation from the major late promoter is dependent on a trans-acting factor encoded or induced by adenovirus.
我们分析了一组腺病毒 - 猴病毒40(SV40)杂种病毒,其中SV40 T抗原编码序列插入到腺病毒主要晚期启动子下游,位于三联前导序列的第一、第二和第三区段内。在受感染的细胞中,这些病毒产生了一组匹配的杂种SV40 mRNA,它们之间的差异仅在于与完整的SV40 T抗原编码区相连的三联前导序列区段的数量。我们发现,杂种SV40 mRNA 5'端存在的三联前导序列区段数量对T抗原的翻译效率影响很小。令人惊讶的是,在相对于转录起始点为 +33 的第一个前导序列区段内插入SV40序列,显著降低了主要晚期启动子的转录起始频率。通过显示在 +190 的第一个前导序列区段后的内含子内插入SV40序列对晚期启动子的转录起始影响很小,确定了这个下游转录控制元件的3'边界在 +33 和 +190 之间。使用瞬时表达分析表明,下游序列对主要晚期启动子转录起始的影响取决于腺病毒编码或诱导的一种反式作用因子。