Kaneda S, Takeishi K, Ayusawa D, Shimizu K, Seno T, Altman S
Nucleic Acids Res. 1987 Feb 11;15(3):1259-70. doi: 10.1093/nar/15.3.1259.
A triple tandem repeat (TTR) consisting of 90 nucleotides exists immediately upstream of the ATG initiator codon in human thymidylate synthase (TS) cDNA (pcHTS-1). To investigate the role of the TTR in the expression of the TS cDNA, we used pcHTS-1 to construct mutant cDNA clones in which part of the TTR was deleted or an additional element was inserted. The mutant cDNA plasmid was introduced into murine TS-negative mutant cells and the relative translation efficiencies of the mutant cDNAs were determined by measuring the transient expression of TS activity and the amount of TS mRNA transcribed. The translation efficiency in transient expression of the mutants was increased by deletions covering all the first two repeated elements, and the part of the third closest to the ATG initiator codon, but was not affected by deletions of only parts of the first two repeated elements at the 5' end. The translation efficiency was also not affected by insertion of an additional repeated element into the TTR. These results suggest that the first two repeated elements at the 5' end both have inhibitory effects on translation of the TS mRNA, probably due to the unique structural feature of this element.
在人胸苷酸合成酶(TS)cDNA(pcHTS - 1)中,一个由90个核苷酸组成的三联串联重复序列(TTR)存在于ATG起始密码子的紧邻上游。为了研究TTR在TS cDNA表达中的作用,我们使用pcHTS - 1构建了突变cDNA克隆,其中部分TTR被删除或插入了一个额外的元件。将突变cDNA质粒导入鼠TS阴性突变细胞,并通过测量TS活性的瞬时表达和转录的TS mRNA量来确定突变cDNA的相对翻译效率。覆盖前两个重复元件全部以及最靠近ATG起始密码子的第三个重复元件部分的缺失会提高突变体瞬时表达中的翻译效率,但仅5'端前两个重复元件部分的缺失对其没有影响。向TTR中插入一个额外的重复元件也不会影响翻译效率。这些结果表明,5'端的前两个重复元件对TS mRNA的翻译均具有抑制作用,这可能归因于该元件独特的结构特征。