首页> 美国卫生研究院文献>Nucleic Acids Research >Role in translation of a triple tandemly repeated sequence in the 5-untranslated region of human thymidylate synthase mRNA.
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Role in translation of a triple tandemly repeated sequence in the 5-untranslated region of human thymidylate synthase mRNA.

机译:在人胸苷酸合酶mRNA 5-非翻译区的三重串联重复序列的翻译中的作用。

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摘要

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.
机译:在人胸苷酸合酶(TS)cDNA(pcHTS-1)中,ATG起始密码子的上游紧邻有一个由90个核苷酸组成的三级串联重复序列(TTR)。为了研究TTR在TS cDNA表达中的作用,我们使用pcHTS-1构建了突变的cDNA克隆,其中部分TTR被删除或插入了其他元件。将突变的cDNA质粒引入鼠TS-阴性突变细胞中,并通过测量TS活性的瞬时表达和转录的TS mRNA的量来确定突变cDNA的相对翻译效率。突变体瞬时表达中的翻译效率通过覆盖所有前两个重复元件以及最接近ATG起始密码子的第三个部分的缺失而增加,但是不受仅在前两个重复元件的一部分缺失的影响。 5'端。翻译效率也不受插入额外的重复元素到TTR中的影响。这些结果表明,在5'端的前两个重复元件都对TS mRNA的翻译具有抑制作用,这可能是由于该元件的独特结构特征。

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