Vega Laso M R, Zhu D, Sagliocco F, Brown A J, Tuite M F, McCarthy J E
Department of Gene Expression, GBF-Gesellschaft für Biotechnologische Forschung mbH, Braunschweig, Federal Republic of Germany.
J Biol Chem. 1993 Mar 25;268(9):6453-62.
A new modular in vivo/in vitro expression system was constructed which facilitates studies of the control and regulation of gene expression in the yeast Saccharomyces cerevisiae. We studied the influence of stem-loop structures inserted into the non-translated leader region upon the steady-state levels and translation of mRNAs bearing the cat gene from the bacterial transposon Tn9. mRNA abundance changed relatively little in response to alterations in the leader sequence and structure, whereas stem-loop structures clearly inhibited translation to a degree that was dependent upon the predicted stability as well as the position of the inserted secondary structure. A stem-loop structure with a predicted stability greater than -28 kcal mol-1 and with a stem comprising at least 15 (mainly G/C) base pairs inhibited translation in vivo by at least 98%. A stem-loop structure with a predicted stability of approximately -14 kcal mol-1, whose stem comprised at least six G/C base pairs, inhibited translation in vivo by at least 66%. The hairpins were more inhibitory when placed close to the start codon than when positioned near the 5' end of the leader. An mRNA showing extensive complementarity between the leader and trailer regions was not only poorly translated but also had a steady-state level at least three times higher than the average for all the cat constructs examined. Translation of the various mRNAs in a yeast cell-free system followed qualitatively the same pattern as the results obtained in vivo. The stem-loop structures were far less inhibitory in a reticulocyte lysate system. Overall, the data are likely to reflect the full spectrum of translational activities of yeast mRNAs in vivo determined by secondary structure and emphasize the importance of translation as a control step in gene expression.
构建了一种新的模块化体内/体外表达系统,该系统有助于研究酿酒酵母中基因表达的控制和调节。我们研究了插入非翻译前导区的茎环结构对携带来自细菌转座子Tn9的cat基因的mRNA的稳态水平和翻译的影响。mRNA丰度对前导序列和结构的改变反应相对较小,而茎环结构明显抑制翻译,其抑制程度取决于预测的稳定性以及插入的二级结构的位置。预测稳定性大于-28 kcal/mol且茎至少包含15个(主要是G/C)碱基对的茎环结构在体内至少抑制98%的翻译。预测稳定性约为-14 kcal/mol且茎至少包含6个G/C碱基对的茎环结构在体内至少抑制66%的翻译。发夹结构靠近起始密码子放置时比靠近前导区5'端放置时抑制作用更强。一种在前导区和尾随区之间显示出广泛互补性的mRNA不仅翻译效率低,而且其稳态水平比所有检测的cat构建体的平均水平至少高三倍。酵母无细胞系统中各种mRNA的翻译在定性上与体内获得的结果遵循相同的模式。在网织红细胞裂解物系统中,茎环结构的抑制作用要小得多。总体而言,这些数据可能反映了由二级结构决定的酵母mRNA在体内翻译活性的全貌,并强调了翻译作为基因表达控制步骤的重要性。