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Preferential translation of cold-shock mRNAs during cold adaptation

机译:冷适应过程中冷休克mRNA的优先翻译

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Upon temperature downshift below the lower threshold of balanced growth (similar to20degreesC), the Escherichia coli translational apparatus undergoes modifications allowing the selective translation of the transcripts of cold shock-induced genes, while bulk protein synthesis is drastically reduced. Here we were able to reproduce this translational bias in E. coli cell-free extracts prepared at various times during cold adaptation which were found to display different capacities to translate different types of mRNAs as a function of temperature. Several causes were found to contribute to the cold-shock translational bias: Cold-shock mRNAs contain cis-elements, making them intrinsically more prone to being translated in the cold, and they are selective targets for trans-acting factors present in increased amounts in the translational apparatus of cold-shocked cells. CspA was found to be among these trans-acting factors. In addition to inducing a higher level of CspA, cold shock was found to cause a strong (two-to threefold) stoichiometric imbalance of the ratio between initiation factors (IF1, IF2, IF3) and ribosomes without altering the stoichiometric ratio between the factors themselves. The most important sources of cold-shock translational bias is IF3, which strongly and selectively favors translation of cold-shock mRNAs in the cold. IF1 and the RNA chaperone CspA, which stimulate translation preferentially in the cold without mRNA selectivity, can also contribute to the translational bias. Finally, in contrast to a previous claim, translation of cold-shock cspA mRNA in the cold was found to be as sensitive as that of a non-cold-shock mRNA to both chloramphenicol and kanamycin inhibition. [References: 24]
机译:当温度下降到低于平衡生长的下限阈值(类似于20摄氏度)时,大肠杆菌翻译设备会进行修饰,从而允许冷休克诱导基因的转录本选择性翻译,而大量蛋白质的合成则大大减少。在这里,我们能够在冷适应期间的不同时间制备的大肠杆菌无细胞提取物中复制这种翻译偏倚,发现该提取物显示出随温度变化而翻译不同类型的mRNA的不同能力。已发现造成冷休克翻译偏倚的多种原因:冷休克mRNA含有顺式元件,使它们本质上更容易在寒冷中被翻译,并且它们是反式作用因子的选择性靶标,而反式作用因子的存在量增加。冷休克细胞的翻译装置。发现CspA在这些反式作用因子中。除了诱导更高水平的CspA外,还发现冷休克会引起起始因子(IF1,IF2,IF3)和核糖体之间的比率存在强烈的(两到三倍)化学计量失衡,而不会改变这些因素本身之间的化学计量比率。冷休克翻译偏倚的最重要来源是IF3,IF3强烈且选择性地有利于冷休克mRNA的翻译。 IF1和RNA伴侣CspA在寒冷中优先刺激翻译而无mRNA选择性,也可能导致翻译偏倚。最后,与先前的权利要求相反,发现冷休克cspA mRNA的翻译与非冷休克mRNA的氯霉素和卡那霉素抑制作用一样敏感。 [参考:24]

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