Laboratory of Genetics, Department of Biosciences and Biotechnology University of Camerino, 62032 Camerino (MC), Italy.
Nucleic Acids Res. 2019 May 21;47(9):4638-4651. doi: 10.1093/nar/gkz187.
After a 37 to 10°C temperature downshift the level of translation initiation factor IF2, like that of IF1 and IF3, increases at least 3-fold with respect to the ribosomes. To clarify the mechanisms and conditions leading to cold-stress induction of infB expression, the consequences of this temperature shift on infB (IF2) transcription, infB mRNA stability and translation were analysed. The Escherichia coli gene encoding IF2 is part of the metY-nusA-infB operon that contains three known promoters (P-1, P0 and P2) in addition to two promoters P3 and P4 identified in this study, the latter committed to the synthesis of a monocistronic mRNA encoding exclusively IF2. The results obtained indicate that the increased level of IF2 following cold stress depends on three mechanisms: (i) activation of all the promoters of the operon, P-1 being the most cold-responsive, as a likely consequence of the reduction of the ppGpp level that follows cold stress; (ii) a large increase in infB mRNA half-life and (iii) the cold-shock induced translational bias that ensures efficient translation of infB mRNA by the translational apparatus of cold shocked cells. A comparison of the mechanisms responsible for the cold shock induction of the three initiation factors is also presented.
在 37 到 10°C 的温度骤降之后,起始因子 IF2 的翻译水平至少增加了 3 倍,相对于核糖体而言。为了阐明导致冷应激诱导 infB 表达的机制和条件,分析了这种温度变化对 infB(IF2)转录、infB mRNA 稳定性和翻译的影响。编码 IF2 的大肠杆菌基因是 metY-nusA-infB 操纵子的一部分,该操纵子除了本研究中鉴定的两个启动子 P3 和 P4 外,还包含三个已知的启动子(P-1、P0 和 P2),后者负责合成仅编码 IF2 的单顺反子 mRNA。结果表明,冷应激后 IF2 水平的增加取决于三种机制:(i)操纵子所有启动子的激活,P-1 是最冷响应的,可能是由于冷应激后 ppGpp 水平降低所致;(ii)infB mRNA 半衰期的大幅增加;(iii)冷休克诱导的翻译偏差,通过冷休克细胞的翻译装置确保 infB mRNA 的有效翻译。还比较了导致三种起始因子冷休克诱导的机制。