Olsson C L, Graffe M, Springer M, Hershey J W
Department of Biological Chemistry, School of Medicine, University of California, Davis 95616, USA.
Mol Gen Genet. 1996 Apr 10;250(6):705-14. doi: 10.1007/BF02172982.
To investigate the physiological roles of translation initiation factor IF3 and ribosomal protein L20 in Escherichia coli, the infC, rpmI and rpIT genes encoding IF3, L35 and L20, respectively, were placed under the control of lac promotor/operator sequences. Thus, their expression is dependent upon the amount of inducer isopropyl thiogalactoside (IPTG) in the medium. Lysogenic strains were constructed with recombinant lambda phages that express either rpmI and rplT or infC and prmI in trans, thereby allowing depletion of only IF3 or L20 at low IPTG concentrations. At low cellular concentration of IF3, but not L20, decreases and the growth rate slows. Furthermore, ribosomes run off polysomes, indicating that IF3 functions during the initiation phase of protein synthesis in vivo. During slow growth, the ratio of RNA to protein increases rather than decreases as occurs with control strains, indicating that IF3 limitation disrupts feedback inhibition of rRNA synthesis. As IF3 levels drop, expression from an AUU-infC-lacZ fusion increases, whereas expression decreases from an AUG-infC-lacZ fusion, thereby confirming the model of autogenous regulation of infC. The effects of L20 limitation are similar; cells grown in low concentrations of IPTG exhibited a decrease in the rate of growth, a decrease in cellular L20 concentration, no change in IF3 concentration, and a small increase in the ratio of RNA to protein. In addition, a decrease in 50S subunits and the appearance of an aberrant ribosome peak at approximately 41-43S is seen. Previous studies have shown that the L20 protein negatively controls its own gene expression. Reduction of the cellular concentration of L20 derepresses the expression of an rplT-lacZ gene fusion, thus confirming autogenous regulation by L20.
为了研究翻译起始因子IF3和核糖体蛋白L20在大肠杆菌中的生理作用,分别编码IF3、L35和L20的infC、rpmI和rpIT基因被置于乳糖启动子/操纵序列的控制之下。因此,它们的表达取决于培养基中诱导剂异丙基硫代半乳糖苷(IPTG)的量。用重组λ噬菌体构建溶原性菌株,这些噬菌体反式表达rpmI和rplT或infC和prmI,从而在低IPTG浓度下仅使IF3或L20耗尽。在IF3细胞浓度低时,但不是L20,细胞数量减少且生长速率减慢。此外,核糖体从多聚核糖体上脱离,表明IF3在体内蛋白质合成的起始阶段发挥作用。在缓慢生长期间,RNA与蛋白质的比率增加而不是像对照菌株那样减少,这表明IF3的限制破坏了rRNA合成的反馈抑制。随着IF3水平下降,AUU-infC-lacZ融合体的表达增加,而AUG-infC-lacZ融合体的表达减少,从而证实了infC的自体调节模型。L20限制的影响类似;在低浓度IPTG中生长的细胞生长速率降低,细胞L20浓度降低,IF3浓度不变,RNA与蛋白质的比率略有增加。此外,观察到50S亚基减少以及在约41 - 43S处出现异常核糖体峰。先前的研究表明,L20蛋白对其自身的基因表达具有负调控作用。细胞L20浓度的降低会解除rplT-lacZ基因融合体的表达抑制,从而证实L20的自体调节作用。