Terui Yusuke, Higashi Kyohei, Tabei Yuzuru, Tomitori Hideyuki, Yamamoto Kaneyoshi, Ishihama Akira, Igarashi Kazuei, Kashiwagi Keiko
Faculty of Pharmacy, Chiba Institute of Science, Choshi, Chiba 288-0025, Japan.
J Bacteriol. 2009 Sep;191(17):5348-57. doi: 10.1128/JB.00387-09. Epub 2009 Jun 19.
Proteins whose synthesis is enhanced by polyamines at the level of translation were identified with a polyamine-requiring mutant cultured in the presence of 0.1% glucose and 0.02% glutamate at 42 degrees C. Polyamines had a greater effect on cell growth at 42 degrees C than at 37 degrees C. At 42 degrees C, the synthesis of RpoE (sigma(24)) and StpA, which are involved in the transcription of a number of heat shock response genes, was stimulated by polyamines at the level of translation. In the rpoE and stpA mRNAs, a Shine-Dalgarno (SD) sequence is located at 13 and 12 nucleotides, respectively, upstream of the initiation codon AUG. When the SD sequences were moved to the more common position 7 nucleotides upstream of the initiation codon AUG, the degree of polyamine stimulation was reduced, although the level of RpoE and StpA synthesis was markedly increased. The mechanism underlying polyamine stimulation of RpoE synthesis was then studied. Polyamine stimulation of RpoE synthesis was reduced by changing the bulged-out structure in the initiation site of rpoE mRNA, although the level of RpoE synthesis increased. A selective structural change of this bulged-out region induced by spermidine at 42 degrees C was observed by circular dichroism. Polyamine stimulation of fMet-tRNA binding to ribosomes at 42 degrees C also disappeared by changing the bulged-out structure in the initiation site of rpoE mRNA. The results suggest that polyamines enhance the synthesis of RpoE by changing the bulged-out structure in the initiation site of rpoE mRNA.
通过在42℃下于含0.1%葡萄糖和0.02%谷氨酸的培养基中培养多胺需求型突变体,鉴定出在翻译水平上多胺增强其合成的蛋白质。多胺在42℃时对细胞生长的影响大于在37℃时。在42℃时,参与多个热休克反应基因转录的RpoE(σ24)和StpA的合成在翻译水平上受到多胺的刺激。在rpoE和stpA mRNA中,Shine-Dalgarno(SD)序列分别位于起始密码子AUG上游13和12个核苷酸处。当SD序列移至起始密码子AUG上游更常见的7个核苷酸位置时,尽管RpoE和StpA的合成水平显著增加,但多胺刺激程度降低。随后研究了多胺刺激RpoE合成的机制。通过改变rpoE mRNA起始位点的突出结构,多胺对RpoE合成的刺激作用降低,尽管RpoE的合成水平有所增加。通过圆二色性观察到在42℃时亚精胺诱导该突出区域发生选择性结构变化。通过改变rpoE mRNA起始位点的突出结构,在42℃时多胺对fMet-tRNA与核糖体结合的刺激作用也消失了。结果表明,多胺通过改变rpoE mRNA起始位点的突出结构来增强RpoE的合成。