Kashiwagi K, Watanabe R, Igarashi K
Faculty of Pharmaceutical Sciences, Chiba University, Japan.
Biochem Biophys Res Commun. 1994 Apr 15;200(1):591-7. doi: 10.1006/bbrc.1994.1489.
Since the speF-potE operon (pPT71 clone) encoding inducible ornithine decarboxylase (iODC) and polyamine transport potE protein is inducible at acidic pH, a gene encoding a protein involved in the enhancement of expression of the operon was searched for. Using the fused gene containing the upstream sequence of the speF-potE operon and the open reading frame of beta-galactosidase as a reporter gene, a clone (pPTS23) which causes the increase of beta-galactosidase activity at acidic pH was isolated. The clone also increased iODC activity at acidic pH and was identified as a gene encoding RNase III. This is the first example that RNase III increases the translational efficiency of mRNA derived from Escherichia coli gene by cutting the 5'-untranslated region of mRNA.
由于编码诱导型鸟氨酸脱羧酶(iODC)和多胺转运蛋白potE的speF-potE操纵子(pPT71克隆)在酸性pH下可诱导,因此寻找了一个编码参与该操纵子表达增强的蛋白质的基因。使用包含speF-potE操纵子上游序列和β-半乳糖苷酶开放阅读框的融合基因作为报告基因,分离出一个在酸性pH下导致β-半乳糖苷酶活性增加的克隆(pPTS23)。该克隆在酸性pH下也增加了iODC活性,并被鉴定为编码RNase III的基因。这是RNase III通过切割mRNA的5'-非翻译区来提高源自大肠杆菌基因的mRNA翻译效率的首个实例。