Kimura Akiko, Ohashi Kazuaki, Naganuma Akira
Laboratory of Molecular and Biochemical Toxicology, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.
J Cell Physiol. 2007 Feb;210(2):378-84. doi: 10.1002/jcp.20845.
The response of Saccharomyces cerevisiae to cisplatin was investigated by examining variations in gene expression using cDNA microarrays and confirming the results by reverse transcription polymerase chain reaction (RT-PCR). The mRNA levels of 14 proteins involved in iron homeostasis were shown to be increased by cisplatin. Interestingly, the expression of all 14 genes is known to be regulated by Aft1, a transcription factor activated in response to iron insufficiency. The promoter of one of these genes, FET3, has been relatively well studied, so we performed a reporter assay using the FET3 promoter and showed that an Aft1 binding site in the promoter region is indispensable for induction of transcription by cisplatin. The active domain of Aft1 necessary for activation of the FET3 promoter by cisplatin is identical to the one required for activation by bathophenanthroline sulfonate, an inhibitor of cellular iron uptake. Furthermore, we found that cisplatin inhibits the uptake of (55)Fe(II) into yeast cells. These findings suggest that cisplatin activates Aft1 through the inhibition of iron uptake into the cells, after which the expression of Aft1 target genes involved in iron uptake might be induced.
通过使用cDNA微阵列检测基因表达变化并通过逆转录聚合酶链反应(RT-PCR)确认结果,研究了酿酒酵母对顺铂的反应。结果显示,顺铂可使14种参与铁稳态的蛋白质的mRNA水平升高。有趣的是,已知所有这14个基因的表达均受Aft1调控,Aft1是一种在铁缺乏时被激活的转录因子。其中一个基因FET3的启动子已得到较为充分的研究,因此我们使用FET3启动子进行了报告基因检测,结果表明启动子区域中的Aft1结合位点对于顺铂诱导转录是必不可少的。顺铂激活FET3启动子所需的Aft1活性结构域与邻菲罗啉磺酸盐(一种细胞铁摄取抑制剂)激活所需的结构域相同。此外,我们发现顺铂会抑制(55)Fe(II)进入酵母细胞。这些发现表明,顺铂通过抑制细胞对铁的摄取来激活Aft1,此后可能会诱导参与铁摄取的Aft1靶基因的表达。