Kimura Akiko, Ohashi Kazuaki, Yamamoto Reiko, Naganuma Akira
Laboratory of Molecular and Biochemical Toxicology, Graduate School of Pharmaceutical Sciences, Tohoku University, Aoba-ku, Sendai 980-8578, Japan.
J Toxicol Sci. 2006 Aug;31(3):287-90. doi: 10.2131/jts.31.287.
cDNA microarray analysis indicated that mRNA levels of Fit2p and Fit3p, proteins involved in iron retention within the yeast cell wall, were markedly increased by treatment of Saccharomyces cerevisiae with cisplatin. Expression of FIT2 and FIT3 is known to be transcriptionally regulated by Aft1p. Northern blotting demonstrated a time- and concentration-dependent increase in the mRNA levels of both proteins following treatment with cisplatin. However, overexpression or disruption of the FIT2 or FIT3 genes had little effect on the susceptibility of yeast to cisplatin. Although Fit2p and Fit3p do not appear to be directly involved in protecting against the toxic effects of cisplatin, the present results suggest the existence of an activation system of gene expression in response to cisplatin within yeast cells.
cDNA微阵列分析表明,参与酵母细胞壁内铁保留的蛋白质Fit2p和Fit3p的mRNA水平,在酿酒酵母用顺铂处理后显著增加。已知FIT2和FIT3的表达受Aft1p转录调控。Northern印迹法显示,顺铂处理后,这两种蛋白质的mRNA水平呈时间和浓度依赖性增加。然而,FIT2或FIT3基因的过表达或缺失对酵母对顺铂的敏感性影响很小。尽管Fit2p和Fit3p似乎不直接参与抵抗顺铂的毒性作用,但目前的结果表明酵母细胞内存在一个响应顺铂的基因表达激活系统。