Naganuma A, Miura N, Kaneko S, Mishina T, Hosoya S, Miyairi S, Furuchi T, Kuge S
Laboratory of Molecular and Biochemical Toxicology, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Japan.
FASEB J. 2000 May;14(7):968-72. doi: 10.1096/fasebj.14.7.968.
Using a genomic library constructed from Saccharomyces cerevisiae, we have identified a gene GFA1 that confers resistance to methylmercury toxicity. GFA1 encodes L-glutamine:D-fructose-6-phosphate amidotransferase (GFAT) and catalyzes synthesis of glucosamine-6-phosphate. Transformed yeast cells expressing GFA1 demonstrated resistance to methylmercury but no resistance to p-chloromercuribenzoate, a GFAT inhibitor. The cytotoxicity of methylmercury was inhibited by loading excess glucosamine 6-phosphate into yeast. Considering that GFAT is an essential cellular enzyme, our findings suggest that GFAT is the major target molecule of methylmercury in yeasts. This report is the first to identify the target molecule of methylmercury toxicity in eukaryotic cells.
利用从酿酒酵母构建的基因组文库,我们鉴定出了一个赋予对甲基汞毒性抗性的基因GFA1。GFA1编码L-谷氨酰胺:D-果糖-6-磷酸酰胺转移酶(GFAT),并催化6-磷酸葡糖胺的合成。表达GFA1的转化酵母细胞对甲基汞具有抗性,但对GFAT抑制剂对氯汞苯甲酸没有抗性。通过向酵母中加载过量的6-磷酸葡糖胺可抑制甲基汞的细胞毒性。鉴于GFAT是一种必需的细胞酶,我们的研究结果表明GFAT是酵母中甲基汞的主要靶分子。本报告首次鉴定出真核细胞中甲基汞毒性的靶分子。