Kim Su-Jung, Kim Hong-Gyum, Kim Byung-Chul, Park Eun-Hee, Lim Chang-Jin
Division of Life Sciences, Kangwon National University, Chuncheon 200-701, Korea.
Mol Cells. 2004 Oct 31;18(2):242-8.
Glutathione (GSH), an important antioxidant involved in the stress response, is synthesized in two sequential reactions involving glutamylcysteine synthetase (GCS), followed by glutathione synthetase (GS). Expression of the unique GS gene in the fission yeast Schizosaccharomyces pombe was previously found to be regulated by nitric oxide and by L-buthionine-(S,R)-sulfoximine (BSO), a specific inhibitor of GCS. In this work, expression of S. pombe GS gene is shown to be induced by menadione (MD), which generates superoxide. The responsible DNA sequence between -365 and -234 bp from the translation start site, was convinced using five GS-lacZ fusion plasmids. Expression of GS gene is also induced by low glucose, fructose and disaccharides, apparently dependent on Pap1 protein; GS mRNA increases in low concentrations of glucose in wild type S. pombe but not in Pap1-negative cells. Although nonfermentable carbon sources such as acetate and ethanol stimulate expression of GS gene, they also arrest the growth of the yeast cells. These results indicate that the biosynthesis of glutathione is regulated by superoxide radicals and carbon source limitation.
谷胱甘肽(GSH)是一种参与应激反应的重要抗氧化剂,它通过两个连续反应合成,这两个反应涉及谷氨酰半胱氨酸合成酶(GCS),随后是谷胱甘肽合成酶(GS)。先前发现,裂殖酵母粟酒裂殖酵母中独特的GS基因的表达受一氧化氮和L-丁硫氨酸-(S,R)-亚砜亚胺(BSO,一种GCS的特异性抑制剂)的调节。在这项研究中,粟酒裂殖酵母GS基因的表达显示受甲萘醌(MD)诱导,MD可产生超氧化物。利用五个GS-lacZ融合质粒确定了翻译起始位点上游-365至-234 bp之间的负责DNA序列。GS基因的表达也受低浓度葡萄糖、果糖和双糖诱导,这显然依赖于Pap1蛋白;在野生型粟酒裂殖酵母中,低浓度葡萄糖会使GS mRNA增加,但在Pap1阴性细胞中则不会。尽管不可发酵碳源(如乙酸盐和乙醇)会刺激GS基因的表达,但它们也会使酵母细胞的生长停滞。这些结果表明,谷胱甘肽的生物合成受超氧自由基和碳源限制的调节。