Moon Jeong-Su, Lim Hye-Won, Park Eun-Hee, Lim Chang-Jin
Division of Life Sciences, College of Natural Sciences, Kangwon National University, Chuncheon 200-701, Korea.
Mol Cells. 2005 Aug 31;20(1):74-82.
Glutaredoxins (Grxs) are thioloxidoreductases which are required for maintaining thiol/disulfide equilibrium in living cells. The Grx3 gene, which encodes one of the three monothiol Grxs in the fission yeast Schizosaccharomyces pombe, was characterized, and its transcriptional regulation studied. Genomic DNA encoding Grx3 was isolated by PCR, and a plasmid pTT3 carrying this DNA was produced. The DNA sequence has 1,267 bp, which would encode a monothiol Grx of 166 amino acids with a molecular mass of 18.3 kDa. The putative protein has 27% homology with Grx5, and contains many hydrophobic amino acid residues in its N-terminal region. S. pombe cells harboring pTT3 had increased Grx activity and enhanced survival on minimal medium plates containing aluminum (5 mM), BSO (0.05 mM), menadione (0.01 mM) or cadmium (0.2 mM). The 568 bp upstream region of Grx3 was fused into the promoterless beta-galactosidase gene of the shuttle vector YEp367R to generate fusion plasmid pMJS10. Potassium chloride (KCl) and metals including aluminum and cadmium enhanced the synthesis of beta-galactosidase from the fusion gene. The synthesis of beta-galactosidase was also enhanced, in a Pap1-dependent manner, by fermentable carbon sources such as glucose (at low concentrations) and sucrose, but not by non-fermentable carbon sources such as ethanol and acetate. Grx3 mRNA increased in response to treatment with BSO. These observations indicate that S. pombe Grx3 is involved in the response to stress, and is regulated by stress.
谷氧还蛋白(Grxs)是硫醇氧化还原酶,对于维持活细胞中的硫醇/二硫键平衡是必需的。对编码粟酒裂殖酵母中三种单硫醇谷氧还蛋白之一的Grx3基因进行了表征,并研究了其转录调控。通过PCR分离出编码Grx3的基因组DNA,并构建了携带该DNA的质粒pTT3。该DNA序列有1267 bp,可编码一个由166个氨基酸组成的单硫醇谷氧还蛋白,分子量为18.3 kDa。该推定蛋白与Grx5有27%的同源性,并且在其N端区域含有许多疏水氨基酸残基。携带pTT3的粟酒裂殖酵母细胞在含有铝(5 mM)、丁硫氨酸亚砜胺(BSO,0.05 mM)、甲萘醌(0.01 mM)或镉(0.2 mM)的基本培养基平板上具有增强的谷氧还蛋白活性和更高的存活率。将Grx3上游568 bp的区域与穿梭载体YEp367R的无启动子β-半乳糖苷酶基因融合,以产生融合质粒pMJS10。氯化钾(KCl)以及包括铝和镉在内的金属增强了融合基因β-半乳糖苷酶的合成。β-半乳糖苷酶的合成也以Pap1依赖的方式,被可发酵碳源如葡萄糖(低浓度)和蔗糖增强,但不被非可发酵碳源如乙醇和乙酸增强。用BSO处理后,Grx3 mRNA增加。这些观察结果表明,粟酒裂殖酵母Grx3参与应激反应,并受到应激的调控。