Cho Young-Wook, Park Eun-Hee, Fuchs James A, Lim Chang-Jin
Division of Life Sciences, College of Natural Sciences, Kangwon National University, Chuncheon 200-701, South Korea.
Biochim Biophys Acta. 2002 Apr 12;1574(3):399-402. doi: 10.1016/s0167-4781(01)00363-3.
A second glutathione S-transferase gene (GST II) was isolated from the chromosomal DNA of the fission yeast Schizosaccharomyces pombe. The nucleotide sequence determined contains 1908 bp including an open reading frame of 230 amino acids that would encode a protein of a molecular mass of 26843.4 Da. The amino acid sequence of the putative GST II is very homologous with that of the previously isolated GST gene (GST I) located in the same chromosome III of S. pombe. The cloned GST II gene produces the functional GST in S. pombe, and it gives much higher GST in the stationary phase than in the exponential phase. Regulation of the GST II gene was studied using the GST II-lacZ fusion. The synthesis of beta-galactosidase from the fusion plasmid is greatly enhanced by the treatments with oxidative stresses such as menadione and mercuric chloride. It is also induced by o-dinitrobenzene, one of the GST substrates. NO-generating S-nitroso-N-acetylpenicillamine has a weak induction effect on the expression of GST II gene. These results indicate that the S. pombe GST II gene is involved in the oxidative stress response and detoxification. However, physiological meaning on the existence of the two similar GST genes in S. pombe remains unknown yet.
从裂殖酵母粟酒裂殖酵母的染色体DNA中分离出了第二个谷胱甘肽S-转移酶基因(GST II)。所测定的核苷酸序列包含1908个碱基对,其中包括一个230个氨基酸的开放阅读框,该开放阅读框将编码一个分子量为26843.4道尔顿的蛋白质。推测的GST II的氨基酸序列与先前在粟酒裂殖酵母的同一III号染色体上分离出的GST基因(GST I)的氨基酸序列高度同源。克隆的GST II基因在粟酒裂殖酵母中产生功能性的GST,并且它在稳定期产生的GST比在指数期产生的GST要高得多。使用GST II-lacZ融合体研究了GST II基因的调控。用甲萘醌和氯化汞等氧化应激处理可大大增强融合质粒中β-半乳糖苷酶的合成。它也由GST底物之一邻二硝基苯诱导。产生NO的S-亚硝基-N-乙酰青霉胺对GST II基因的表达有较弱的诱导作用。这些结果表明,粟酒裂殖酵母GST II基因参与氧化应激反应和解毒作用。然而,粟酒裂殖酵母中两个相似的GST基因存在的生理意义仍然未知。