Sa Jae-Hoon, Shin Youn Hee, Lim Hye Won, Kim Kyunghoon, Park Eun-Hee, Lim Chang-Jin
Division of Life Sciences, Kangwon National University, Chuncheon 200-701, Korea.
Mol Cells. 2002 Dec 31;14(3):444-8.
A third gene that encodes glutathione S-transferase (GSTIII) was previously cloned from the fission yeast Schizosaccharomyces pombe. Using the GSTIII-lacZ fusion plasmid pGDA-19, its expression was shown to be enhanced by various metal ions. In the present study, four additional fusion plasmids, pGDA-29, pGDA-39, PGDA-49, and pGDA-59, were designed to carry 998, 378, 276, and 115 bp upstream regions from the translational initiation point, respectively. The major activation region was located between -998 and -378 bp upstream of the GSTIII gene. Regulatory sequences that are responsible for the induction by metal ions reside between -998 and -378 bp and between -276 and -115 bp upstream of the gene. The overexpressed Pap1 exerts a repression effect on the GSTIII expression via -998 to approximately -378 bp region, whereas it exerts an activation effect on the GSTIII expression via -270 to approximately -115 bp region. However, the induction of the GSTIII gene by metal ions occurs independent of Pap1.
第三个编码谷胱甘肽S-转移酶(GSTIII)的基因先前是从裂殖酵母粟酒裂殖酵母中克隆得到的。使用GSTIII-lacZ融合质粒pGDA-19,研究表明其表达可被多种金属离子增强。在本研究中,设计了另外四个融合质粒pGDA-29、pGDA-39、PGDA-49和pGDA-59,分别携带翻译起始点上游998、378、276和115 bp的区域。主要激活区域位于GSTIII基因上游-998至-378 bp之间。负责金属离子诱导的调控序列位于该基因上游-998至-378 bp之间以及-276至-115 bp之间。过表达的Pap1通过-998至约-378 bp区域对GSTIII表达发挥抑制作用,而通过-270至约-115 bp区域对GSTIII表达发挥激活作用。然而,金属离子对GSTIII基因的诱导独立于Pap1发生。