Nakagawa C W, Yamada K, Mutoh N
Department of Genetics, Institute for Developmental Research, Kagiya-cho, Kasugai, Aichi 480-0392, Japan.
J Biochem. 2000 Feb;127(2):233-8. doi: 10.1093/oxfordjournals.jbchem.a022599.
We examined the induction of the catalase gene (ctt1(+)) of fission yeast Schizosaccharomyces pombe in response to several stresses by using mutants of transcription factors (Atf1 and Pap1) and a series of deletion mutants of the ctt1(+) promoter region. A transcription factor, Atf1, and its binding site are necessary for the induction of ctt1(+) by osmotic stress, UV irradiation, and heat shock. Induction by menadione treatment, which produces superoxide anion, required element A, the region from -111 to -90 (numbered with the transcription start site as +1). The factor responsible for the induction of the gene by oxidative stress via element A was identified as the transcription factor Pap1. We also found that Atf1 is activated by menadione treatment in pap1 mutant cells, although it is not activated by menadione treatment in pap1(+) cells. The activity of catalase is not increased in pap1 cells by several stresses, despite mRNA induction, suggesting that Pap1 plays some role in the expression of catalase activity.
我们通过使用转录因子(Atf1和Pap1)的突变体以及ctt1(+)启动子区域的一系列缺失突变体,研究了裂殖酵母粟酒裂殖酵母过氧化氢酶基因(ctt1(+))在几种应激反应中的诱导情况。转录因子Atf1及其结合位点对于渗透应激、紫外线照射和热休克诱导ctt1(+)是必需的。甲萘醌处理产生超氧阴离子,其诱导需要元件A,即从-111到-90的区域(以转录起始位点为+1编号)。通过元件A介导氧化应激诱导该基因的因子被鉴定为转录因子Pap1。我们还发现,在pap1突变体细胞中,Atf1可被甲萘醌处理激活,尽管在pap1(+)细胞中它不会被甲萘醌处理激活。尽管mRNA被诱导,但在pap1细胞中,几种应激均不会使过氧化氢酶活性增加,这表明Pap1在过氧化氢酶活性的表达中发挥了一定作用。