Yamaguchi-Iwai Y, Stearman R, Dancis A, Klausner R D
Cell Biology and Metabolism Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.
EMBO J. 1996 Jul 1;15(13):3377-84.
Iron deprivation of Saccharomyces cerevisiae induces transcription of genes required for high-affinity iron uptake. AFT1 mediates this transcriptional control. In this report, the 5'-flanking region of FET3, which encodes a copper-dependent oxidase required for iron transport, was analyzed and found to contain a DNA sequence responsible for AFT1-regulated gene expression. AFT1 was capable of interacting specifically with this DNA sequence. A core element within this DNA sequence necessary for the binding of AFT1 was also determined. In vivo footprinting demonstrated occupancy of the AFT1 binding site in cells deprived of iron and not in cells grown in the presence of iron. Thus, the environmental signal resulting from iron deprivation was transduced through the regulated binding of AFT1 to the FET3 promoter, followed by the activation of transcription. A regulon of genes under the control of AFT1 could be defined. AFT1 was able to bind to a consensus binding site (PyPuCACCCPu) in the 5' region of FRE1, FRE2, FTR1, FTH1 and CCC2.
酿酒酵母缺铁会诱导高亲和力铁摄取所需基因的转录。AFT1介导这种转录调控。在本报告中,对编码铁转运所需铜依赖性氧化酶的FET3的5'侧翼区域进行了分析,发现其包含一个负责AFT1调控基因表达的DNA序列。AFT1能够与该DNA序列特异性相互作用。还确定了该DNA序列中AFT1结合所必需的核心元件。体内足迹分析表明,缺铁细胞中AFT1结合位点被占据,而在铁存在下生长的细胞中则未被占据。因此,缺铁产生的环境信号通过AFT1与FET3启动子的调控结合进行转导,随后激活转录。可以定义一个受AFT1控制的基因调控子。AFT1能够与FRE1、FRE2、FTR1、FTH1和CCC2的5'区域中的共有结合位点(PyPuCACCCPu)结合。