Westin G, Schaffner W
Institut für Molekularbiologie II der Universität Zürich, Switzerland.
EMBO J. 1988 Dec 1;7(12):3763-70. doi: 10.1002/j.1460-2075.1988.tb03260.x.
Heavy metal ions are effective inducers of metallothionein gene transcription. The metal response is dependent on short DNA motifs, so-called MREs (metal responsive elements) that occur in multiple copies in the promoter region of these genes. We have analysed an MRE of the mouse metallothionein-I gene (MREd) and we demonstrate that this can function over long distances as a bona fide metal ion-inducible enhancer. The transcription factor Sp1 and a zinc-inducible factor, designated MTF-1, bind to the MREd enhancer in vitro. The combined use of MREd mutants in a transient assay in HeLa cells and a competition band shift assay show that the zinc-inducible formation of the MTF-1/DNA complex in vitro correlates with zinc-inducible transcription in vivo. A chemical methylation interference assay revealed remarkably similar but non-identical guanine interference patterns for the MTF-1 and Sp1 complexes, which may mean that MTF-1 is related to the Sp1 factor.
重金属离子是金属硫蛋白基因转录的有效诱导剂。金属反应取决于短的DNA基序,即所谓的MREs(金属反应元件),这些元件在这些基因的启动子区域以多个拷贝出现。我们分析了小鼠金属硫蛋白-I基因的一个MRE(MREd),并证明它可以作为一个真正的金属离子诱导增强子在长距离上发挥作用。转录因子Sp1和一个锌诱导因子,命名为MTF-1,在体外与MREd增强子结合。在HeLa细胞的瞬时分析中联合使用MREd突变体和竞争带移分析表明,体外MTF-1/DNA复合物的锌诱导形成与体内锌诱导转录相关。化学甲基化干扰分析揭示了MTF-1和Sp1复合物显著相似但不完全相同的鸟嘌呤干扰模式,这可能意味着MTF-1与Sp1因子有关。