Imbert J, Zafarullah M, Culotta V C, Gedamu L, Hamer D
Laboratory of Biochemistry, National Cancer Institute, Bethesda, Maryland 20892.
Mol Cell Biol. 1989 Dec;9(12):5315-23. doi: 10.1128/mcb.9.12.5315-5323.1989.
Metallothionein (MT) gene promoters in higher eucaryotes contain multiple metal regulatory elements (MREs) that are responsible for the metal induction of MT gene transcription. We identified and purified to near homogeneity a 74-kilodalton mouse nuclear protein that specifically binds to certain MRE sequences. This protein, MBF-I, was purified employing as an affinity reagent a trout MRE that is shown to be functional in mouse cells but which lacks the G+C-rich and SP1-like sequences found in many mammalian MT gene promoters. Using point-mutated MREs, we showed that there is a strong correlation between DNA binding in vitro and MT gene regulation in vivo, suggesting a direct role of MBF-I in MT gene transcription. We also showed that MBF-I can induce MT gene transcription in vitro in a mouse extract and that this stimulation requires zinc.
高等真核生物中的金属硫蛋白(MT)基因启动子含有多个金属调节元件(MRE),这些元件负责MT基因转录的金属诱导。我们鉴定并纯化出一种74千道尔顿的小鼠核蛋白,该蛋白能特异性结合某些MRE序列,纯度接近均一。这种蛋白,即MBF-I,是利用鳟鱼MRE作为亲和试剂纯化得到的。该鳟鱼MRE在小鼠细胞中具有功能,但缺乏许多哺乳动物MT基因启动子中富含G+C的序列和类似SP1的序列。使用点突变的MRE,我们发现体外DNA结合与体内MT基因调控之间存在很强的相关性,这表明MBF-I在MT基因转录中起直接作用。我们还表明,MBF-I可以在小鼠提取物中体外诱导MT基因转录,并且这种刺激需要锌。