Suzuki H, Suzuki S, Kumar S, Ozawa T
Department of Biomedical Chemistry, Faculty of Medicine, University of Nagoya, Japan.
Biochem Biophys Res Commun. 1995 Aug 4;213(1):204-10. doi: 10.1006/bbrc.1995.2117.
We have found that Mt element-binding proteins (MtEBPs) with the same binding capability are present in the nuclei and mitochondria of human, bovine, and rat cells. MtEBPs purified from the human nuclei and mitochondria with Mt element-specific DNA affinity chromatography contained 4 different polypeptides, respectively. A UV-induced DNA cross-linking study showed that 47- or 55-kDa of the nuclear MtEBP recognizes Mt in the 5'-flanking region of the human cytochrome c1 gene and that both 140- and 180-kDa polypeptides of the mitochondrial (mt) MtEBPs bind Mts in the human mt promoter region. Mt MtEBPs recognized a Mt4 element-like sequence within the mt transcription factor A binding site for the heavy-strand promoter. These results suggest a MtEBP-mediated coordination mechanism between nuclear and mt genetic systems.
我们发现,具有相同结合能力的线粒体元件结合蛋白(MtEBPs)存在于人类、牛和大鼠细胞的细胞核和线粒体中。通过线粒体元件特异性DNA亲和层析从人类细胞核和线粒体中纯化得到的MtEBPs分别包含4种不同的多肽。紫外线诱导的DNA交联研究表明,47 kDa或55 kDa的细胞核MtEBP识别人类细胞色素c1基因5'侧翼区域中的线粒体元件,而线粒体(mt)MtEBPs的140 kDa和180 kDa多肽均与人线粒体启动子区域中的线粒体元件结合。线粒体MtEBPs识别重链启动子的线粒体转录因子A结合位点内的一个类似线粒体元件4的序列。这些结果提示了一种由MtEBP介导的核遗传系统与线粒体遗传系统之间的协调机制。