Ghivizzani S C, Madsen C S, Nelen M R, Ammini C V, Hauswirth W W
Department of Immunology and Medical Microbiology, University of Florida, College of Medicine, Gainesville 32610-0266.
Mol Cell Biol. 1994 Dec;14(12):7717-30. doi: 10.1128/mcb.14.12.7717-7730.1994.
Using in organello footprint analysis, we demonstrate that within human placental mitochondria there is a high level of protein-DNA binding at regularly phased intervals throughout a 500-bp region encompassing the D-loop DNA origins and two promoter regions. Comparison with in vitro DNase I protection studies indicates that this protein-DNA interaction is due to non-sequence-specific binding by human mitochondrial transcription factor A (h-mtTFA). Since h-mtTFA can bend and wrap DNA, like its yeast counterpart ABF2, a primary function of h-mtTFA appears to be specific packaging of the mitochondrial DNA control region in vivo. Intervals of protein binding coincide with the spacing of the RNA start sites and prominent D-loop DNA 5' ends, suggesting a role for phased h-mtTFA binding in defining transcription and H-strand DNA replication origins. Significant protein-DNA interaction was also observed within the human homolog of conserved sequence block 1, both in organello and in vitro, using purified h-mtTFA.
通过细胞器内足迹分析,我们证明在人胎盘线粒体中,在一个包含D环DNA起源和两个启动子区域的500碱基对区域内,蛋白质与DNA的结合在规则间隔处以高水平存在。与体外DNase I保护研究的比较表明,这种蛋白质与DNA的相互作用是由于人类线粒体转录因子A(h-mtTFA)的非序列特异性结合。由于h-mtTFA可以像其酵母对应物ABF2一样使DNA弯曲和缠绕,h-mtTFA的主要功能似乎是在体内对线粒体DNA控制区域进行特异性包装。蛋白质结合的间隔与RNA起始位点和突出的D环DNA 5'端的间距一致,这表明阶段性的h-mtTFA结合在定义转录和H链DNA复制起源中起作用。使用纯化的h-mtTFA,在细胞器内和体外的保守序列块1的人类同源物中也观察到了显著的蛋白质与DNA相互作用。