Madsen C S, Ghivizzani S C, Hauswirth W W
Department of Immunology and Medical Microbiology, University of Florida, Gainesville 32610.
Mol Cell Biol. 1993 Apr;13(4):2162-71. doi: 10.1128/mcb.13.4.2162-2171.1993.
A methylation protection assay was used in a novel manner to demonstrate a specific bovine protein-mitochondrial DNA (mtDNA) interaction within the organelle (in organello). The protected domain, located near the D-loop 3' end, encompasses a conserved termination-associated sequence (TAS) element which is thought to be involved in the regulation of mtDNA synthesis. In vitro footprinting studies using a bovine mitochondrial extract and a series of deleted mtDNA templates identified a approximately 48-kDa protein which binds specifically to a single TAS element also protected within the mitochondrion. Because other TAS-like elements located in close proximity to the protected region did not footprint, protein binding appears to be highly sequence specific. The in organello and in vitro data, together, provide evidence that D-loop formation is likely to be mediated, at least in part, through a trans-acting factor binding to a conserved sequence element located 58 bp upstream of the D-loop 3' end.
采用一种全新的甲基化保护分析方法,在细胞器(原位)中证明了一种特定的牛蛋白质与线粒体DNA(mtDNA)之间的相互作用。受保护区域位于D环3'端附近,包含一个保守的终止相关序列(TAS)元件,该元件被认为参与mtDNA合成的调控。使用牛线粒体提取物和一系列缺失的mtDNA模板进行的体外足迹研究,鉴定出一种约48 kDa的蛋白质,它能特异性结合线粒体中也受到保护的单个TAS元件。由于位于受保护区域附近的其他类似TAS的元件没有足迹,蛋白质结合似乎具有高度的序列特异性。原位和体外数据共同提供了证据,表明D环的形成可能至少部分是通过一种反式作用因子与位于D环3'端上游58 bp处的保守序列元件结合来介导的。