Sims J, Benz E W
Proc Natl Acad Sci U S A. 1980 Feb;77(2):900-4. doi: 10.1073/pnas.77.2.900.
The dnaG protein of Escherichia coli initiates DNA replication by synthesizing primer oligonucleotides for elongation by DNA polymerae. The experiments reported here probe the nature of the nucleic acid element recognized by the dnaG protein. Three well-separated groups of nucleotides within the negative-strand origin of the single-stranded phage phi K are protected by the dnaG protein against nuclease digestion. DNA as far as 115 bases from the start site of primer synthesis is involved in binding of the dnaG protein to the replication origin. One molecule of dnaG protein could protect all of these nucleotides if the DNA were folded into a higher-order tertiary structure. Protection of the phi K origin by dnaG protein requires DNA binding protein, and it does not occur if the group of protected nucleotides most distant from the start site is removed from the template. There is no binding of dnaG protein to the complementary strand of the phi K origin-region DNA. The observed protection of the positive strand is due to a functional nucleic acid-protein complex.
大肠杆菌的dnaG蛋白通过合成引物寡核苷酸来启动DNA复制,以便DNA聚合酶进行延伸。本文报道的实验探究了dnaG蛋白识别的核酸元件的性质。单链噬菌体phi K负链起源内三个间隔良好的核苷酸组受到dnaG蛋白的保护,免受核酸酶消化。从引物合成起始位点起多达115个碱基的DNA参与了dnaG蛋白与复制起点的结合。如果DNA折叠成更高阶的三级结构,一个dnaG蛋白分子就能保护所有这些核苷酸。dnaG蛋白对phi K起点的保护需要DNA结合蛋白,如果从模板中去除距离起始位点最远的受保护核苷酸组,这种保护就不会发生。dnaG蛋白不会与phi K起点区域DNA的互补链结合。观察到的正链保护是由于功能性核酸 - 蛋白质复合物所致。