Scherzinger E, Lanka E, Morelli G, Seiffert D, Yuki A
Eur J Biochem. 1977 Feb;72(3):543-58. doi: 10.1111/j.1432-1033.1977.tb11278.x.
The T7gene-4 protein has been purified to near homogeneity using a complementation assay in vitro, and it is designated T7 DNA-priming protein (DNA primase). The purified enzyme enables T7 DNA polymerase to initate DNA synthesis on various circular single-stranded DNA templates by a mechanism which involes the synthesis of a very short RNA primer. The oligoribonucleotide, which is linked to the product DNA via a 3':5'-phosphodiester bond, starts with pppA-C and terminates predominantly with AMP. When only ATP and CPT are precursors, the RNA primer is found to be primarily a tetranucleotide of the sequence pppA-C-C-A. Using oligoribonucleotides in place of ribonucleoside triphosphates as chain initators, T7 DNA-priming protein drastically increases the efficiency with which T7 DNA polymerase can utilize particular tetranucleotide primers containing A and C residues. T7 DNA-priming protein also enables T7 DNA polymerase to make use of native or nicked duplex T7 DNA as template-primer. This reaction does not require ribonucleoside triphosphates, although their addition enhances DNA synthesis 2--4 fold. The product formed in their absence is covalently attached to the template DNA and is found to contain a few long branches when examined by electron microscopy. In the presence of ribonucleoside triphosphates most of the newly made product arises from imitation of DNA chains de novo. Incubation of three proteins: T7 DNA-priming protein, T7 DNA polymerase, and T7 DNA-binding protein, with ribonucleoside and deoxyribonucleoside triphosphates, and with phiX174DNA as template leads to the generation of 'rolling circle-like' structures as visualized in the electron microscope. Single-stranded regions at the tail-circle junction indicate that initations can occur de novo on the displaced complementary strand. This is consistent with a discontinuous mode of 'lagging' strand synthesis and suggests that the same proteins may also be responsible for fork propagation in vivo.
利用体外互补分析,已将T7基因4蛋白纯化至近乎均一,并将其命名为T7 DNA引发蛋白(DNA引发酶)。纯化后的酶可使T7 DNA聚合酶通过一种涉及合成极短RNA引物的机制,在各种环状单链DNA模板上起始DNA合成。通过3':5'-磷酸二酯键与产物DNA相连的寡核糖核苷酸,起始于pppA-C,主要以AMP结尾。当仅ATP和CTP作为前体时,发现RNA引物主要是序列为pppA-C-C-A的四核苷酸。使用寡核糖核苷酸代替核糖核苷三磷酸作为链引发剂,T7 DNA引发蛋白可显著提高T7 DNA聚合酶利用含有A和C残基的特定四核苷酸引物的效率。T7 DNA引发蛋白还可使T7 DNA聚合酶利用天然或带切口的双链T7 DNA作为模板引物。该反应不需要核糖核苷三磷酸,不过添加它们可使DNA合成提高2至4倍。在没有核糖核苷三磷酸的情况下形成的产物与模板DNA共价连接,通过电子显微镜检查发现含有一些长分支。在有核糖核苷三磷酸存在时,大多数新合成的产物源于DNA链的从头起始。将T7 DNA引发蛋白、T7 DNA聚合酶和T7 DNA结合蛋白这三种蛋白与核糖核苷和脱氧核糖核苷三磷酸一起孵育,并以φX174DNA作为模板,在电子显微镜下可观察到产生“滚环样”结构。尾环连接处的单链区域表明从头起始可发生在被置换的互补链上。这与“滞后”链合成的不连续模式一致,并表明相同的蛋白在体内可能也负责叉的延伸。