Scherzinger E, Lanka E, Hillenbrand G
Nucleic Acids Res. 1977 Dec;4(12):4151-63. doi: 10.1093/nar/4.12.4151.
Bacteriophage T7 DNA primase (gene-4 protein, 66,000 daltons) enables T7 DNA polymerase to initiate the synthesis of DNA chains on single-stranded templates. An initial step in the process of chain initiation is the formation of an oligoribonucleotide primer by T7 primase. The enzyme, in the presence of natural SS DNA, Mg++ (or Mn++), ATP and CTP (or a mixture of all 4 rNTPs), catalyzes the synthesis of di-, tri-, and tetraribonucleotides all starting at the 5' terminus with pppA. In a subsequent step requiring both T7 DNA polymerase and primase, the short oligoribonucleotides (predominantly pppA-C-C-AOH) are extended by covalent addition of deoxyribonucleotides. With the aid of primase, T7 DNA polymerase can also utilize efficiently a variety of synthetic tri-, tetra-, or pentanucleotides as chain initiators. T7 primase apparently plays an active role in primer extension by stabilizing the short primer segments in a duplex state on the template DNA.
噬菌体T7 DNA引发酶(基因4蛋白,66,000道尔顿)可使T7 DNA聚合酶在单链模板上起始DNA链的合成。链起始过程的第一步是由T7引发酶形成寡核糖核苷酸引物。该酶在天然单链DNA、Mg++(或Mn++)、ATP和CTP(或所有4种核糖核苷三磷酸的混合物)存在的情况下,催化合成均以pppA起始于5'末端的二核糖核苷酸、三核糖核苷酸和四核糖核苷酸。在随后需要T7 DNA聚合酶和引发酶的步骤中,短寡核糖核苷酸(主要是pppA-C-C-AOH)通过脱氧核糖核苷酸的共价添加而延伸。借助引发酶,T7 DNA聚合酶还能够有效地利用多种合成的三核糖核苷酸、四核糖核苷酸或五核糖核苷酸作为链起始物。T7引发酶显然通过将短引物片段稳定在模板DNA上的双链状态而在引物延伸中发挥积极作用。