Conaway R C, Lehman I R
Proc Natl Acad Sci U S A. 1982 Aug;79(15):4585-8. doi: 10.1073/pnas.79.15.4585.
The primase associated with the DNA polymerase alpha from embryos of Drosophila melanogaster catalyzes the synthesis of ribo-oligonucleotide primers on single-stranded M13 DNA or polydeoxythymidylate templates, which can be elongated by DNA polymerase action [Conaway, R. C. & Lehman, I. R. (1982) Proc, Natl. Acad. Sci, USA 79, 2523--2527]. The primers synthesized in a coupled primase-DNA polymerase alpha reaction with an M13 DNA template are of a unique size (15 residues); those synthesized with poly(dT) range from 8 to 15 nucleotides. Primer synthesis is initiated at multiple but nonrandom sites. Like the DNA primase of Escherichia coli and the comparable activity in intact nuclei of polyoma-infected mouse cells, the DNA primase of D. melanogaster can substitute deoxynucleotides for ribonucleotides during primer synthesis.
与黑腹果蝇胚胎中的DNA聚合酶α相关的引发酶催化在单链M13 DNA或聚脱氧胸苷酸模板上合成核糖寡核苷酸引物,这些引物可通过DNA聚合酶作用进行延伸[康纳韦,R.C. & 莱曼,I.R.(1982年)《美国国家科学院院刊》79,2523 - 2527]。在与M13 DNA模板的偶联引发酶 - DNA聚合酶α反应中合成的引物具有独特的大小(15个残基);用聚(dT)合成的引物长度范围为8至15个核苷酸。引物合成在多个但非随机的位点起始。与大肠杆菌的DNA引发酶以及多瘤病毒感染的小鼠细胞完整细胞核中的类似活性一样,黑腹果蝇的DNA引发酶在引物合成过程中可以用脱氧核苷酸替代核糖核苷酸。