Kawasaki K, Enomoto T, Suzuki M, Seki M, Hanaoka F, Yamada M
Biochemistry. 1986 May 20;25(10):3044-50. doi: 10.1021/bi00358a046.
A novel factor that stimulates DNA polymerase alpha activity on poly(dA) X oligo(dT) has been identified and partially purified from mouse FM3A cells. The assay system for the factor contained poly(ethylene glycol) 6000. The activities of DNA polymerase alpha on poly(dA) X oligo(dT) in the presence and absence of the stimulating factor were increased greatly by the addition of poly(ethylene glycol). Stimulation by the factor was observed at all the primer to template ratios tested from 0.01 to 0.3. The highest activity was observed at the ratio of 0.05, corresponding to about 3.3 primers on one template in the presence of the factor. The concentration of DNA polymerase alpha used in the assay affected the stimulation by the factor, and the stimulation became more prominent at concentrations of the enzyme lower than 0.04 unit per assay. The stimulating factor lowered the Km value of DNA polymerase alpha for the template-primer, though they had no effect on the Km value for dTTP substrate. The results of product analysis suggested that the stimulation by the factor is mainly due to the increase in the initiation frequency of DNA synthesis from the primers. The stimulating factor specifically stimulated DNA polymerase alpha but not DNA polymerases beta and gamma. Furthermore, the factor formed a complex with DNA polymerase alpha under a certain condition.
一种能刺激聚(dA)×寡聚(dT)上DNA聚合酶α活性的新因子已从小鼠FM3A细胞中被鉴定并部分纯化。该因子的检测系统含有聚乙二醇6000。添加聚乙二醇后,无论有无刺激因子,聚(dA)×寡聚(dT)上DNA聚合酶α的活性都大幅增加。在从0.01到0.3的所有测试引物与模板比例下,均观察到该因子的刺激作用。在0.05的比例下观察到最高活性,在有该因子存在时,相当于一个模板上约有3.3个引物。检测中使用的DNA聚合酶α的浓度影响该因子的刺激作用,在酶浓度低于每次检测0.04单位时,刺激作用更显著。该刺激因子降低了DNA聚合酶α对模板引物的Km值,不过对dTTP底物的Km值没有影响。产物分析结果表明,该因子的刺激作用主要是由于引物引发DNA合成的起始频率增加。该刺激因子特异性地刺激DNA聚合酶α,而不刺激DNA聚合酶β和γ。此外,该因子在一定条件下与DNA聚合酶α形成复合物。