Chuang R Y, Chuang L F
Proc Natl Acad Sci U S A. 1975 Aug;72(8):2935-9. doi: 10.1073/pnas.72.8.2935.
The mechanism of the effect of an RNA polymerase II (RNA nucleotidyltransferase II) stimulation factor isolated from the nuclei of chicken myeloblastosis cells was studied. The stimulation requires the presence of all four nucleoside triphosphates and depends upon an exogenous DNA template. In the absence of the factor, RNA synthesis ceases after 20-30 min, but in the presence of the factor, synthesis continues up to 60-80 min. Addition of the factor at 35 min after incubation causes resumption of RNA synthesis. The factor greatly stimulates the activity of RNA polymerase II at low enzyme concentrations. The RNA polymerase activity is more sensitive to alpha-amanitin inhibition when the factor is present. Experiments of [gamma-32P]ATP incorporation reveal that the factor provides for an increased frequency of initiation of RNA chains, both of the primary initiation events and re-initiation after previous ones were completed. A slightly higher rate of RNA chain growth was also observed with this factor but the ultimate size of RNA synthesized was not affected, as determined by formaldehyde/sucrose gradient centrifugation. These data suggest that the factor functions at the initiation stages of the RNA polymerase reaction.
对从鸡成髓细胞瘤细胞核中分离出的一种RNA聚合酶II(RNA核苷酸转移酶II)刺激因子的作用机制进行了研究。这种刺激需要所有四种核苷三磷酸的存在,并依赖于外源DNA模板。在没有该因子的情况下,RNA合成在20 - 30分钟后停止,但在有该因子的情况下,合成可持续长达60 - 80分钟。孵育35分钟后添加该因子会导致RNA合成恢复。该因子在低酶浓度下能极大地刺激RNA聚合酶II的活性。当存在该因子时,RNA聚合酶活性对α-鹅膏蕈碱抑制更敏感。[γ-32P]ATP掺入实验表明,该因子能增加RNA链起始的频率,包括初级起始事件以及先前起始事件完成后的重新起始。用该因子也观察到RNA链生长速率略有提高,但通过甲醛/蔗糖梯度离心法测定,合成的RNA的最终大小不受影响。这些数据表明该因子在RNA聚合酶反应的起始阶段起作用。