Gilboa E, Soreq H, Aviv H
Eur J Biochem. 1977 Jul 15;77(2):393-400. doi: 10.1111/j.1432-1033.1977.tb11679.x.
Ribonucleotide triphosphates, labeled at the beta position, were synthesized and used directly to quantify RNA chain initiation in nuclei isolated from Friend cells grown in tissue culture. At the optimal salt concentration, low-molecular-weight RNAs (4-5 S) synthesized by RNA polymerase III were the predominant species initiated. Less than 5% of the molecules were initiated by polymerase II. We calculate that 50-80% of the small RNA molecules synthesized in vitro were also initiated in vitro. Assuming that a substantial fraction of the nuclei were active in vitro, the number of 4-5 S RNA molecules initiated per nucleus was about 100 molecules/min.
合成了在β位标记的三磷酸核糖核苷酸,并直接用于定量从组织培养中生长的Friend细胞分离的细胞核中的RNA链起始。在最佳盐浓度下,由RNA聚合酶III合成的低分子量RNA(4 - 5S)是起始的主要种类。由聚合酶II起始的分子不到5%。我们计算出体外合成的小RNA分子中有50 - 80%也是在体外起始的。假设相当一部分细胞核在体外是有活性的,每个细胞核起始的4 - 5S RNA分子数量约为100个分子/分钟。