Conaway R C, Reines D, Garrett K P, Powell W, Conaway J W
Program in Molecular and Cell Biology, Oklahoma Medical Research Foundation, Oklahoma City 73104, USA.
Methods Enzymol. 1996;273:194-207. doi: 10.1016/s0076-6879(96)73020-3.
Eukaryotic messenger RNA synthesis is a complex biochemical process requiring the concerted action of multiple “general” transcription factors (TFs) that control the activity of RNA polymerase II at both the initiation and elongation stages of transcription. Because the general transcription factors are present at low levels in mammalian cells, their purification is a formidable undertaking. For this reason we explored the feasibility of using rat liver as a source for purification of the general factors. Rat liver has proven to be an ideal model system for biochemical studies of transcription initiation and elongation by RNA polymerase II (Figs. 1 and 2). In our hands the yield of general transcription factors per gram of rat liver is roughly equivalent to their yield per gram of cultured HeLa cells. Moreover, we have been able to develop convenient and reproducible methods for preparation of rat liver extracts from as much as 1 kg of liver per day. Because it is both technically difficult and expensive to obtain such quantities of cultured cells on a daily basis, rat liver provides a significant logistic advantage for purification of the general transcription factors.
真核生物信使核糖核酸(mRNA)的合成是一个复杂的生化过程,需要多种“通用”转录因子(TFs)协同作用,这些转录因子在转录的起始和延伸阶段控制RNA聚合酶II的活性。由于通用转录因子在哺乳动物细胞中的含量很低,对其进行纯化是一项艰巨的任务。因此,我们探索了以大鼠肝脏作为纯化通用因子来源的可行性。事实证明,大鼠肝脏是研究RNA聚合酶II转录起始和延伸生化过程的理想模型系统(图1和图2)。在我们的实验中,每克大鼠肝脏中通用转录因子的产量大致相当于每克培养的HeLa细胞中的产量。此外,我们已经能够开发出方便且可重复的方法,每天从多达1千克的肝脏中制备大鼠肝脏提取物。由于每天获取如此大量的培养细胞在技术上既困难又昂贵,大鼠肝脏为纯化通用转录因子提供了显著的后勤优势。