Izban M G, Luse D S
Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati College of Medicine, Ohio 45267-0524.
J Biol Chem. 1992 Jul 5;267(19):13647-55.
We used an in vitro assay system based on HeLa cell core transcription components to examine transcript elongation by RNA polymerase II on either naked DNA or chromatin templates as a function of the three known elongation factors, IIS, TFIIF, and TFIIX. We demonstrate for the first time that mammalian RNA polymerase II can achieve physiological elongation rates on naked DNA templates in vitro. The addition of TFIIF alone gave this rate, although IIS was required to minimize the block to elongation at intrinsic termination sites. However, IIS and TFIIF provided only a slight increase in the very poor elongation efficiency of RNA polymerase II on chromatin templates. The addition of TFIIX to reactions containing IIS and TFIIF reduced the elongation rate on naked DNA templates but slightly increased the elongation efficiency on chromatin. The ability of elongation factors either separately or in combination to stimulate transcription on naked DNA and chromatin templates was also examined.
我们使用了基于HeLa细胞核转录组件的体外分析系统,以研究RNA聚合酶II在裸露DNA或染色质模板上的转录延伸情况,该延伸作为三种已知延伸因子IIS、TFIIF和TFIIX的函数。我们首次证明,哺乳动物RNA聚合酶II在体外裸露DNA模板上能够达到生理延伸速率。单独添加TFIIF即可实现此速率,尽管需要IIS来最小化内在终止位点对延伸的阻碍。然而,IIS和TFIIF仅略微提高了RNA聚合酶II在染色质模板上极低的延伸效率。在含有IIS和TFIIF的反应中添加TFIIX会降低在裸露DNA模板上的延伸速率,但略微提高在染色质上的延伸效率。我们还研究了延伸因子单独或组合刺激在裸露DNA和染色质模板上转录的能力。