Kane C M, Chamberlin M J
Biochemistry. 1985 Apr 23;24(9):2254-62. doi: 10.1021/bi00330a020.
Transcription by purified mammalian RNA polymerase II in vitro leads to extensive formation of DNA-RNA hybrids between nascent RNA and the template DNA strand. This is especially clear during transcription of 3'-extended (dC-tailed) DNA templates where the nontranscribed DNA strand is progressively displaced as transcription proceeds [Kadesch, T. R., & Chamberlin, M. J. (1982) J. Biol. Chem. 257, 5286-5295]. Addition of small amounts of a HeLa cell extract to such a transcription system enhances renaturation of the template DNA and displacement of the nascent RNA, as measured by the sensitivity of the RNA to pancreatic ribonuclease. Using this latter assay, we have purified a protein factor (renaturase) 250-fold from HeLa cell extracts using chromatography on DEAE-cellulose, DNA-cellulose, and hydroxylapatite. Renaturase preparations facilitate complete renaturation of the template DNA duplex during transcription by RNA polymerase II and lead to concurrent displacement of the nascent RNA. Current preparations are free from all but traces of deoxyribonuclease or ribonuclease. The active component has a molecular weight of about 30000 as estimated by preparative density gradient sedimentation. We have examined the structure of transcribing RNA polymerase II complexes in the presence and absence of renaturase, using the electron microscope and the Williams polylysine technique [Williams, R. C. (1977) Proc. Natl. Acad. Sci. U.S.A. 74, 2311-2315]. In the presence of renaturase, the DNA template is fully renatured, and a ternary complex in which the nascent RNA is displaced during transcription is seen.(ABSTRACT TRUNCATED AT 250 WORDS)
纯化的哺乳动物RNA聚合酶II在体外进行转录时,会在新生RNA与模板DNA链之间广泛形成DNA-RNA杂交体。这在3'-延伸(dC尾)DNA模板的转录过程中尤为明显,随着转录的进行,非转录DNA链会逐渐被取代[卡德施,T.R.,& 钱伯林,M.J.(1982年)《生物化学杂志》257卷,5286 - 5295页]。向这样的转录系统中添加少量的HeLa细胞提取物,可增强模板DNA的复性以及新生RNA的取代,这通过RNA对胰核糖核酸酶的敏感性来衡量。利用后一种检测方法,我们通过在DEAE - 纤维素、DNA - 纤维素和羟基磷灰石上进行层析,从HeLa细胞提取物中纯化出一种蛋白质因子(复性酶)达250倍。复性酶制剂有助于RNA聚合酶II转录过程中模板DNA双链的完全复性,并导致新生RNA同时被取代。目前的制剂除了痕量的脱氧核糖核酸酶或核糖核酸酶外不含其他杂质。通过制备性密度梯度沉降法估计,活性成分的分子量约为30000。我们使用电子显微镜和威廉姆斯聚赖氨酸技术[威廉姆斯,R.C.(1977年)《美国国家科学院院刊》74卷,2311 - 2315页],研究了在有和没有复性酶的情况下转录的RNA聚合酶II复合物的结构。在有复性酶的情况下,DNA模板完全复性,并且可以看到一种三元复合物,其中新生RNA在转录过程中被取代。(摘要截短于250字)