Guermah Mohamed, Kim Jaehoon, Roeder Robert G
Laboratory of Biochemistry and Molecular Biology, The Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.
Methods. 2009 Aug;48(4):353-60. doi: 10.1016/j.ymeth.2009.02.022. Epub 2009 Mar 9.
In mammalian cells RNA polymerase II efficiently transcribes nucleosome-packaged DNA. In this regard, a fundamental question concerns the nature and mechanism of action of the accessory factors that are necessary and sufficient for, or enhance, transcription through nucleosomal arrays by RNA polymerase II. Here we describe a highly purified system that allows for efficient activator-dependent transcription by RNA polymerase II from the promoter through several contiguous nucleosomes on defined chromatin templates. The system contains natural or recombinant histones, chromatin assembly factors, the histone-acetyltransferase p300, all components of the general transcription machinery, general coactivators and the elongation factor SII (TFIIS). As examples of the applicability of this system for mechanistic analyses of these and other factors, representative experiments show (i) that activated transcription from chromatin templates is concomitantly dependent on the activator, p300-mediated histone acetylation and elongation factor SII/TFIIS. (ii) that SII/TFIIS acts in a highly synergistic manner with p300 (and histone acetylation) at a step subsequent to preinitiation complex (PIC) formation and (iii) that SII/TFIIS works directly at the elongation step of chromatin transcription. Here we describe purification methods for the different factors employed and the specific transcriptional assays that led to the above-mentioned conclusions. This purified system will be very useful as an assay system for the discovery of new factors or the mechanistic analysis of known or candidate factors involved in transcription initiation or elongation on chromatin templates, including factors that effect specific histone modifications or nucleosomal remodeling.
在哺乳动物细胞中,RNA聚合酶II能够有效地转录核小体包装的DNA。在这方面,一个基本问题涉及辅助因子的性质和作用机制,这些辅助因子对于RNA聚合酶II通过核小体阵列进行转录是必要且充分的,或者能够增强转录。在这里,我们描述了一种高度纯化的系统,该系统允许RNA聚合酶II在定义的染色质模板上从启动子通过几个连续的核小体进行高效的激活剂依赖性转录。该系统包含天然或重组组蛋白、染色质组装因子、组蛋白乙酰转移酶p300、通用转录机制的所有组分、通用共激活因子和延伸因子SII(TFIIS)。作为该系统用于这些及其他因子机制分析适用性的示例,代表性实验表明:(i)从染色质模板的激活转录同时依赖于激活剂、p300介导的组蛋白乙酰化和延伸因子SII/TFIIS;(ii)SII/TFIIS在起始前复合物(PIC)形成后的一个步骤中与p300(和组蛋白乙酰化)以高度协同的方式起作用;(iii)SII/TFIIS直接在染色质转录的延伸步骤起作用。在这里,我们描述了所使用的不同因子的纯化方法以及导致上述结论的具体转录测定法。这个纯化系统作为一种检测系统将非常有用,可用于发现新因子或对参与染色质模板上转录起始或延伸的已知或候选因子进行机制分析,包括影响特定组蛋白修饰或核小体重塑的因子。