Wong Terrence N, Pan Tao
Department of Biochemistry & Molecular Biology, University of Chicago, Chicago, Illinois, USA.
Methods Enzymol. 2009;468:167-93. doi: 10.1016/S0076-6879(09)68009-5.
RNA folds during transcription in the cell. Compared to most in vitro studies where the focus is generally on Mg(2+)-initiated refolding of fully synthesized transcripts, cotranscriptional RNA folding studies better replicate how RNA folds in a cellular environment. Unique aspects of cotranscriptional folding include the 5'- to 3'-polarity of RNA, the transcriptional speed, pausing properties of the RNA polymerase, the effect of the transcriptional complex and associated factors, and the effect of RNA-binding proteins. Identifying strategic pause sites can reveal insights on the folding pathway of the nascent transcript. Structural mapping of the paused transcription complexes identifies important folding intermediates along these pathways. Oligohybridization assays and the appearance of the catalytic activity of a ribozyme either in trans or in cis can be used to monitor cotranscriptional folding under a wide range of conditions. In our laboratory, these methodologies have been applied to study the folding of three highly conserved RNAs (RNase P, SRP, and tmRNA), several circularly permuted forms of a bacterial RNase P RNA, a riboswitch (thiM), and an aptamer-activated ribozyme (glmS).
RNA在细胞内转录过程中发生折叠。与大多数体外研究不同,体外研究通常聚焦于完全合成的转录本由Mg(2+)引发的重折叠,而共转录RNA折叠研究能更好地重现RNA在细胞环境中的折叠方式。共转录折叠的独特之处包括RNA的5'至3'极性、转录速度、RNA聚合酶的暂停特性、转录复合物及相关因子的作用,以及RNA结合蛋白的作用。识别关键暂停位点可揭示新生转录本折叠途径的相关信息。对暂停转录复合物的结构图谱分析可确定这些途径上重要的折叠中间体。寡核苷酸杂交分析以及核酶反式或顺式催化活性的出现可用于在多种条件下监测共转录折叠。在我们实验室,这些方法已被用于研究三种高度保守的RNA(核糖核酸酶P、信号识别颗粒和转移信使RNA)、细菌核糖核酸酶P RNA的几种环形排列形式、一种核糖开关(硫胺素M)以及一种适体激活核酶(谷氨酰胺合成酶)的折叠。