Conrad Nicholas K
Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Methods Enzymol. 2008;449:317-42. doi: 10.1016/S0076-6879(08)02415-4.
From the moment a nascent transcript emerges from an RNA polymerase until its ultimate destruction, an RNA is bound by proteins that govern its fate. Thus, in order to understand posttranscriptional regulation of gene expression, it is essential to ascertain which proteins bind a given RNA in vivo. This chapter describes three immunoprecipitation-based assays designed to query the in vivo makeup of RNA-protein complexes. Two of these, UV cross-linking and RNA immunoprecipitation (RIP), include cross-linking steps that trap complexes formed in vivo. A third, a cell mixing experiment, verifies that an interaction occurs in vivo by controlling for RNA-protein association subsequent to cell lysis. Using these protocols, this chapter presents evidence that the abundant nuclear RNA-binding protein hnRNP C interacts with the Kaposi's sarcoma-associated herpesvirus polyadenylated nuclear RNA in vivo.
从新生转录本从RNA聚合酶中出现的那一刻起,直到其最终被降解,RNA都与决定其命运的蛋白质结合。因此,为了理解基因表达的转录后调控,确定哪些蛋白质在体内与特定的RNA结合至关重要。本章描述了三种基于免疫沉淀的实验方法,旨在探究RNA-蛋白质复合物在体内的组成。其中两种方法,紫外线交联和RNA免疫沉淀(RIP),包括交联步骤,可捕获体内形成的复合物。第三种方法,细胞混合实验,通过控制细胞裂解后RNA-蛋白质的结合来验证体内是否发生相互作用。利用这些实验方案,本章提供了证据,证明丰富的核RNA结合蛋白hnRNP C在体内与卡波西肉瘤相关疱疹病毒多聚腺苷酸化核RNA相互作用。