Ray Debashish, Ha Kevin C H, Nie Kate, Zheng Hong, Hughes Timothy R, Morris Quaid D
Terrence Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario M5S 3E1, Canada.
Department of Molecular Genetics, University of Toronto, Toronto, Ontario M5S 1A8, Canada.
Methods. 2017 Apr 15;118-119:3-15. doi: 10.1016/j.ymeth.2016.12.003. Epub 2016 Dec 10.
RNA-binding proteins (RBPs) participate in diverse cellular processes and have important roles in human development and disease. The human genome, and that of many other eukaryotes, encodes hundreds of RBPs that contain canonical sequence-specific RNA-binding domains (RBDs) as well as numerous other unconventional RNA binding proteins (ucRBPs). ucRBPs physically associate with RNA but lack common RBDs. The degree to which these proteins bind RNA, in a sequence specific manner, is unknown. Here, we provide a detailed description of both the laboratory and data processing methods for RNAcompete, a method we have previously used to analyze the RNA binding preferences of hundreds of RBD-containing RBPs, from diverse eukaryotes. We also determine the RNA-binding preferences for two human ucRBPs, NUDT21 and CNBP, and use this analysis to exemplify the RNAcompete pipeline. The results of our RNAcompete experiments are consistent with independent RNA-binding data for these proteins and demonstrate the utility of RNAcompete for analyzing the growing repertoire of ucRBPs.
RNA结合蛋白(RBPs)参与多种细胞过程,在人类发育和疾病中发挥重要作用。人类基因组以及许多其他真核生物的基因组编码数百种RBPs,其中包含典型的序列特异性RNA结合结构域(RBDs)以及许多其他非常规RNA结合蛋白(ucRBPs)。ucRBPs与RNA发生物理结合,但缺乏常见的RBDs。这些蛋白质以序列特异性方式结合RNA的程度尚不清楚。在这里,我们详细描述了RNAcompete的实验室方法和数据处理方法,RNAcompete是我们之前用于分析来自不同真核生物的数百种含RBD的RBPs的RNA结合偏好的方法。我们还确定了两种人类ucRBPs,即NUDT21和CNBP的RNA结合偏好,并使用此分析来例证RNAcompete流程。我们RNAcompete实验的结果与这些蛋白质的独立RNA结合数据一致,并证明了RNAcompete在分析不断增加的ucRBPs种类方面的实用性。