Bartsch Deniz, Zirkel Anne, Kurian Leo
Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases, University of Cologne, Cologne, Germany.
Institute for Neurophysiology, University of Cologne, Cologne, Germany.
Methods Mol Biol. 2018;1724:159-166. doi: 10.1007/978-1-4939-7562-4_13.
A substantial proportion of the currently annotated genes in eukaryotes are proposed to function as RNA molecules (>200 bp) with no significant protein coding potential, currently classified as long noncoding RNAs (lncRNA). A distinct subgroup of lncRNAs is circular RNAs (circRNAs), which can be easily identified by unique junction reads, resulting from their biogenesis. CircRNAs are largely cytosolic and thought to either code for micro-peptides or facilitate gene regulation by sequestering microRNAs (miRNAs) or RNA-binding proteins (RBPs) from their targets. Interrogation of the interaction of circRNAs with cellular macromolecular machineries could indicate their mode of action. Here, we detail a sucrose gradient-based method to pinpoint association of a given circRNA (or any transcript of interest) with distinct ribosomal fractions. This method can evaluate the coding potential of candidate circRNAs (or any transcript of interest) and its association with the translation machinery.
真核生物中目前注释的基因有很大一部分被认为作为RNA分子(>200bp)发挥作用,没有明显的蛋白质编码潜力,目前被归类为长链非编码RNA(lncRNA)。lncRNA的一个独特亚组是环状RNA(circRNA),由于其生物发生过程,可通过独特的连接读数轻松识别。circRNA主要存在于细胞质中,被认为要么编码微肽,要么通过从其靶标中隔离微小RNA(miRNA)或RNA结合蛋白(RBP)来促进基因调控。研究circRNA与细胞大分子机制的相互作用可以揭示它们的作用模式。在这里,我们详细介绍一种基于蔗糖梯度的方法,以确定给定的circRNA(或任何感兴趣的转录本)与不同核糖体组分的关联。该方法可以评估候选circRNA(或任何感兴趣的转录本)的编码潜力及其与翻译机制的关联。