Seo Jun Sung, Chua Nam-Hai
Laboratory of Plant Molecular Biology, Rockefeller University, New York, NY, USA.
TEMASEK Life Sciences Laboratory, Singapore, Singapore.
Methods Mol Biol. 2019;1933:279-288. doi: 10.1007/978-1-4939-9045-0_17.
Recent advances in next-generation sequencing have revealed that majority of the plant genome is transcribed into long noncoding RNA (lncRNA). Many lncRNAs function by interacting with proteins and forming regulatory complexes. RNA-protein interactions are vital in controlling core cellular processes like transcription and translation. Therefore, identifying proteins that interact with lncRNAs is the first step to deciphering lncRNA functions. Here, we describe an RNA-protein pull-down assay, which enables the identification of proteins that interact with an RNA under study. As an example, we describe pull-down of proteins interacting with lncRNA ELENA1, which promotes the enrichment of MED19a on PR1 promoter to activate PR1 expression.
新一代测序技术的最新进展表明,植物基因组的大部分被转录成长链非编码RNA(lncRNA)。许多lncRNA通过与蛋白质相互作用并形成调控复合物来发挥功能。RNA-蛋白质相互作用在控制转录和翻译等核心细胞过程中至关重要。因此,鉴定与lncRNA相互作用的蛋白质是解读lncRNA功能的第一步。在这里,我们描述了一种RNA-蛋白质下拉实验,该实验能够鉴定与所研究RNA相互作用的蛋白质。作为一个例子,我们描述了与lncRNA ELENA1相互作用的蛋白质的下拉实验,ELENA1可促进MED19a在PR1启动子上的富集以激活PR1表达。