Arribas-Hernández Laura, Vigh Maria Louisa, Brodersen Peter
Department of Biology, University of Copenhagen, Ole Maaløes Vej 5, Copenhagen, DK-2200, Copenhagen N, Denmark.
Methods Mol Biol. 2019;1932:295-316. doi: 10.1007/978-1-4939-9042-9_22.
Small RNA-guided endonucleolysis ("slicing") of target mRNA is the signature biochemical activity underlying many RNA silencing phenomena. The catalytic slicer activity resides in Argonaute (AGO) proteins. Here, we present two protocols to detect microRNA-guided slicer activity of AGO1 immunopurified from Arabidopsis tissues. The first uses radioactive, cap-labeled RNA substrates produced by in vitro transcription of RNA fragments corresponding to endogenous target sites flanked by 100-200 nucleotides of target sequence. The second protocol uses similarly designed but shorter (around 50 nt) fluorescently labeled RNA. Advantages and disadvantages of the two setups are also discussed.
小RNA引导的靶标mRNA内切核酸酶活性(“切割”)是许多RNA沉默现象背后的标志性生化活性。催化切割活性存在于AGO(Argonaute)蛋白中。在此,我们提供了两种方法来检测从拟南芥组织中免疫纯化的AGO1的微小RNA引导的切割活性。第一种方法使用放射性、帽标记的RNA底物,这些底物是通过体外转录与内源靶位点对应的RNA片段产生的,该片段两侧为100 - 200个核苷酸的靶序列。第二种方法使用设计类似但较短(约50 nt)的荧光标记RNA。我们还讨论了这两种方法的优缺点。