Blevins Todd
Institut de Biologie Moléculaire des Plantes, Centre National de la Recherche Scientifique (CNRS) UPR2357, 12 rue du Général Zimmer, Strasbourg Cedex, 67084, USA.
Methods Mol Biol. 2017;1456:141-162. doi: 10.1007/978-1-4899-7708-3_12.
Cells have evolved intricate RNA-directed mechanisms that destroy viruses, silence transposons, and regulate gene expression. These nucleic acid surveillance and gene silencing mechanisms rely upon the selective base-pairing of ~19-25 nt small RNAs to complementary RNA targets. This chapter describes northern blot hybridization techniques for the detection of such small RNAs. Blots spiked with synthetic standards are used to illustrate the detection specificity and sensitivity of DNA oligonucleotide probes. Known endogenous small RNAs are then analyzed in samples prepared from several model plants, including Arabidopsis thaliana, Nicotiana benthamiana, Oryza sativa, Zea mays, and Physcomitrella patens, as well as from the animals Drosophila melanogaster and Mus musculus. Finally, the value of northern blotting for dissecting small RNA biogenesis is shown using an example of virus infection in A. thaliana.
细胞进化出了复杂的RNA导向机制,这些机制可破坏病毒、沉默转座子并调控基因表达。这些核酸监测和基因沉默机制依赖于约19 - 25个核苷酸的小RNA与互补RNA靶标的选择性碱基配对。本章描述了用于检测此类小RNA的Northern印迹杂交技术。用合成标准品加标的印迹用于说明DNA寡核苷酸探针的检测特异性和灵敏度。然后在从几种模式植物制备的样品中分析已知的内源性小RNA,这些植物包括拟南芥、本氏烟草、水稻、玉米和小立碗藓,以及动物黑腹果蝇和小家鼠。最后,以拟南芥中的病毒感染为例,展示了Northern印迹在剖析小RNA生物合成方面的价值。