Blevins Todd
Pikaard Laboratory, Biology Department, Washington University, MO, USA.
Methods Mol Biol. 2010;631:87-107. doi: 10.1007/978-1-60761-646-7_9.
In eukaryotes, RNA silencing encompasses a range of biochemical processes mediated by approximately 20-25 nt small RNAs (smRNAs). This chapter describes northern blot hybridization techniques optimized for detection of such smRNAs, whether extracted from plant or animal tissues. The basic protocol is described, and control blots illustrate the detection specificity and sensitivity of this method using DNA oligonucleotide probes. Known endogenous smRNAs are analyzed in samples prepared from several model plant species, including Arabidopsis thaliana, Nicotiana benthamiana, Oryza sativa, Zea mays, and Physcomitrella patens, as well as the animals Drosophila melanogaster and Mus musculus. Finally, the usefulness of northern blotting in dissecting smRNA biogenesis is shown for the particular case of DNA virus infection.
在真核生物中,RNA沉默涵盖了一系列由大约20 - 25个核苷酸的小RNA(smRNA)介导的生化过程。本章描述了为检测此类smRNA而优化的Northern杂交技术,无论其是从植物还是动物组织中提取的。文中描述了基本方案,对照印迹展示了使用DNA寡核苷酸探针时该方法的检测特异性和灵敏度。在从几种模式植物物种(包括拟南芥、本氏烟草、水稻、玉米和小立碗藓)以及动物果蝇和小家鼠制备的样品中分析了已知的内源性smRNA。最后,针对DNA病毒感染的特定情况,展示了Northern印迹在剖析smRNA生物合成中的实用性。