Zhang Nannan, Zhang Dandan, Li Jian-Feng
State Key Laboratory of Biocontrol and Guangdong Provincial Key Laboratory of Plant Resources, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Curr Protoc Mol Biol. 2017 Jan 5;117:26.9.1-26.9.10. doi: 10.1002/cpmb.28.
The unpredictability of in planta silencing efficiency of artificial micro RNAs (amiRNAs) has greatly limited the application of the amiRNA technology in basic and applied plant research. This unit describes a simple and robust method called the epitope-tagged protein-based amiRNA (ETPamir) screen for identifying the most effective amiRNA for silencing a particular Arabidopsis gene. After selecting three to four amiRNA candidates designed by the WMD3 web server for the target gene, the silencing efficiencies of the amiRNA candidates can be compared by co-expressing individual amiRNAs with the target mRNA encoding an epitope-tagged target protein in Arabidopsis mesophyll protoplasts. By monitoring target protein levels through immunoblotting with commercial "anti-tag" antibodies, the most potent amiRNA can be easily identified as the one with minimal target protein accumulation. This empirical method bypasses the complexity of amiRNA silencing mechanisms and the scarcity of plant specific antibodies, and can be applied to a broad range of plant species. © 2017 by John Wiley & Sons, Inc.
人工微小RNA(amiRNA)在植物体内沉默效率的不可预测性极大地限制了amiRNA技术在基础植物研究和应用植物研究中的应用。本单元描述了一种简单且可靠的方法,称为基于表位标签蛋白的amiRNA(ETPamir)筛选,用于鉴定沉默特定拟南芥基因的最有效amiRNA。在为目标基因选择由WMD3网络服务器设计的三到四个amiRNA候选物后,通过在拟南芥叶肉原生质体中共同表达单个amiRNA与编码表位标签化目标蛋白的目标mRNA,可以比较amiRNA候选物的沉默效率。通过用商业“抗标签”抗体进行免疫印迹监测目标蛋白水平,可以轻松地将最有效的amiRNA鉴定为目标蛋白积累最少的那个。这种经验方法绕过了amiRNA沉默机制的复杂性和植物特异性抗体的稀缺性,并且可以应用于广泛的植物物种。©2017约翰威立国际出版公司