Meyer S, Nowak K, Sharma V K, Schulze J, Mendel R R, Hänsch R
Institut für Pflanzenbiologie, Technische Universität Braunschweig, Braunschweig, Germany.
Plant Biol (Stuttg). 2004 Jan-Feb;6(1):100-3. doi: 10.1055/s-2004-815729.
The potential of double-stranded RNA interference (RNAi) technology was studied for down-regulation of gene expression in poplar. A set of vectors was constructed generating RNAs capable of duplex formation of sequences specific for the beta-glucuronidase (GUS) reporter gene system. These gene cassettes are driven by the CaMV-35S promoter. To address the question of gene silencing, we tested the functionality of these vectors, both in transient assays by transforming protoplasts with the RNAi constructs, and in stably transformed GUSexpressing poplar plants. Agrobacterium-mediated transformation of those GUS-expressing plants with a GUS-specific RNAi construct showed a strong down-regulation of the reporter gene. From these results we conclude that RNAi is also functional in poplar.
研究了双链RNA干扰(RNAi)技术在杨树中下调基因表达的潜力。构建了一组载体,可产生能够形成针对β-葡萄糖醛酸酶(GUS)报告基因系统特异性序列双链的RNA。这些基因盒由CaMV-35S启动子驱动。为了解决基因沉默问题,我们在通过用RNAi构建体转化原生质体进行的瞬时测定以及稳定转化的表达GUS的杨树植物中测试了这些载体的功能。用GUS特异性RNAi构建体对那些表达GUS的植物进行农杆菌介导的转化,结果显示报告基因强烈下调。从这些结果我们得出结论,RNAi在杨树中也具有功能。