Orii Hidefumi, Mochii Makoto, Watanabe Kenji
Laboratory of Regeneration Biology, Department of Life Science, Graduate School of Science, Himeji Institute of Technology, 3-2-1 Koto, Kamigori, Akou-gun, Hyogo 678-1297, Japan.
Dev Genes Evol. 2003 Apr;213(3):138-41. doi: 10.1007/s00427-003-0310-3. Epub 2003 Mar 12.
A simple method was developed for RNA interference (RNAi) in the planarian Dugesia japonica. The DjIFb ( Dugesia japonica intermediate filament b) gene was used to evaluate the effect of RNAi because both the cDNA and an antiserum against the gene product were available. After transverse cutting at the pre- and post-pharyngeal regions, the middle part of the body fragment was soaked in water containing double-stranded RNA (dsRNA) for about 5 h and then allowed to regenerate in water. On the 5th day of regeneration, little DjIFb protein was detected in the new tissues. When the worms were cut after soaking in dsRNA water, no RNAi effect was observed, suggesting that the dsRNA was introduced through the cut surface. A high concentration of dsRNA or repeated "cutting and soaking" resulted in more effective RNAi. This simple soaking method in combination with expressed sequence tag analysis should be very useful for high-throughput analyses of gene functions in planarian regeneration.
我们开发了一种用于日本三角涡虫RNA干扰(RNAi)的简单方法。使用DjIFb(日本三角涡虫中间丝b)基因来评估RNAi的效果,因为该基因的cDNA和针对基因产物的抗血清均已获得。在咽前和咽后区域进行横切后,将身体片段的中部浸泡在含有双链RNA(dsRNA)的水中约5小时,然后在水中使其再生。在再生的第5天,在新组织中几乎检测不到DjIFb蛋白。当蠕虫在dsRNA水中浸泡后被切断时,未观察到RNAi效应,这表明dsRNA是通过切割表面引入的。高浓度的dsRNA或重复的“切割和浸泡”导致更有效的RNAi。这种简单的浸泡方法与表达序列标签分析相结合,对于涡虫再生中基因功能的高通量分析应该非常有用。