Park Jung-Eun, Lee Kyong Yun, Lee Se-Jin, Oh Wan-Suk, Jeong Pan-Young, Woo Taeha, Kim Chang-Bae, Paik Young-Ki, Koo Hyeon-Sook
Department of Biochemistry, College of Science, Yonsei University, Seoul 120-749, Korea.
Mol Cells. 2008 Jul 31;26(1):81-6. Epub 2008 Jun 4.
RNA interference (RNAi) was performed on several essential genes in the pinewood nematode Bursaphelenchus xylophilus, which causes pine wilt disease. Double-stranded RNA (dsRNA) was delivered to larvae or adult worms by soaking, electroporation, or microinjection. Soaking and electroporation of L2-L3 stage worms in solutions containing dsRNA for essential genes induced over 25% lethality after 5 days, and gene-specific phenotypes were observed. This lethality agreed with significant reductions of the targeted transcripts, as assayed by reverse-transcription coupled with real time PCR. Microinjection was the most efficient route as measured by the hatching rate of F1 embryos, which was reduced by 46%. When adult worms were soaked in dsRNA, lethality was induced in the F1 larvae, revealing the persistence of knockdown phenotypes. The penetrance of the RNAi phenotypes for essential genes was relatively low but consistent, indicating that RNAi should be useful for studying the in vivo functions of B. xylophilus gene products.
RNA干扰(RNAi)技术被应用于松材线虫(Bursaphelenchus xylophilus)的几个关键基因上,松材线虫会引发松树枯萎病。双链RNA(dsRNA)通过浸泡、电穿孔或显微注射的方式递送至幼虫或成虫体内。将处于L2-L3阶段的线虫浸泡或进行电穿孔处理,使其处于含有关键基因dsRNA的溶液中,5天后诱导出超过25%的致死率,并观察到了基因特异性表型。通过逆转录结合实时PCR检测发现,这种致死率与靶向转录本的显著减少相一致。以F1胚胎的孵化率衡量,显微注射是最有效的途径,F1胚胎孵化率降低了46%。当成虫浸泡在dsRNA中时,F1幼虫出现致死现象,这表明基因敲低表型具有持续性。关键基因的RNAi表型的外显率相对较低但较为稳定,这表明RNAi技术对于研究松材线虫基因产物的体内功能应该是有用的。