Key Laboratory of Insect Developmental and Evolutionary Biology, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China.
Insect Sci. 2018 Jun;25(3):356-367. doi: 10.1111/1744-7917.12437. Epub 2017 Apr 10.
When using RNA interference (RNAi) to study gene functions in Lepidoptera insects, we discovered that some genes could not be suppressed; instead, their expression levels could be up-regulated by double-stranded RNA (dsRNA). To predict which genes could be easily silenced, we treated the Asian corn borer (Ostrinia furnacalis) with dsGFP (green fluorescent protein) and dsMLP (muscle lim protein). A transcriptome sequence analysis was conducted using the cDNAs 6 h after treatment with dsRNA. The results indicated that 160 genes were up-regulated and 44 genes were down-regulated by the two dsRNAs. Then, 50 co-up-regulated, 25 co-down-regulated and 43 unaffected genes were selected to determine their RNAi responses. All the 25 down-regulated genes were knocked down by their corresponding dsRNA. However, several of the up-regulated and unaffected genes were up-regulated when treated with their corresponding dsRNAs instead of being knocked down. The genes up-regulated by the dsGFP treatment may be involved in insect immune responses or the RNAi pathway. When the immune-related genes were excluded, only seven genes were induced by dsGFP, including ago-2 and dicer-2. These results not only provide a reference for efficient RNAi target predications, but also provide some potential RNAi pathway-related genes for further study.
当使用 RNA 干扰(RNAi)来研究鳞翅目昆虫的基因功能时,我们发现有些基因不能被抑制;相反,双链 RNA(dsRNA)可以上调它们的表达水平。为了预测哪些基因容易被沉默,我们用 dsGFP(绿色荧光蛋白)和 dsMLP(肌肉 lim 蛋白)处理亚洲玉米螟(Ostrinia furnacalis)。在 dsRNA 处理 6 小时后,使用 cDNA 进行转录组序列分析。结果表明,两种 dsRNA 分别上调了 160 个基因,下调了 44 个基因。然后,选择了 50 个共上调、25 个共下调和 43 个不受影响的基因来确定它们的 RNAi 反应。所有 25 个下调的基因都被相应的 dsRNA 敲低了。然而,一些上调和不受影响的基因在用相应的 dsRNA 处理时被上调,而不是被敲低。dsGFP 处理上调的基因可能参与昆虫免疫反应或 RNAi 途径。当排除与免疫相关的基因后,dsGFP 仅诱导了七个基因,包括 ago-2 和 dicer-2。这些结果不仅为高效的 RNAi 靶标预测提供了参考,还为进一步研究提供了一些潜在的 RNAi 途径相关基因。