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通过 RNA 测序分析预测鳞翅目昆虫中有效的 RNA 干扰靶标和通路相关基因。

Prediction of effective RNA interference targets and pathway-related genes in lepidopteran insects by RNA sequencing analysis.

机构信息

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.

出版信息

Insect Sci. 2018 Jun;25(3):356-367. doi: 10.1111/1744-7917.12437. Epub 2017 Apr 10.

Abstract

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.

摘要

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。

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