State Key Laboratory for Ecological Pest Control of Fujian and Taiwan Crops, Institute of Applied Ecology, Fujian Agriculture and Forestry University, Fuzhou, China.
International Joint Research Laboratory of Ecological Pest Control, Ministry of Education, Fujian Agriculture and Forestry University, Fuzhou, China.
PLoS One. 2019 Aug 1;14(8):e0220475. doi: 10.1371/journal.pone.0220475. eCollection 2019.
The establishment of an expression quantification system that can be easily applied for the comparison of microRNAs (miRNAs) from biological samples is an important step toward understanding functional mechanisms in organisms. However, there is lack of attention on the selection of reference genes for miRNA expression profiling in insect herbivores. Here, we explored the candidate reference genes in a notorious pest of cruciferous crops, Plutella xylostella, for normalization of miRNA expression in developmental stages and tissues and in response to a change of food source from artificial diet to host plant Arabidopsis thaliana. We first compared the expression levels and stability of eight small RNAs using qRT-PCR, and found that miR11 was the most suitable reference gene for expression quantification of the miRNAs. We then confirmed this finding using digital droplet PCR and further validated with a well-studied cross-kingdom miRNA derived from A. thaliana (ath-miR159a). However, none of the reference genes was applicable for all experimental conditions, and multiple reference genes were sometimes required within the same experiment. Our work provides a method for the selection of reference genes for quantification of plant-derived miRNAs, which paves the way for unveiling their roles in the insect-plant coevolution.
建立一个易于应用于比较生物样本中 microRNAs(miRNAs)的表达定量系统,是理解生物体功能机制的重要步骤。然而,对于昆虫草食者中 miRNA 表达谱分析的参考基因选择,却缺乏关注。在这里,我们探索了十字花科作物中一种臭名昭著的害虫小菜蛾(Plutella xylostella)的候选参考基因,用于在发育阶段和组织中以及在食物来源从人工饲料转变为宿主植物拟南芥(Arabidopsis thaliana)时,对 miRNA 表达进行归一化。我们首先使用 qRT-PCR 比较了 8 种小 RNA 的表达水平和稳定性,发现 miR11 是最适合用于 miRNA 表达定量的参考基因。我们然后使用数字液滴 PCR 进一步验证了这一发现,并使用源自拟南芥的研究充分的跨领域 miRNA(ath-miR159a)进行了验证。然而,没有一个参考基因适用于所有实验条件,并且在同一个实验中有时需要多个参考基因。我们的工作为植物源性 miRNA 定量的参考基因选择提供了一种方法,为揭示它们在昆虫-植物共同进化中的作用铺平了道路。