Department of Biology, Universidad de Santiago de Chile. Av. Libertador Bernardo O'Higgins 3363, Santiago, Chile.
Marine Harvest, camino el Tepual 8, Puerto Montt, Chile.
Sci Rep. 2017 May 11;7(1):1756. doi: 10.1038/s41598-017-01970-3.
MicroRNAs are key non-coding RNA molecules that play a relevant role in the regulation of gene expression through translational repression and/or transcript cleavage during normal development and physiological adaptation processes like stress. Quantitative reverse transcription polymerase chain reaction (RT-qPCR) has become the approach normally used to determine the levels of microRNAs. However, this approach needs the use of endogenous reference. An improper selection of endogenous references can result in confusing interpretation of data. The aim of this study was to identify and validate appropriate endogenous reference miRNA genes for normalizing RT-qPCR survey of miRNAs expression in four different tissues of Atlantic salmon, under handling and confinement stress conditions associated to early or primary stress response. Nine candidate reference normalizers, including microRNAs and nuclear genes, normally used in vertebrate microRNA expression studies were selected from literature, validated by RT-qPCR and analyzed by the algorithms geNorm and NormFinder. The results revealed that the ssa-miR-99-5p gene was the most stable overall and that ssa-miR-99-5p and ssa-miR-23a-5p genes were the best combination. Moreover, the suitability of ssa-miR-99-5p and ssa-miR-23a-5p as endogeneuos reference genes was demostrated by the expression analysis of ssa-miR-193-5p gene.
MicroRNAs 是关键的非编码 RNA 分子,它们在正常发育和生理适应过程(如应激)中通过翻译抑制和/或转录切割来调节基因表达,发挥着重要作用。定量逆转录聚合酶链反应(RT-qPCR)已成为确定 microRNAs 水平的常用方法。然而,这种方法需要使用内源性参照。内源性参照选择不当可能导致数据解释混乱。本研究的目的是鉴定和验证大西洋鲑鱼四种不同组织中 microRNAs 表达的 RT-qPCR 调查的合适内源性参照 microRNA 基因,这些组织在与早期或初级应激反应相关的处理和限制应激条件下。从文献中选择了 9 个候选参考正常化器,包括 microRNAs 和脊椎动物 microRNA 表达研究中常用的核基因,通过 RT-qPCR 进行验证,并通过 geNorm 和 NormFinder 算法进行分析。结果表明,ssa-miR-99-5p 基因总体上最稳定,ssa-miR-99-5p 和 ssa-miR-23a-5p 基因是最佳组合。此外,通过 ssa-miR-193-5p 基因的表达分析证明了 ssa-miR-99-5p 和 ssa-miR-23a-5p 作为内源性参考基因的适用性。