Song Hui, Zhang Xiao, Shi Cong, Wang Shuangshuang, Wu Ailin, Wei Chaoling
State Key Laboratory of Tea Plant Biology and Utilization, Anhui Agricultural University, 130 Changjiang West Road, Hefei 230036, China.
Genes (Basel). 2016 May 28;7(6):25. doi: 10.3390/genes7060025.
Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) is a rapid and sensitive method for analyzing microRNA (miRNA) expression. However, accurate qRT-PCR results depend on the selection of reliable reference genes as internal positive controls. To date, few studies have identified reliable reference genes for differential expression analysis of miRNAs among tissues, and among experimental conditions in plants. In this study, three miRNAs and four non-coding small RNAs (ncRNA) were selected as reference candidates, and the stability of their expression was evaluated among different tissues and under different experimental conditions in the tea plant (Camellia sinensis) using the geNorm and NormFinder programs. It was shown that miR159a was the best single reference gene in the bud to the fifth leaf, 5S rRNA was the most suitable gene in different organs, miR6149 was the most stable gene when the leaves were attacked by Ectropis oblique and U4, miR5368n and miR159a were the best genes when the leaves were treated by methyl jasmonate (MeJA), salicylic acid (SA) and abscisic acid (ABA), respectively. Our results provide suitable reference genes for future investigations on miRNA functions in tea plants.
定量逆转录-聚合酶链反应(qRT-PCR)是一种用于分析微小RNA(miRNA)表达的快速且灵敏的方法。然而,准确的qRT-PCR结果取决于选择可靠的内参基因作为内部阳性对照。迄今为止,很少有研究确定用于植物组织间以及实验条件下miRNA差异表达分析的可靠内参基因。在本研究中,选择了三种miRNA和四种非编码小RNA(ncRNA)作为候选内参,使用geNorm和NormFinder程序评估了它们在茶树(Camellia sinensis)不同组织间以及不同实验条件下的表达稳定性。结果表明,miR159a是芽到第五片叶中最佳的单一内参基因,5S rRNA是不同器官中最合适的基因,miR6149是叶片受到茶尺蠖攻击时最稳定的基因,而U4、miR5368n和miR159a分别是叶片用茉莉酸甲酯(MeJA)、水杨酸(SA)和脱落酸(ABA)处理时的最佳基因。我们的结果为今后茶树miRNA功能研究提供了合适的内参基因。