Ahmed Farid E, Gouda Mostafa M, Hussein Laila A, Ahmed Nancy C, Vos Paul W, Mohammad Mahmoud A
GEM Tox Labs, Institute for Research in Biotechnology, Greenville, NC, U.S.A.
Department of Nutrition & Food Science, National Research Centre, Dokki, Cairo, Egypt.
Cancer Genomics Proteomics. 2017 Nov-Dec;14(6):469-481. doi: 10.21873/cgp.20057.
This article illustrates the importance of melt curve analysis (MCA) in interpretation of mild nutrogenomic micro(mi)RNA expression data, by measuring the magnitude of the expression of key miRNA molecules in stool of healthy human adults as molecular markers, following the intake of Pomegranate juice (PGJ), functional fermented sobya (FS), rich in potential probiotic lactobacilli, or their combination. Total small RNA was isolated from stool of 25 volunteers before and following a three-week dietary intervention trial. Expression of 88 miRNA genes was evaluated using Qiagen's 96 well plate RT miRNA qPCR arrays. Employing parallel coordinates plots, there was no observed significant separation for the gene expression (Cq) values, using Roche 480® PCR LightCycler instrument used in this study, and none of the miRNAs showed significant statistical expression after controlling for the false discovery rate. On the other hand, melting temperature profiles produced during PCR amplification run, found seven significant genes (miR-184, miR-203, miR-373, miR-124, miR-96, miR-373 and miR-301a), which separated candidate miRNAs that could function as novel molecular markers of relevance to oxidative stress and immunoglobulin function, for the intake of polyphenol (PP)-rich, functional fermented foods rich in lactobacilli (FS), or their combination. We elaborate on these data, and present a detailed review on use of melt curves for analyzing nutigenomic miRNA expression data, which initially appear to show no significant expressions, but are actually more subtle than this simplistic view, necessitating the understanding of the role of MCA for a comprehensive understanding of what the collective expression and MCA data collectively imply.
本文通过测量健康成年人类粪便中关键微小RNA(miRNA)分子的表达量作为分子标志物,阐述了熔解曲线分析(MCA)在解读轻度营养基因组微小RNA(mi)表达数据中的重要性。研究对象为摄入石榴汁(PGJ)、富含潜在益生菌乳酸菌的功能性发酵大豆(FS)或二者组合后的个体。在为期三周的饮食干预试验前后,从25名志愿者的粪便中分离出总小RNA。使用Qiagen的96孔板RT miRNA qPCR阵列评估88个miRNA基因的表达。利用平行坐标图,使用本研究中所用的罗氏480®PCR LightCycler仪器,未观察到基因表达(Cq)值有显著分离,并且在控制错误发现率后,没有miRNA显示出显著的统计学表达。另一方面,在PCR扩增过程中产生的熔解温度曲线发现了7个显著基因(miR - 184、miR - 203、miR - 373、miR - 124、miR - 96、miR - 373和miR - 301a),这些基因分离出了可能作为与氧化应激和免疫球蛋白功能相关的新型分子标志物的候选miRNA,用于摄入富含多酚(PP)的、富含乳酸菌的功能性发酵食品(FS)或二者组合的情况。我们详细阐述了这些数据,并对使用熔解曲线分析营养基因组miRNA表达数据进行了详细综述,这些数据最初似乎没有显著表达,但实际上比这种简单的观点更为微妙,因此有必要理解MCA的作用,以便全面理解集体表达和MCA数据共同所暗示的内容。