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Selection of Reference Genes for MicroRNA Quantitative Expression Analysis in Chinese Perch, Siniperca chuatsi

机译:中国鲈鱼MicroRNA定量表达分析参考基因的选择

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Real-time quantitative reverse transcription PCR (RT-qPCR) is one of the most effective and sensitive techniques in gene expression assay, for which selection of reference genes is a prerequisite. In teleost species, such as Chinese perch, the expression profiling of miRNAs as reference genes for RT-qPCR has not been intensively studied. In the present study, the expression profiles of six miRNAs (miR-101a, miR-146a, miR-22a, miR-23a, miR-26a and let-7a) and one small nuclear RNA (U6) were assayed with RT-qPCR in different adult tissues, developmental stages and growth conditions of Chinese perch, Siniperca chuatsi. The analyses revealed that embryonic developmental stage is an important variability factor in the expression stability of miRNAs. All six miRNAs exhibited better expression consistency than U6 in most of the conditions examined, and therefore, they may be more suitable as a reference gene for miRNA quantification. When different tissues and developmental stages were considered, miR-22a demonstrated the most consistent expression pattern, and the best combination of reference genes was miR-22a and miR-23a. Our study offers useful data for selecting miRNAs as reference genes for RT-qPCR analysis of miRNAs in teleost fishes under different conditions.
机译:实时定量逆转录PCR(RT-qPCR)是基因表达测定中最有效,最灵敏的技术之一,因此选择参考基因是前提。在硬骨鱼类中,例如中国鲈,尚未深入研究作为RT-qPCR参考基因的miRNA的表达谱。在本研究中,使用RT-qPCR检测了6个miRNA(miR-101a,miR-146a,miR-22a,miR-23a,miR-26a和let-7a)和一个小核RNA(U6)的表达谱。中华鲈(Siniperca chuatsi)在不同的成年组织,发育阶段和生长条件分析表明,胚胎发育阶段是miRNAs表达稳定性的重要变异因子。在所检查的大多数条件下,所有六个miRNA均表现出比U6更好的表达一致性,因此,它们可能更适合作为miRNA定量的参考基因。当考虑不同的组织和发育阶段时,miR-22a表现出最一致的表达模式,而参考基因的最佳组合是miR-22a和miR-23a。我们的研究提供了有用的数据,可用于选择miRNA作为参考基因,用于在不同条件下硬骨鱼中miRNA的RT-qPCR分析。

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