Department of Biology, ETH Zurich (Swiss Federal Institute of Technology), Zurich, Switzerland.
School of Life Sciences, University of Science and Technology of China, Hefei, China.
Methods Mol Biol. 2021;2238:293-312. doi: 10.1007/978-1-0716-1068-8_20.
With a widely established use of quantitative real-time PCR (qRT-PCR) for gene expression analysis, reliable and stable expression of reference genes is often discussed. Suitable reference genes should show less variation of expression across the target samples and allow for error minimization by normalization of qRT-PCR data. Therefore, selection of reliable reference genes is essential for accurate results and to support the conclusions drawn on expression levels of genes under study. In this chapter, we describe the workflow for selection and evaluation of reference genes in rice, including identification of candidate genes by using Genevestigator and evaluation of expression stability using various algorithms. The ranking of the genes guides qRT-PCR performance and data analysis. This protocol used rice as an example but is not limited to rice, and could be applied to other species as well.
随着定量实时 PCR(qRT-PCR)在基因表达分析中的广泛应用,可靠和稳定的参考基因表达经常被讨论。合适的参考基因应该在目标样本中表现出较小的表达变化,并通过 qRT-PCR 数据的归一化来最小化误差。因此,选择可靠的参考基因对于准确的结果和支持对研究基因表达水平的结论是至关重要的。在本章中,我们描述了在水稻中选择和评估参考基因的工作流程,包括使用 Genevestigator 鉴定候选基因和使用各种算法评估表达稳定性。基因的排名指导 qRT-PCR 性能和数据分析。本方案以水稻为例,但不限于水稻,也可应用于其他物种。