The William Harvey Research Institute, Barts and The London School of Medicine, Queen Mary University of London, Charterhouse Square, London, EC1M 6BQ, UK,
Inflammation. 2014 Aug;37(4):1059-69. doi: 10.1007/s10753-014-9829-x.
Gene expression studies are fundamental for the understanding of complex diseases, providing new insights into the pathogenic process and new tools for diagnostic and patient stratification. Gene profiling studies by real-time PCR require the use of reference genes for normalization and an appropriate validation is essential for accurate results. We performed a comprehensive assessment of six common housekeeping genes in the K/BxN serum-induced arthritis model in mice. Classical statistics and NormFinder analyses pointed out Gapdh as the less stable and therefore unsuitable as a reference control. Gapdh was considerably down-regulated in arthritic joints and therefore produced an overestimation of transcriptional changes. Hptr, B2m, and Rpl13a showed the most constant expression. Collectively our data advise against the use of Gapdh in gene expression studies in the acute phase of the K/BxN model and adds a cautionary note on the need to validate the reference genes for reliable, comparable, and reproducible results.
基因表达研究对于理解复杂疾病至关重要,为发病机制提供了新的见解,并为诊断和患者分层提供了新的工具。实时 PCR 的基因谱研究需要使用参考基因进行归一化,准确的结果需要进行适当的验证。我们在 K/BxN 血清诱导的关节炎小鼠模型中对六种常见管家基因进行了全面评估。经典统计学和 NormFinder 分析指出 Gapdh 是最不稳定的,因此不适合作为参考对照。关节炎关节中的 Gapdh 明显下调,因此会高估转录变化。Hptr、B2m 和 Rpl13a 表现出最稳定的表达。我们的数据共同表明,在 K/BxN 模型的急性期基因表达研究中不应该使用 Gapdh,并提醒需要验证参考基因以获得可靠、可比和可重复的结果。