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Normalization with genes encoding ribosomal proteins but not GAPDH provides an accurate quantification of gene expressions in neuronal differentiation of PC12 cells

机译:用编码核糖体蛋白而不是GAPDH的基因进行归一化可以准确定量PC12细胞神经元分化中的基因表达

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摘要

BackgroundGene regulation at transcript level can provide a good indication of the complex signaling mechanisms underlying physiological and pathological processes. Transcriptomic methods such as microarray and quantitative real-time PCR require stable reference genes for accurate normalization of gene expression. Some but not all studies have shown that housekeeping genes (HGKs), β-actin (ACTB) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which are routinely used for normalization, may vary significantly depending on the cell/tissue type and experimental conditions. It is currently unclear if these genes are stably expressed in cells undergoing drastic morphological changes during neuronal differentiation. Recent meta-analysis of microarray datasets showed that some but not all of the ribosomal protein genes are stably expressed. To test the hypothesis that some ribosomal protein genes can serve as reference genes for neuronal differentiation, a genome-wide analysis was performed and putative reference genes were identified based on stability of expressions. The stabilities of these potential reference genes were then analyzed by reverse transcription quantitative real-time PCR in six differentiation conditions.
机译:转录水平上的BackgroundGene调控可以很好地说明生理和病理过程背后的复杂信号传导机制。转录组学方法(例如微阵列和定量实时PCR)需要稳定的参考基因,以实现基因表达的准确标准化。一些但并非全部研究表明,通常用于标准化的管家基因(HGK),β-肌动蛋白(ACTB)和甘油三磷酸脱氢酶(GAPDH)可能会因细胞/组织类型和实验而有很大差异条件。目前尚不清楚这些基因是否在神经元分化过程中经历剧烈形态变化的细胞中稳定表达。最近对微阵列数据集的荟萃分析表明,一些但不是全部的核糖体蛋白基因稳定表达。为了检验某些核糖体蛋白基因可以作为神经元分化参考基因的假设,进行了全基因组分析,并根据表达的稳定性鉴定了假定的参考基因。这些潜在的参考基因的稳定性,然后通过逆转录定量实时PCR在六个分化条件下进行了分析。

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