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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准确定量PC12细胞神经元分化中的基因表达

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Background Gene 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. Results Twenty stably expressed genes, including thirteen ribosomal protein genes, were selected from microarray analysis of the gene expression profiles of GDNF and NGF induced differentiation of PC12 cells. The expression levels of these candidate genes as well as ACTB and GAPDH were further analyzed by reverse transcription quantitative real-time PCR in PC12 cells differentiated with a variety of stimuli including NGF, GDNF, Forskolin, KCl and ROCK inhibitor, Y27632. The performances of these candidate genes as stable reference genes were evaluated with two independent statistical approaches, geNorm and NormFinder. Conclusions The ribosomal protein genes, RPL19 and RPL29, were identified as suitable reference genes during neuronal differentiation of PC12 cells, regardless of the type of differentiation conditions. The combination of these two novel reference genes, but not the commonly used HKG, GAPDH, allows robust and accurate normalization of differentially expressed genes during PC12 differentiation.
机译:转录本水平的背景基因调节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归一化。一些但并非全部研究表明,通常用于归一化的管家基因(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,某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。然后通过逆转录定量实时PCR在六个分化条件下分析这些潜在参考基因的稳定性。结果通过微阵列分析GDNF和NGF诱导PC12细胞分化的基因,筛选出20个稳定表达的基因,包括13个核糖体蛋白基因。通过逆转录定量实时PCR进一步分析了这些候选基因以及ACTB和GAPDH在PC12细胞中的表达水平,所述PC12细胞分化为多种刺激物,包括NGF,GDNF,Forskolin,KCl和ROCK抑制剂Y27632。这些候选基因作为稳定参考基因的性能通过geNorm和NormFinder这两种独立的统计方法进行了评估。结论核糖体蛋白基因RPL19和RPL29被确定为PC12细胞神经元分化过程中的合适参考基因,而与分化条件的类型无关。这两个新的参考基因的组合,但不是常用的HKG GAPDH,可以在PC12分化过程中对差异表达基因进行稳健而准确的标准化。

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