Institute for Research in Immunology and Cancer (IRIC), Université de Montreal, Montreal, Quebec, Canada.
PLoS One. 2013 Sep 17;8(9):e72884. doi: 10.1371/journal.pone.0072884. eCollection 2013.
Accurate quantification of gene expression by qRT-PCR relies on normalization against a consistently expressed control gene. However, control genes in common use often vary greatly between samples, especially in cancer. The advent of Next Generation Sequencing technology offers the possibility to better select control genes with the least cell to cell variability in steady state transcript levels. Here we analyze the transcriptomes of 55 leukemia samples to identify the most consistent genes. This list is enriched for components of the proteasome (ex. PSMA1) and spliceosome (ex. SF3B2), and also includes the translation initiation factor EIF4H, and many heterogeneous nuclear ribonucleoprotein genes (ex. HNRNPL). We have validated the consistency of our new control genes in 1933 cancer and normal tissues using publically available RNA-seq data, and their usefulness in qRT-PCR analysis is clearly demonstrated.
qRT-PCR 中通过内参基因进行基因表达的精确定量依赖于内参基因的一致性表达。然而,常用的内参基因在不同样本之间差异很大,尤其是在癌症中。新一代测序技术的出现提供了更好的选择内参基因的可能性,这些内参基因在稳定状态转录水平上的细胞间变异性最小。在这里,我们分析了 55 个白血病样本的转录组,以鉴定最一致的基因。这个列表富含蛋白酶体(例如 PSMA1)和剪接体(例如 SF3B2)的成分,还包括翻译起始因子 EIF4H 和许多异质核核糖核蛋白基因(例如 HNRNPL)。我们使用公开可用的 RNA-seq 数据在 1933 个癌症和正常组织中验证了我们新的内参基因的一致性,并且清楚地证明了它们在 qRT-PCR 分析中的有用性。