Tanic Nikola, Perovic Milka, Mladenovic Aleksandra, Ruzdijic Sabera, Kanazir Selma
Institute for Biological Research, Bul. Despota Stefana 142, 11 060 Belgrade, Serbia.
J Mol Neurosci. 2007;32(1):38-46. doi: 10.1007/s12031-007-0006-7.
Accurate normalization is the prerequisite for obtaining reliable results in the quantification of gene expression. Using TaqMan Real Time RT-PCR, we carried out an extensive evaluation of five most commonly used endogenous controls, gapdh, beta-actin, 18S rRNA, hprt and cypB, for their presumed stability of expression, in rat cortex and hippocampus, during aging, under dietary restriction and dexamethasone treatment. Valid reference genes (HKGs) were identified using GeNorm and NormFinder software packages and by direct comparison of Ct values. Analysis revealed gapdh and beta-actin as the most stable HKGs for all treatments analyzed, combined or separately, in the cortex, while in the hippocampus gapdh/hprt and beta-actin/hprt are the combination of choice for the single or combined effects of dietary restriction/dexamethasone, respectively. All treatments significantly influenced expression of 18S rRNA and cypB in both structures. In addition, we used gapdh and normalization factor, calculated by GeNorm, to compare the expression of alpha-syn in the cortex. Our results demonstrate the importance of the right choice of HKG and suggest the appropriate endogenous control to be used for TaqMan RT-PCR analysis of mRNA expression in rat cortex and hippocampus for selected experimental paradigms.
准确的标准化是在基因表达定量分析中获得可靠结果的前提条件。我们使用TaqMan实时逆转录聚合酶链反应(RT-PCR),对五种最常用的内参基因,即甘油醛-3-磷酸脱氢酶(gapdh)、β-肌动蛋白(beta-actin)、18S核糖体RNA(18S rRNA)、次黄嘌呤磷酸核糖转移酶(hprt)和细胞色素P450 2B1(cypB),在大鼠皮质和海马体中,于衰老过程中、饮食限制及地塞米松处理条件下,就其假定的表达稳定性进行了广泛评估。利用GeNorm和NormFinder软件包并通过直接比较Ct值来鉴定有效的参考基因(HKGs)。分析表明,在皮质中,对于所有分析的处理(合并或单独处理)而言,gapdh和beta-actin是最稳定的HKGs;而在海马体中,对于饮食限制/地塞米松的单一或联合作用,gapdh/hprt和beta-actin/hprt分别是首选的组合。所有处理均显著影响了这两种结构中18S rRNA和cypB的表达。此外,我们使用gapdh和由GeNorm计算得出的标准化因子,来比较皮质中α-突触核蛋白的表达。我们的结果证明了正确选择HKG的重要性,并为所选实验范式下大鼠皮质和海马体中mRNA表达的TaqMan RT-PCR分析建议了合适的内参基因。