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ß-Actin and GAPDH housekeeping gene expression in asthmatic airways is variable and not suitable for normalising mRNA levels

机译:ß-肌动蛋白和GAPDH管家基因在哮喘气道中的表达是可变的不适用于使mRNA水平正常化

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摘要

>Background: The use of reverse transcription-polymerase chain reaction (RT-PCR) to measure mRNA levels has led to the common use of ß-actin and GAPDH housekeeping genes as denominators for comparison of samples. Expression of these genes is assumed to remain constant, so normalising for variations in processing and signal quantitation. However, it is well documented that ß-actin and GAPDH expression is upregulated with proliferation, activation, and differentiation. We hypothesised that airway samples which differ in their cellular profiles and activation status have different levels of expression of GAPDH and ß-actin. >Methods: The mRNA for ß-actin, GAPDH, and interleukin (IL)-2 was measured in bronchoalveolar lavage (BAL) fluid cells and endobronchial biopsy tissue by competitive RT-PCR in a cross sectional study of 26 normal controls and 92 asthmatic subjects. >Results: For both BAL fluid cells and biopsy tissue, asthmatics overall had reduced expression of GAPDH and ß-actin mRNA. In asthmatic subjects not using inhaled corticosteroids (ICS), GAPDH mRNA levels in both BAL fluid and biopsy tissue, and ß-actin mRNA in BAL fluid cells were 10 times lower than samples from both normal controls and from asthmatic subjects using ICS. ß-Actin mRNA in biopsy specimens showed the same pattern of expression, but asthmatic subjects not using ICS were not significantly different from those receiving ICS treatment. IL-2 mRNA levels did not differ between the subject or treatment groups but, when expressed as a ratio with ß-actin, significant differences were seen. >Conclusions: ß-Actin and GAPDH used as denominators of gene expression quantitation in asthma research can cause confounding. Housekeeping genes need careful validation before their use in such quantitative mRNA assays.
机译:>背景:使用逆转录聚合酶链反应(RT-PCR)来测量mRNA水平已导致β-肌动蛋白和GAPDH管家基因普遍用作比较样品的分母。假定这些基因的表达保持恒定,因此可以对处理和信号定量的变化进行归一化。但是,有充分的文献证明β-肌动蛋白和GAPDH表达随增殖,激活和分化而上调。我们假设细胞结构和激活状态不同的气道样品具有不同水平的GAPDH和β-肌动蛋白表达。 >方法:通过竞争性RT-PCR在支气管肺泡灌洗(BAL)液细胞和支气管内活检组织中测量ß-肌动蛋白,GAPDH和白介素(IL)-2的mRNA 26名正常对照组和92名哮喘受试者。 >结果:对于BAL液细胞和活检组织,哮喘患者总体上GAPDH和ß-actinmRNA的表达均降低。在未使用吸入皮质类固醇(ICS)的哮喘受试者中,BAL液和活检组织中的GAPDH mRNA水平以及BAL液细胞中的ß-actinmRNA均比正常对照和使用ICS的哮喘受试者的样品低10倍。活检标本中的β-肌动蛋白mRNA显示相同的表达模式,但未使用ICS的哮喘受试者与接受ICS治疗的受试者无显着差异。在受试者或治疗组之间,IL-2 mRNA的水平没有差异,但是当以与β-肌动蛋白的比率表示时,可以看到明显的差异。 >结论:ß-肌动蛋白和GAPDH在哮喘研究中用作基因表达定量的分母,可能会引起混淆。管家基因在用于此类定量mRNA分析之前需要仔细验证。

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