School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, Australia.
Alzheimers Dement. 2010 Nov;6(6):465-74. doi: 10.1016/j.jalz.2009.11.002.
Quantitative real-time reverse transcription-polymerase chain reaction (qRT-PCR) is a popular technique for mRNA expression studies. Normalization to an endogenous reference transcript (housekeeper) is widely used to correct for differences in loading and RNA quality. Alzheimer's disease (AD) alters brain metabolism. The stability of housekeeper transcript expression must be carefully validated.
qRT-PCR was used to assess eight putative housekeeper transcripts in four brain regions from 15 control, 12 AD, and 10 AD/Lewy body disease (LBD) cases.
RNA quality is lower in AD and AD/LBD than in controls. Frequently used housekeepers such as glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and β-actin had lower overall expression in AD and AD/LBD cases than in controls. RPL13 and 18S were the most stably expressed housekeepers tested. Synaptophysin and glial fibrillary acidic protein were used to evaluate normalized quantification. By using different housekeepers we confirmed that synaptophysin expression was down-regulated in AD cases, whereas glial fibrillary acidic protein expression was increased.
Among all candidates tested, RPL13 was the best housekeeper for qRT-PCR studies in autopsy brain tissue samples from controls and AD cases. RNA quality should be assessed and data normalized on this index as well.
实时荧光定量聚合酶链反应(qRT-PCR)是一种常用于研究 mRNA 表达的技术。内参基因(管家基因)的归一化广泛用于校正加载和 RNA 质量的差异。阿尔茨海默病(AD)会改变大脑代谢。管家基因转录本表达的稳定性必须经过仔细验证。
qRT-PCR 用于评估四个脑区的 15 个对照、12 个 AD 和 10 个 AD/LBD 病例中的 8 个潜在管家基因转录本。
AD 和 AD/LBD 的 RNA 质量低于对照组。经常使用的管家基因,如甘油醛-3-磷酸脱氢酶(GAPDH)和β-肌动蛋白,在 AD 和 AD/LBD 病例中的表达低于对照组。RPL13 和 18S 是测试中最稳定表达的管家基因。突触素和胶质纤维酸性蛋白用于评估归一化定量。通过使用不同的管家基因,我们证实突触素在 AD 病例中表达下调,而胶质纤维酸性蛋白表达增加。
在所有测试的候选基因中,RPL13 是用于对照和 AD 病例尸检脑组织样本 qRT-PCR 研究的最佳管家基因。也应该使用该指标评估 RNA 质量,并对数据进行归一化。