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不同匹鲁卡品诱导的颞叶内侧癫痫模型中表达研究的合适内参基因的验证。

Validation of suitable reference genes for expression studies in different pilocarpine-induced models of mesial temporal lobe epilepsy.

机构信息

Department of Cell, Molecular Biology, Institute of Biological Sciences and Health, Federal University of Alagoas, AL, Brazil.

出版信息

PLoS One. 2013 Aug 23;8(8):e71892. doi: 10.1371/journal.pone.0071892. eCollection 2013.

Abstract

It is well recognized that the reference gene in a RT-qPCR should be properly validated to ensure that gene expression is unaffected by the experimental condition. We investigated eight potential reference genes in two different pilocarpine PILO-models of mesial temporal lobe epilepsy (MTLE) performing a stability expression analysis using geNorm, NormFinder and BestKepeer softwares. Then, as a validation strategy, we conducted a relative expression analysis of the Gfap gene. Our results indicate that in the systemic PILO-model Actb, Gapdh, Rplp1, Tubb2a and Polr1a mRNAs were highly stable in hippocampus of rats from all experimental and control groups, whereas Gusb revealed to be the most variable one. In fact, we observed that using Gusb for normalization, the relative mRNA levels of the Gfap gene differed from those obtained with stable genes. On the contrary, in the intrahippocampal PILO-model, all softwares included Gusb as a stable gene, whereas B2m was indicated as the worst candidate gene. The results obtained for the other reference genes were comparable to those observed for the systemic Pilo-model. The validation of these data by the analysis of the relative expression of Gfap showed that the upregulation of the Gfap gene in the hippocampus of rats sacrificed 24 hours after status epilepticus (SE) was undetected only when B2m was used as the normalizer. These findings emphasize that a gene that is stable in one pathology model may not be stable in a different experimental condition related to the same pathology and therefore, the choice of reference genes depends on study design.

摘要

众所周知,逆转录实时定量 PCR(RT-qPCR)中的参考基因应经过适当验证,以确保基因表达不受实验条件的影响。我们使用 geNorm、NormFinder 和 BestKeeper 软件对两种不同匹罗卡品诱导的颞叶内侧癫痫(MTLE)模型中的 8 个潜在参考基因进行了稳定性表达分析。然后,作为验证策略,我们对 Gfap 基因进行了相对表达分析。结果表明,在全身性匹罗卡品模型中,Actb、Gapdh、Rplp1、Tubb2a 和 Polr1a 的 mRNA 在来自所有实验组和对照组的大鼠海马中高度稳定,而 Gusb 则表现出最大的变异性。事实上,我们观察到,使用 Gusb 进行归一化,Gfap 基因的相对 mRNA 水平与使用稳定基因获得的水平不同。相反,在海马内匹罗卡品模型中,所有软件均将 Gusb 作为稳定基因,而 B2m 则被认为是最差的候选基因。其他参考基因的结果与全身性 Pilo 模型观察到的结果相似。通过分析 Gfap 的相对表达对这些数据进行验证表明,只有当 B2m 用作归一化时,才能检测到癫痫持续状态(SE)后 24 小时处死的大鼠海马中 Gfap 基因的上调。这些发现强调了在一种病理模型中稳定的基因在与同一病理相关的不同实验条件下可能不稳定,因此参考基因的选择取决于研究设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc3/3751890/854020753952/pone.0071892.g001.jpg

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