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体内和体外培养的小鼠卵母细胞及胚胎中参考基因的定量评估与筛选

Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro.

作者信息

Mamo Solomon, Gal Arpad Baji, Bodo Szilard, Dinnyes Andras

机构信息

Genetic Reprogramming Group, Agricultural Biotechnology Center, Szent Gyorgyi Albert ut 4, H-2100 Gödöllo, Hungary.

出版信息

BMC Dev Biol. 2007 Mar 6;7:14. doi: 10.1186/1471-213X-7-14.

Abstract

BACKGROUND

Real-time PCR is an efficient tool to measure transcripts and provide valuable quantitative information on gene expression of preimplantation stage embryos. Finding valid reference genes for normalization is essential to interpret the real-time PCR results accurately, and understand the biological dynamics during early development. The use of reference genes also known as housekeeping genes is the most widely applied approach. However, the different genes are not systematically compared, and as a result there is no uniformity between studies in selecting the reference gene. The goals of this study were to compare a wide selection of the most commonly used housekeeping genes in mouse oocytes and preimplantation stage embryos produced under different culture conditions, and select the best stable genes for normalization of gene expression data.

RESULTS

Quantitative real time PCR method was used to evaluate 12 commonly used housekeeping genes (Actb, Gapdh, H2afz, Hprt, Ppia, Ubc, Eef1e1, Tubb4, Hist2h2aa1, Tbp, Bmp7, Polr2a) in multiple individual embryos representing six different developmental stages. The results were analysed, and stable genes were selected using the geNorm software. The expression pattern was almost similar despite differences in the culture system; however, the transcript levels were affected by culture conditions. The genes have showed various stabilities, and have been ranked accordingly.

CONCLUSION

Compared to earlier studies with similar objectives, we used a unique approach in analysing larger number of genes, comparing embryo samples derived in vivo or in vitro, analysing the expression in the early and late maternal to zygote transition periods separately, and using multiple individual embryos. Based on detailed quantification, pattern analyses and using the geNorm application, we found Ppia, H2afz and Hprt1 genes to be the most stable across the different stages and culture conditions, while Actb, the classical housekeeping gene, showed the least stability. We recommend the use of the geometric averages of those three genes for normalization in mouse preimplantation-stage gene expression studies.

摘要

背景

实时定量聚合酶链反应(Real-time PCR)是一种用于测量转录本并提供有关植入前阶段胚胎基因表达的有价值定量信息的有效工具。找到有效的内参基因进行标准化对于准确解释实时定量聚合酶链反应结果以及理解早期发育过程中的生物学动态至关重要。使用内参基因(也称为管家基因)是应用最广泛的方法。然而,不同基因之间未进行系统比较,因此在选择内参基因的研究之间缺乏一致性。本研究的目的是比较在不同培养条件下产生的小鼠卵母细胞和植入前阶段胚胎中广泛选择的最常用管家基因,并选择用于标准化基因表达数据的最佳稳定基因。

结果

采用定量实时聚合酶链反应方法评估了12个常用管家基因(Actb、Gapdh、H2afz、Hprt、Ppia、Ubc、Eef1e1、Tubb4、Hist2h2aa1、Tbp、Bmp7、Polr2a)在代表六个不同发育阶段的多个单个胚胎中的表达。对结果进行分析,并使用geNorm软件选择稳定基因。尽管培养系统存在差异,但表达模式几乎相似;然而,转录水平受培养条件影响。这些基因表现出不同的稳定性,并据此进行了排名。

结论

与早期具有相似目标的研究相比,我们采用了独特的方法,分析了更多数量的基因,比较了体内或体外来源的胚胎样本,分别分析了从母细胞到合子转变的早期和晚期的表达,并使用了多个单个胚胎。基于详细的定量、模式分析并使用geNorm应用程序,我们发现Ppia、H2afz和Hprt1基因在不同阶段和培养条件下最稳定,而经典管家基因Actb稳定性最差。我们建议在小鼠植入前阶段基因表达研究中使用这三个基因的几何平均值进行标准化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8551/1832186/0410331e6622/1471-213X-7-14-1.jpg

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